Male principal investigators (almost) don’t publish with women in ecology and zoology.

Male principal investigators (almost) don't publish with women in ecology and zoology.

Illustration of ladies in science drops considerably at every profession stage, from early scholar to senior investigator. Disparities in alternatives for girls to contribute to analysis metrics, akin to distinguished speaker occasions and authorship, have been reported in lots of fields in the united statesA. and Europe. Nevertheless, whether or not feminine illustration in scientific contributions differs in different areas, akin to Latin America, just isn’t nicely understood.

On this examine, with the intention to decide whether or not feminine authorship is influenced by gender or institutional location of the final (senior) creator or by subfield inside ecology, we gathered creator info from 6849 articles in ten ecological and zoological journals that publish analysis articles both in or out of Latin America. We discovered that feminine authorship has risen marginally since 2002 (27 to 31%), and varies amongst Latin American nations, however not between Latin America and different areas.

Final creator gender predicted feminine co-authorship throughout all journals and areas, as analysis teams led by ladies printed with over 60% feminine co-authors whereas these led by males printed with lower than 20% feminine co-authors. Our findings recommend that implicit biases and stereotype threats that girls face in male-led laboratories might be sources of feminine withdrawal and leaky pipelines in ecology and zoology. Accordingly, we encourage each PI to self-evaluate their lifetime share of feminine co-authors. Feminine position fashions and cultural shifts-especially by male senior authors-are essential for feminine retention and unbiased participation in science.

Time-Restricted Inquiry-Based mostly Studying Promotes Energetic Pupil Engagement in Undergraduate Zoology Laboratory.

Organizing a zoology laboratory for an undergraduate course is usually a problem, notably in a limited-resource setting, because of the huge number of matters to cowl and the restricted numbers of preserved specimens and everlasting slides. In zoology, the category construction typically takes the type of a lecture demonstration adopted by pattern exhibition stations. This setting typically fails to actively have interaction nearly all of college students in exploring the specimens.
Male principal investigators (almost) don't publish with women in ecology and zoology.
Right here we suggest another group of a zoology class lab format comprised of brief guided-inquiry, time-restricted lab stations, and a freely structured follow-up challenge meant to extend consideration and conceptual understanding of the lab matter. The lab is designed in two components: a 10-minute in-class rotation portion, the place small teams of scholars take turns investigating specimens following an teacher demonstration, and an after-class group project.
We carried out the technique for 2 years, and it’s clear that our method considerably elevated college students’ lively engagement within the class. The time-restricted scheme ensures all college students take part regardless of restricted assets, whereas the guided directions hold the scholars targeted on the subject. Moreover, the crew project portion, particularly the media creation facet, promoted teamwork amongst group members.

Domesticated Animals on Exhibit on the Museum of Comparative Zoology, 1900-1928.

In 1905 the Museum of Comparative Zoology at Harvard College started planning for a brand new domesticated animals exhibition in honor of the 100th anniversary of the beginning of its founder Louis Agassiz. The ensuing shows of variation and heredity in poultry, pigeons, rabbits, mice, and guinea pigs proved surprisingly common to museumgoers. A few of these specimens nonetheless exist within the museum’s storage services, particularly a collection of poultry donated by the biologist Charles B.
Davenport and an elaborate set of guinea pigs from the experimental evolutionist William E. Citadel. Situating these domesticated animal shows inside educational and common cultures of poultry fancying, animal breeding, and evolutionary science reveals how a nineteenth-century museum identified for its ties to anti-evolutionary rules tried to modernize its public reveals.

Evolutionary computation in zoology and ecology.

Evolutionary computational strategies have adopted attributes of pure choice and evolution to unravel issues in laptop science, engineering, and different fields. The strategy is rising in use in zoology and ecology. Evolutionary rules could also be merged with an agent-based modeling perspective to have particular person animals or different brokers compete. 4 essential classes are mentioned: genetic algorithms, evolutionary programming, genetic programming, and evolutionary methods. In evolutionary computation, a inhabitants is represented in a means that permits for an goal operate to be assessed that’s related to the issue of curiosity.
The poorest performing members are faraway from the inhabitants, and remaining members reproduce and could also be mutated. The health of the members is once more assessed, and the cycle continues till a stopping situation is met. Case research embody optimizing: egg form given completely different clutch sizes, mate choice, migration of wildebeest, birds, and elk, vulture foraging habits, algal bloom prediction, and species richness given vitality constraints. Different case research simulate the evolution of species and a method to challenge shifts in species ranges in response to a altering local weather that features competitors and phenotypic plasticity.

17-DMAG, Hydrochloride Salt, >98%

BC024-025 25mg Ask for price

17-DMAG, Hydrochloride Salt, >99%

BC024-100 100mg Ask for price

17-DMAG, Hydrochloride Salt, >99%

BC024-101 1g Ask for price

17-DMAG, Hydrochloride Salt, >99%

BC024-250 250mg Ask for price

OSU-03012, Hydrochloride Salt, >98%

BC061-005 5mg
EUR 375.6

OSU-03012, Hydrochloride Salt, >98%

BC061-025 25mg
EUR 634.8

Bile salt

BB0225 25g
EUR 95.5

Mannitol Salt

254027 PK20
EUR 13.68

Tetracycline, Hydrochloride

CH054 25 g
EUR 142.8

Tetracycline, Hydrochloride

CH055 100 g
EUR 204

Ciprofloxacin hydrochloride

C032-25G 25 g
EUR 199.2

Ciprofloxacin hydrochloride

C032-5G 5 g
EUR 74.4

Clindamycin Hydrochloride

C035-100MG 100 mg
EUR 243.6

Clindamycin Hydrochloride

C035-50MG 50 mg
EUR 152.4

Chlortetracycline Hydrochloride

C072-100G 100 g
EUR 376.8

Chlortetracycline Hydrochloride

C072-25G 25 g
EUR 157.2

Chlortetracycline Hydrochloride

C072-5G 5 g
EUR 78

Cefozopran Hydrochloride

C099-100MG 100 mg
EUR 300

Cysteamine hydrochloride

C212-25G 25 g
EUR 78

Cysteamine hydrochloride

C212-4x25G 4 x 25 g
EUR 154.8

Ceftiofur Hydrochloride

C228-1G 1 g
EUR 129.6

Ceftiofur Hydrochloride

C228-5G 5 g
EUR 387.6

Cefmenoxime Hydrochloride

C240-100MG 100mg
EUR 136.8

Cefmenoxime Hydrochloride

C240-500MG 500mg
EUR 334.8

Cinacalcet Hydrochloride

C242-100MG 100mg
EUR 513.6

Cinacalcet Hydrochloride

C242-10MG 10mg
EUR 94.8

Enrofloxacin hydrochloride

E007-100MG 100 mg
EUR 147.6

Enrofloxacin hydrochloride

E007-1G 1 g
EUR 776.4

Enrofloxacin hydrochloride

E007-500MG 500 mg
EUR 475.2

Erlotinib hydrochloride

E017-100MG 100 mg
EUR 136.8

Erlotinib hydrochloride

E017-1G 1 g
EUR 373.2

Pazopanib Hydrochloride

A8347-100 100 mg
EUR 268.8
Description: Pazopanib HCl is a receptor tyrosine kinase inhibitor that targets multiple kinases, including VEGFR1, VEGFR2, VEGFR3, PDGFR, FGFR, c-Kit, and c-Fms, with IC50s 10nM, 30nM, 47nM, 84nM, 74nM, 140nM, and 146nM respectively [1-3].

Pazopanib Hydrochloride

A8347-25 25 mg
EUR 129.6
Description: Pazopanib HCl is a receptor tyrosine kinase inhibitor that targets multiple kinases, including VEGFR1, VEGFR2, VEGFR3, PDGFR, FGFR, c-Kit, and c-Fms, with IC50s 10nM, 30nM, 47nM, 84nM, 74nM, 140nM, and 146nM respectively [1-3].

Pazopanib Hydrochloride

A8347-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: Pazopanib HCl is a receptor tyrosine kinase inhibitor that targets multiple kinases, including VEGFR1, VEGFR2, VEGFR3, PDGFR, FGFR, c-Kit, and c-Fms, with IC50s 10nM, 30nM, 47nM, 84nM, 74nM, 140nM, and 146nM respectively [1-3].

Pazopanib Hydrochloride

A8347-500 500 mg
EUR 727.2
Description: Pazopanib HCl is a receptor tyrosine kinase inhibitor that targets multiple kinases, including VEGFR1, VEGFR2, VEGFR3, PDGFR, FGFR, c-Kit, and c-Fms, with IC50s 10nM, 30nM, 47nM, 84nM, 74nM, 140nM, and 146nM respectively [1-3].

Pazopanib Hydrochloride

A8347-S Evaluation Sample
EUR 97.2
Description: Pazopanib HCl is a receptor tyrosine kinase inhibitor that targets multiple kinases, including VEGFR1, VEGFR2, VEGFR3, PDGFR, FGFR, c-Kit, and c-Fms, with IC50s 10nM, 30nM, 47nM, 84nM, 74nM, 140nM, and 146nM respectively [1-3].

Bestatin hydrochloride

A8621-10 10 mg
EUR 157.2
Description: Bestatin hydrochloride, also known as Ubenimex, is an inhibitor of aminopeptidase B and N (APN)/CD13 [1].Bestatin, an antibiotic of microbial origin, is a potent inhibitor of some aminopeptidases which can be administered to cultured cells, intact animals and humans with low toxicity.

Bestatin hydrochloride

A8621-100 100 mg
EUR 532.8
Description: Bestatin hydrochloride, also known as Ubenimex, is an inhibitor of aminopeptidase B and N (APN)/CD13 [1].Bestatin, an antibiotic of microbial origin, is a potent inhibitor of some aminopeptidases which can be administered to cultured cells, intact animals and humans with low toxicity.

Bestatin hydrochloride

A8621-25 25 mg
EUR 226.8
Description: Bestatin hydrochloride, also known as Ubenimex, is an inhibitor of aminopeptidase B and N (APN)/CD13 [1].Bestatin, an antibiotic of microbial origin, is a potent inhibitor of some aminopeptidases which can be administered to cultured cells, intact animals and humans with low toxicity.

Bestatin hydrochloride

A8621-5 5 mg
EUR 129.6
Description: Bestatin hydrochloride, also known as Ubenimex, is an inhibitor of aminopeptidase B and N (APN)/CD13 [1].Bestatin, an antibiotic of microbial origin, is a potent inhibitor of some aminopeptidases which can be administered to cultured cells, intact animals and humans with low toxicity.

Flavopiridol hydrochloride

A8640-10 10 mg
EUR 129.6
Description: Flavopiridol hydrochloride is a selective inhibitor of CDK1, CDK2, CDK4 and CDK6 with IC50 value all ~41 nM as well as CDK7 with 300nM [1] [2] [3].CDKs are protein kinase families which involve in the process of regulating transcription, mRNA processing, cell differentiation and cell cycle.

Flavopiridol hydrochloride

A8640-100 100 mg
EUR 528
Description: Flavopiridol hydrochloride is a selective inhibitor of CDK1, CDK2, CDK4 and CDK6 with IC50 value all ~41 nM as well as CDK7 with 300nM [1] [2] [3].CDKs are protein kinase families which involve in the process of regulating transcription, mRNA processing, cell differentiation and cell cycle.

Flavopiridol hydrochloride

A8640-1000 1 g
EUR 3259.2
Description: Flavopiridol hydrochloride is a selective inhibitor of CDK1, CDK2, CDK4 and CDK6 with IC50 value all ~41 nM as well as CDK7 with 300nM [1] [2] [3].CDKs are protein kinase families which involve in the process of regulating transcription, mRNA processing, cell differentiation and cell cycle.

Flavopiridol hydrochloride

A8640-25 25 mg
EUR 199.2
Description: Flavopiridol hydrochloride is a selective inhibitor of CDK1, CDK2, CDK4 and CDK6 with IC50 value all ~41 nM as well as CDK7 with 300nM [1] [2] [3].CDKs are protein kinase families which involve in the process of regulating transcription, mRNA processing, cell differentiation and cell cycle.

Flavopiridol hydrochloride

A8640-5.1 10 mM (in 1mL DMSO)
EUR 129.6
Description: Flavopiridol hydrochloride is a selective inhibitor of CDK1, CDK2, CDK4 and CDK6 with IC50 value all ~41 nM as well as CDK7 with 300nM [1] [2] [3].CDKs are protein kinase families which involve in the process of regulating transcription, mRNA processing, cell differentiation and cell cycle.

Regorafenib hydrochloride

A3750-10 10 mg
EUR 150
Description: Regorafenib (BAY 73-4506) is a multikinase inhibitor with IC50 of 17, 40 and 69 nM c-KIT, VEGFR2, B-Raf.

Regorafenib hydrochloride

A3750-100 100 mg
EUR 282
Description: Regorafenib (BAY 73-4506) is a multikinase inhibitor with IC50 of 17, 40 and 69 nM c-KIT, VEGFR2, B-Raf.

Regorafenib hydrochloride

A3750-200 200 mg
EUR 582
Description: Regorafenib (BAY 73-4506) is a multikinase inhibitor with IC50 of 17, 40 and 69 nM c-KIT, VEGFR2, B-Raf.

Regorafenib hydrochloride

A3750-5.1 10 mM (in 1mL DMSO)
EUR 199.2
Description: Regorafenib (BAY 73-4506) is a multikinase inhibitor with IC50 of 17, 40 and 69 nM c-KIT, VEGFR2, B-Raf.

Regorafenib hydrochloride

A3750-50 50 mg
EUR 199.2
Description: Regorafenib (BAY 73-4506) is a multikinase inhibitor with IC50 of 17, 40 and 69 nM c-KIT, VEGFR2, B-Raf.

Resminostat hydrochloride

A3755-10 10 mg
EUR 428.4
Description: Resminostat is an inhibitor of histone deacetylase (HDAC) with IC50 values of 42.5nM, 50.1nM and 71.8nM, respectively against HDAC1, 3 and 6 [1].

Resminostat hydrochloride

A3755-100 100 mg
EUR 1905.6
Description: Resminostat is an inhibitor of histone deacetylase (HDAC) with IC50 values of 42.5nM, 50.1nM and 71.8nM, respectively against HDAC1, 3 and 6 [1].

Resminostat hydrochloride

A3755-5.1 10 mM (in 1mL DMSO)
EUR 464.4
Description: Resminostat is an inhibitor of histone deacetylase (HDAC) with IC50 values of 42.5nM, 50.1nM and 71.8nM, respectively against HDAC1, 3 and 6 [1].

Resminostat hydrochloride

A3755-50 50 mg
EUR 1209.6
Description: Resminostat is an inhibitor of histone deacetylase (HDAC) with IC50 values of 42.5nM, 50.1nM and 71.8nM, respectively against HDAC1, 3 and 6 [1].

Rimonabant hydrochloride

A3766-10 10 mg
EUR 186
Description: Rimonabant, also known as SR141716, was the first selective central cannabinoid (CB1) receptor inverse agonist (Ki = 1.8 nM) to be developed as an appetite suppressant, anti-obesity drug.

Rimonabant hydrochloride

A3766-100 100 mg
EUR 710.4
Description: Rimonabant, also known as SR141716, was the first selective central cannabinoid (CB1) receptor inverse agonist (Ki = 1.8 nM) to be developed as an appetite suppressant, anti-obesity drug.

Rimonabant hydrochloride

A3766-5.1 10 mM (in 1mL DMSO)
EUR 199.2
Description: Rimonabant, also known as SR141716, was the first selective central cannabinoid (CB1) receptor inverse agonist (Ki = 1.8 nM) to be developed as an appetite suppressant, anti-obesity drug.

Rimonabant hydrochloride

A3766-50 50 mg
EUR 494.4
Description: Rimonabant, also known as SR141716, was the first selective central cannabinoid (CB1) receptor inverse agonist (Ki = 1.8 nM) to be developed as an appetite suppressant, anti-obesity drug.

Rotigotine hydrochloride

A3777-100 100 mg
EUR 480
Description: Rotigotine is dopamine D2 and D3 receptor agonist. Ki values are 13 and 0.71 nM for D2 and D3 respectively. Rotigotine also has significant affinity for 5-HT1A and adrenergic ?2B receptors. Rotigotine exhibits antiparkinsonian acitivity.

Rotigotine hydrochloride

A3777-200 200 mg
EUR 812.4
Description: Rotigotine is dopamine D2 and D3 receptor agonist. Ki values are 13 and 0.71 nM for D2 and D3 respectively. Rotigotine also has significant affinity for 5-HT1A and adrenergic ?2B receptors. Rotigotine exhibits antiparkinsonian acitivity.

Rotigotine hydrochloride

A3777-5.1 10 mM (in 1mL DMSO)
EUR 417.6
Description: Rotigotine is dopamine D2 and D3 receptor agonist. Ki values are 13 and 0.71 nM for D2 and D3 respectively. Rotigotine also has significant affinity for 5-HT1A and adrenergic ?2B receptors. Rotigotine exhibits antiparkinsonian acitivity.

Rotigotine hydrochloride

A3777-50 50 mg
EUR 360
Description: Rotigotine is dopamine D2 and D3 receptor agonist. Ki values are 13 and 0.71 nM for D2 and D3 respectively. Rotigotine also has significant affinity for 5-HT1A and adrenergic ?2B receptors. Rotigotine exhibits antiparkinsonian acitivity.

Rotigotine hydrochloride

A3777-500 500 mg
EUR 1663.2
Description: Rotigotine is dopamine D2 and D3 receptor agonist. Ki values are 13 and 0.71 nM for D2 and D3 respectively. Rotigotine also has significant affinity for 5-HT1A and adrenergic ?2B receptors. Rotigotine exhibits antiparkinsonian acitivity.

Tipiracil hydrochloride

A3875-10 10 mg
EUR 553.2
Description: Tipiracil is an inhibitor of Thymidine phosphorylase (TP). Thymidine phosphorylase (TP)is a key enzyme in the pyrimidine nucleoside salvage pathway.

Tipiracil hydrochloride

A3875-25 25 mg
EUR 774
Description: Tipiracil is an inhibitor of Thymidine phosphorylase (TP). Thymidine phosphorylase (TP)is a key enzyme in the pyrimidine nucleoside salvage pathway.

Tipiracil hydrochloride

A3875-5 5 mg
EUR 382.8
Description: Tipiracil is an inhibitor of Thymidine phosphorylase (TP). Thymidine phosphorylase (TP)is a key enzyme in the pyrimidine nucleoside salvage pathway.

Tipiracil hydrochloride

A3875-5.1 10 mM (in 1mL DMSO)
EUR 351.6
Description: Tipiracil is an inhibitor of Thymidine phosphorylase (TP). Thymidine phosphorylase (TP)is a key enzyme in the pyrimidine nucleoside salvage pathway.

Tipiracil hydrochloride

A3875-50 50 mg
EUR 1230
Description: Tipiracil is an inhibitor of Thymidine phosphorylase (TP). Thymidine phosphorylase (TP)is a key enzyme in the pyrimidine nucleoside salvage pathway.

Vandetanib hydrochloride

A3906-100 100 mg
EUR 517.2
Description: Description: IC50 Value: 40 nM (VEGFR2) [1]; 500 nM (EGFR) [2] Vandetanib is an anti-cancer drug that is used for the treatment of certain tumours of thethyroid gland.

Vandetanib hydrochloride

A3906-25 25 mg
EUR 201.6
Description: Description: IC50 Value: 40 nM (VEGFR2) [1]; 500 nM (EGFR) [2] Vandetanib is an anti-cancer drug that is used for the treatment of certain tumours of thethyroid gland.

Vernakalant Hydrochloride

A3915-10 10 mg
EUR 847.2
Description: IC50: Vernakalant inhibits two specific potassium currents, IKur (IC50 = 9 ??) and IKACh (IC50=10 ?M) which are only present in atrial myocardium [1].Vernakalant blocks atrial potassium channels, thereby prolonging repolarization.

Vernakalant Hydrochloride

A3915-100 100 mg
EUR 3316.8
Description: IC50: Vernakalant inhibits two specific potassium currents, IKur (IC50 = 9 ??) and IKACh (IC50=10 ?M) which are only present in atrial myocardium [1].Vernakalant blocks atrial potassium channels, thereby prolonging repolarization.

Vernakalant Hydrochloride

A3915-50 50 mg
EUR 2090.4
Description: IC50: Vernakalant inhibits two specific potassium currents, IKur (IC50 = 9 ??) and IKACh (IC50=10 ?M) which are only present in atrial myocardium [1].Vernakalant blocks atrial potassium channels, thereby prolonging repolarization.

Vilazodone Hydrochloride

A3919-10 10 mg
EUR 129.6
Description: Vilazodone (EMD 68843; SB 659746A; 5-{4-[4-(5-cyano-3-indolyl)-butyl]-1-piperazinyl}-benzofuran-2-carboxamide hydrochloride) is a combined serotonin specific reuptake inhibitor (SSRI) and 5-HT1A receptor partial agonist currently under clinical evaluation for the treatment of major depression.

Vilazodone Hydrochloride

A3919-5.1 10 mM (in 1mL DMSO)
EUR 129.6
Description: Vilazodone (EMD 68843; SB 659746A; 5-{4-[4-(5-cyano-3-indolyl)-butyl]-1-piperazinyl}-benzofuran-2-carboxamide hydrochloride) is a combined serotonin specific reuptake inhibitor (SSRI) and 5-HT1A receptor partial agonist currently under clinical evaluation for the treatment of major depression.

Vilazodone Hydrochloride

A3919-50 50 mg
EUR 157.2
Description: Vilazodone (EMD 68843; SB 659746A; 5-{4-[4-(5-cyano-3-indolyl)-butyl]-1-piperazinyl}-benzofuran-2-carboxamide hydrochloride) is a combined serotonin specific reuptake inhibitor (SSRI) and 5-HT1A receptor partial agonist currently under clinical evaluation for the treatment of major depression.

Voreloxin Hydrochloride

A3925-10 10 mg
EUR 895.2
Description: Voreloxin is a small molecule and a naphthyridine analogue with antineoplastic activity. Vosaroxin intercalates into DNA in a site-specific manner and blocks the re-ligation process carried out by topoisomerase II during DNA replication.

Voreloxin Hydrochloride

A3925-5 5 mg
EUR 656.4
Description: Voreloxin is a small molecule and a naphthyridine analogue with antineoplastic activity. Vosaroxin intercalates into DNA in a site-specific manner and blocks the re-ligation process carried out by topoisomerase II during DNA replication.

Voreloxin Hydrochloride

A3925-5.1 10 mM (in 1mL DMSO)
EUR 717.6
Description: Voreloxin is a small molecule and a naphthyridine analogue with antineoplastic activity. Vosaroxin intercalates into DNA in a site-specific manner and blocks the re-ligation process carried out by topoisomerase II during DNA replication.

PJ34 hydrochloride

A4159-10 10 mg
EUR 142.8
Description: PJ34 is a novel and potent inhibitor of poly(ADP-ribose) polymerase (PARP), an enzyme involved in DNA repair and cell proliferation, that dose-dependently inhibits purified PARP enzyme in a cell-free assay with half maximal effective concentration EC50 value of 20 nM.

PJ34 hydrochloride

A4159-5 5 mg
EUR 129.6
Description: PJ34 is a novel and potent inhibitor of poly(ADP-ribose) polymerase (PARP), an enzyme involved in DNA repair and cell proliferation, that dose-dependently inhibits purified PARP enzyme in a cell-free assay with half maximal effective concentration EC50 value of 20 nM.

PJ34 hydrochloride

A4159-5.1 10 mM (in 1mL DMSO)
EUR 150
Description: PJ34 is a novel and potent inhibitor of poly(ADP-ribose) polymerase (PARP), an enzyme involved in DNA repair and cell proliferation, that dose-dependently inhibits purified PARP enzyme in a cell-free assay with half maximal effective concentration EC50 value of 20 nM.

PJ34 hydrochloride

A4159-50 50 mg
EUR 296.4
Description: PJ34 is a novel and potent inhibitor of poly(ADP-ribose) polymerase (PARP), an enzyme involved in DNA repair and cell proliferation, that dose-dependently inhibits purified PARP enzyme in a cell-free assay with half maximal effective concentration EC50 value of 20 nM.

PJ34 hydrochloride

A4159-S Evaluation Sample
EUR 97.2
Description: PJ34 is a novel and potent inhibitor of poly(ADP-ribose) polymerase (PARP), an enzyme involved in DNA repair and cell proliferation, that dose-dependently inhibits purified PARP enzyme in a cell-free assay with half maximal effective concentration EC50 value of 20 nM.

Dimethylamine hydrochloride

DB0410 500g
EUR 116.38

Daunorubicin hydrochloride

D001-10MG 10 mg
EUR 142.8

Daunorubicin hydrochloride

D001-50MG 50 mg
EUR 480

Difloxacin hydrochloride

D021-1G 1 g
EUR 133.2

Difloxacin hydrochloride

D021-5G 5 g
EUR 438

Demeclocycline hydrochloride

D032-1G 1 g
EUR 208.8

Demeclocycline hydrochloride

D032-250MG 250 mg
EUR 105.6

Demeclocycline hydrochloride

D032-5G 5 g
EUR 646.8

Doxycycline Hydrochloride

D065-25MG 25mg
EUR 410.4

Doxycycline Hydrochloride

D065-5MG 5mg
EUR 142.8

Dalbavancin Hydrochloride

D092-10MG 10mg
EUR 152.4

Dalbavancin Hydrochloride

D092-50MG 50mg
EUR 456

Cefepime Hydrochloride

C009-100MG 100 mg
EUR 320.4

Ceftazidime Hydrochloride

C020-1G 1 g
EUR 746.4

Niguldipine (hydrochloride)

C3067-10 10 mg
EUR 164.4
Description: Ki = 0.16 nM: ?1A-adrenoceptor antagonistIC50s = 0.4 ?M: inhibits L-type Ca2+ channelsIC50s = 0.9 ?M: suppresses T-type Ca2+ channelsNiguldipine is a less potent Ca2+ channel blocker and potent, selective ?1A-adrenoceptor receptor antagonist.

Niguldipine (hydrochloride)

C3067-25 25 mg
EUR 308.4
Description: Ki = 0.16 nM: ?1A-adrenoceptor antagonistIC50s = 0.4 ?M: inhibits L-type Ca2+ channelsIC50s = 0.9 ?M: suppresses T-type Ca2+ channelsNiguldipine is a less potent Ca2+ channel blocker and potent, selective ?1A-adrenoceptor receptor antagonist.

AD57 (hydrochloride)

C3080-1 1 mg
EUR 141.6
Description: IC50: 2 nM: blocks the receptor tyrosine kinase RET in Drosophila.AD57, as a polypharmacological cancer therapeutic, is designed to regulate multiple targets related to cancer.

AD57 (hydrochloride)

C3080-10 10 mg
EUR 714
Description: IC50: 2 nM: blocks the receptor tyrosine kinase RET in Drosophila.AD57, as a polypharmacological cancer therapeutic, is designed to regulate multiple targets related to cancer.

AD57 (hydrochloride)

C3080-5 5 mg
EUR 428.4
Description: IC50: 2 nM: blocks the receptor tyrosine kinase RET in Drosophila.AD57, as a polypharmacological cancer therapeutic, is designed to regulate multiple targets related to cancer.

Pargyline (hydrochloride)

C3106-1000 1 g
EUR 139.2
Description: IC50: 11.52 nM: inhibits monoamine oxidase (MAO) type A (MAO-A).IC50: 8.2 nM: blocks MAO type B (MAO-B).Pargyline, an irreversible and non-selective inhibitor of MAO, is used to treat moderate hypertension and cancer cells.

Pargyline (hydrochloride)

C3106-5000 5 g
EUR 410.4
Description: IC50: 11.52 nM: inhibits monoamine oxidase (MAO) type A (MAO-A).IC50: 8.2 nM: blocks MAO type B (MAO-B).Pargyline, an irreversible and non-selective inhibitor of MAO, is used to treat moderate hypertension and cancer cells.

Clenbuterol (hydrochloride)

C3119-100 100 mg
EUR 258
Description: Clenbuterol is a sympathomimetic ?2-adrenoceptor agonist. ?2-adrenoceptor agonists, mainly long-acting ?2-adrenoceptor agonists, are an important pharmacological approach to induce bronchodilation in patients with chronic obstructive pulmonary disease.

Clenbuterol (hydrochloride)

C3119-25 25 mg
EUR 130.8
Description: Clenbuterol is a sympathomimetic ?2-adrenoceptor agonist. ?2-adrenoceptor agonists, mainly long-acting ?2-adrenoceptor agonists, are an important pharmacological approach to induce bronchodilation in patients with chronic obstructive pulmonary disease.

Clenbuterol (hydrochloride)

C3119-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: Clenbuterol is a sympathomimetic ?2-adrenoceptor agonist. ?2-adrenoceptor agonists, mainly long-acting ?2-adrenoceptor agonists, are an important pharmacological approach to induce bronchodilation in patients with chronic obstructive pulmonary disease.

Clenbuterol (hydrochloride)

C3119-50 50 mg
EUR 189.6
Description: Clenbuterol is a sympathomimetic ?2-adrenoceptor agonist. ?2-adrenoceptor agonists, mainly long-acting ?2-adrenoceptor agonists, are an important pharmacological approach to induce bronchodilation in patients with chronic obstructive pulmonary disease.

CBL0137 (hydrochloride)

C3192-10 10 mg
EUR 529.2
Description: EC50: 0.37 ?M for activating p53; 0.47 ?M for inhibiting NF-?B CBL0137 (hydrochloride) is a curaxin that activates p53 and inhibits NF-?B.

CBL0137 (hydrochloride)

C3192-25 25 mg
EUR 1071.6
Description: EC50: 0.37 ?M for activating p53; 0.47 ?M for inhibiting NF-?B CBL0137 (hydrochloride) is a curaxin that activates p53 and inhibits NF-?B.

CBL0137 (hydrochloride)

C3192-5 5 mg
EUR 331.2
Description: EC50: 0.37 ?M for activating p53; 0.47 ?M for inhibiting NF-?B CBL0137 (hydrochloride) is a curaxin that activates p53 and inhibits NF-?B.

CBL0137 (hydrochloride)

C3192-5.1 10 mM (in 1mL DMSO)
EUR 282
Description: EC50: 0.37 ?M for activating p53; 0.47 ?M for inhibiting NF-?B CBL0137 (hydrochloride) is a curaxin that activates p53 and inhibits NF-?B.

CBL0137 (hydrochloride)

C3192-50 50 mg
EUR 1851.6
Description: EC50: 0.37 ?M for activating p53; 0.47 ?M for inhibiting NF-?B CBL0137 (hydrochloride) is a curaxin that activates p53 and inhibits NF-?B.

CPTH2 (hydrochloride)

C3208-10 10 mg
EUR 231.6
Description: CPTH2 is an inhibitor of HAT activity of Gcn5.

CPTH2 (hydrochloride)

C3208-5 5 mg
EUR 192
Description: CPTH2 is an inhibitor of HAT activity of Gcn5.

Clinafloxacin (hydrochloride)

C3345-100 100 mg
EUR 184.8
Description: Clinafloxacin is a broad-spectrum antibiotic of the quinolone carboxylic acid category that inhibits both DNA gyrase and topoisomerase IV dually in Streptococcus pneumonia. Clinafloxacin, a fluoroquinolone, is currently in development for oral and intravenous therapy of serious infections.

Clinafloxacin (hydrochloride)

C3345-1000 1 g
EUR 686.4
Description: Clinafloxacin is a broad-spectrum antibiotic of the quinolone carboxylic acid category that inhibits both DNA gyrase and topoisomerase IV dually in Streptococcus pneumonia. Clinafloxacin, a fluoroquinolone, is currently in development for oral and intravenous therapy of serious infections.

Clinafloxacin (hydrochloride)

C3345-250 250 mg
EUR 309.6
Description: Clinafloxacin is a broad-spectrum antibiotic of the quinolone carboxylic acid category that inhibits both DNA gyrase and topoisomerase IV dually in Streptococcus pneumonia. Clinafloxacin, a fluoroquinolone, is currently in development for oral and intravenous therapy of serious infections.

Clinafloxacin (hydrochloride)

C3345-500 500 mg
EUR 459.6
Description: Clinafloxacin is a broad-spectrum antibiotic of the quinolone carboxylic acid category that inhibits both DNA gyrase and topoisomerase IV dually in Streptococcus pneumonia. Clinafloxacin, a fluoroquinolone, is currently in development for oral and intravenous therapy of serious infections.

Isoxsuprine (hydrochloride)

C3347-10000 10 g
EUR 145.2
Description: Isoxsuprine is a modulator of ?2 adrenoreceptor and has agonist or antagonist effects.The ?2 adrenoceptors are a class of G protein-coupled receptors that are targets for epinephrine.

Isoxsuprine (hydrochloride)

C3347-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: Isoxsuprine is a modulator of ?2 adrenoreceptor and has agonist or antagonist effects.The ?2 adrenoceptors are a class of G protein-coupled receptors that are targets for epinephrine.

DAPI (hydrochloride)

C3362-10 10 mg
EUR 146.4

DAPI (hydrochloride)

C3362-25 25 mg
EUR 240

DAPI (hydrochloride)

C3362-5 5 mg
EUR 111.6

Kanosamine (hydrochloride)

C3461-10 10 mg
EUR 528
Description: Kanosamine is the antibiotic produced by Bacillus cereus UW85. Kanosamine showed highly inhibitory effects to the growth of plant-pathogenic oomycetes and moderately inhibitory effects to certain fungi and inhibited few bacterial species tested.

Kanosamine (hydrochloride)

C3461-25 25 mg
EUR 1089.6
Description: Kanosamine is the antibiotic produced by Bacillus cereus UW85. Kanosamine showed highly inhibitory effects to the growth of plant-pathogenic oomycetes and moderately inhibitory effects to certain fungi and inhibited few bacterial species tested.

Kanosamine (hydrochloride)

C3461-5 5 mg
EUR 324
Description: Kanosamine is the antibiotic produced by Bacillus cereus UW85. Kanosamine showed highly inhibitory effects to the growth of plant-pathogenic oomycetes and moderately inhibitory effects to certain fungi and inhibited few bacterial species tested.

Zoniporide (hydrochloride)

C3480-10 10 mg
EUR 278.4
Description: Zoniporide (hydrochloride) is a novel, potent, and selective sodium-hydrogen exchanger isoform-1 (NHE-1) inhibitor [1]. The Na+/H+ exchanger (NHE) has been involved in intracellular pH homeostasis of many mammalian cell types.

Zoniporide (hydrochloride)

C3480-5 5 mg
EUR 181.2
Description: Zoniporide (hydrochloride) is a novel, potent, and selective sodium-hydrogen exchanger isoform-1 (NHE-1) inhibitor [1]. The Na+/H+ exchanger (NHE) has been involved in intracellular pH homeostasis of many mammalian cell types.

Zoniporide (hydrochloride)

C3480-50 50 mg
EUR 1004.4
Description: Zoniporide (hydrochloride) is a novel, potent, and selective sodium-hydrogen exchanger isoform-1 (NHE-1) inhibitor [1]. The Na+/H+ exchanger (NHE) has been involved in intracellular pH homeostasis of many mammalian cell types.

MS023 (hydrochloride)

C3503-1 1 mg
EUR 134.4
Description: IC50: 20, 119, 83, 8, and 8 nM for PRMT1, 3, 4, 6, and 8, respectivelyMS023 is a type I PRMT inhibitor. Protein arginine methyltransferases (PRMTs) play a critical role in various biological processes.

MS023 (hydrochloride)

C3503-10 10 mg
EUR 661.2
Description: IC50: 20, 119, 83, 8, and 8 nM for PRMT1, 3, 4, 6, and 8, respectivelyMS023 is a type I PRMT inhibitor. Protein arginine methyltransferases (PRMTs) play a critical role in various biological processes.

MS023 (hydrochloride)

C3503-25 25 mg
EUR 1375.2
Description: IC50: 20, 119, 83, 8, and 8 nM for PRMT1, 3, 4, 6, and 8, respectivelyMS023 is a type I PRMT inhibitor. Protein arginine methyltransferases (PRMTs) play a critical role in various biological processes.

MS023 (hydrochloride)

C3503-5 5 mg
EUR 398.4
Description: IC50: 20, 119, 83, 8, and 8 nM for PRMT1, 3, 4, 6, and 8, respectivelyMS023 is a type I PRMT inhibitor. Protein arginine methyltransferases (PRMTs) play a critical role in various biological processes.

Chlorprothixene (hydrochloride)

C3509-1000 1 g
EUR 103.2
Description: Chlorprothixene (hydrochloride) is an antagonist of dopamine receptor and histamine receptors [1]. Chlorprothixene is also an inhibitor of GABAA receptor [2]. All of these three receptors are implicated in many neurological processes, including motivation, pleasure, cognition, memory and learning.

Chlorprothixene (hydrochloride)

C3509-10000 10 g
EUR 397.2
Description: Chlorprothixene (hydrochloride) is an antagonist of dopamine receptor and histamine receptors [1]. Chlorprothixene is also an inhibitor of GABAA receptor [2]. All of these three receptors are implicated in many neurological processes, including motivation, pleasure, cognition, memory and learning.

Chlorprothixene (hydrochloride)

C3509-25000 25 g
EUR 796.8
Description: Chlorprothixene (hydrochloride) is an antagonist of dopamine receptor and histamine receptors [1]. Chlorprothixene is also an inhibitor of GABAA receptor [2]. All of these three receptors are implicated in many neurological processes, including motivation, pleasure, cognition, memory and learning.

Chlorprothixene (hydrochloride)

C3509-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: Chlorprothixene (hydrochloride) is an antagonist of dopamine receptor and histamine receptors [1]. Chlorprothixene is also an inhibitor of GABAA receptor [2]. All of these three receptors are implicated in many neurological processes, including motivation, pleasure, cognition, memory and learning.

Chlorprothixene (hydrochloride)

C3509-5000 5 g
EUR 249.6
Description: Chlorprothixene (hydrochloride) is an antagonist of dopamine receptor and histamine receptors [1]. Chlorprothixene is also an inhibitor of GABAA receptor [2]. All of these three receptors are implicated in many neurological processes, including motivation, pleasure, cognition, memory and learning.

Cycloguanil (hydrochloride)

C5763-10 10 mg
EUR 130.8
Description: Cycloguanil is an inhibitor of dihydrofolate reductase (DHFR)[1].Dihydrofolate reductase (DHFR) is an enzyme that involved in reducing dihydrofolic acid to tetrahydrofolic acid.

Cycloguanil (hydrochloride)

C5763-25 25 mg
EUR 195.6
Description: Cycloguanil is an inhibitor of dihydrofolate reductase (DHFR)[1].Dihydrofolate reductase (DHFR) is an enzyme that involved in reducing dihydrofolic acid to tetrahydrofolic acid.

Cycloguanil (hydrochloride)

C5763-50 50 mg
EUR 247.2
Description: Cycloguanil is an inhibitor of dihydrofolate reductase (DHFR)[1].Dihydrofolate reductase (DHFR) is an enzyme that involved in reducing dihydrofolic acid to tetrahydrofolic acid.

Bufuralol (hydrochloride)

C5043-1 1 mg
EUR 166.8
Description: Bufuralol is a non-specific ?-adrenergic blocker. Beta adrenergic agonists are medications relaxing muscles of the airways, which widens the airways and leads to easier breathing.

Bufuralol (hydrochloride)

C5043-10 10 mg
EUR 753.6
Description: Bufuralol is a non-specific ?-adrenergic blocker. Beta adrenergic agonists are medications relaxing muscles of the airways, which widens the airways and leads to easier breathing.

Bufuralol (hydrochloride)

C5043-5 5 mg
EUR 548.4
Description: Bufuralol is a non-specific ?-adrenergic blocker. Beta adrenergic agonists are medications relaxing muscles of the airways, which widens the airways and leads to easier breathing.

AN3365 (hydrochloride)

C5068-10 10 mg
EUR 393.6
Description: AN3365 is a potent and selective leucyl-tRNA synthetase inhibitor [1].The leucyl-tRNA synthetase belongs to a member of the class I aminoacyl-tRNA synthetase family.

AN3365 (hydrochloride)

C5068-25 25 mg
EUR 790.8
Description: AN3365 is a potent and selective leucyl-tRNA synthetase inhibitor [1].The leucyl-tRNA synthetase belongs to a member of the class I aminoacyl-tRNA synthetase family.

AN3365 (hydrochloride)

C5068-5 5 mg
EUR 247.2
Description: AN3365 is a potent and selective leucyl-tRNA synthetase inhibitor [1].The leucyl-tRNA synthetase belongs to a member of the class I aminoacyl-tRNA synthetase family.

Calindol (hydrochloride)

C5329-10 10 mg
EUR 528
Description: Calindol is an activator of the calcium-sensing receptor (CaSR).The extracellular calciumsensing receptor (CaSR), a G protein-coupled receptor (GPCR), senses extracellular calcium[Ca2+]e and regulates calciumion homeostasis.

Calindol (hydrochloride)

C5329-25 25 mg
EUR 1082.4
Description: Calindol is an activator of the calcium-sensing receptor (CaSR).The extracellular calciumsensing receptor (CaSR), a G protein-coupled receptor (GPCR), senses extracellular calcium[Ca2+]e and regulates calciumion homeostasis.

Calindol (hydrochloride)

C5329-5 5 mg
EUR 324
Description: Calindol is an activator of the calcium-sensing receptor (CaSR).The extracellular calciumsensing receptor (CaSR), a G protein-coupled receptor (GPCR), senses extracellular calcium[Ca2+]e and regulates calciumion homeostasis.

Kasugamycin (hydrochloride)

C5503-10000 10 g
EUR 420
Description: Kasugamycin is an aminoglycosidic antibiotic. Aminoglycoside, a medicinal and bacteriologic category of traditional Gram-negative antibacterial therapeutic agent, inhibits protein synthesis and contains as a portion of the molecule an amino-modified glycoside.

Kasugamycin (hydrochloride)

C5503-5000 5 g
EUR 301.2
Description: Kasugamycin is an aminoglycosidic antibiotic. Aminoglycoside, a medicinal and bacteriologic category of traditional Gram-negative antibacterial therapeutic agent, inhibits protein synthesis and contains as a portion of the molecule an amino-modified glycoside.

Ciprofloxacin (hydrochloride)

C5539-10000 10 g
EUR 139.2
Description: Ciprofloxacin (hydrochloride) is a fluoroquinolone antibiotic that has antimicrobial and immunomodulatory activities [1].

Ciprofloxacin (hydrochloride)

C5539-25000 25 g
EUR 184.8
Description: Ciprofloxacin (hydrochloride) is a fluoroquinolone antibiotic that has antimicrobial and immunomodulatory activities [1].

Ciprofloxacin (hydrochloride)

C5539-50000 50 g
EUR 268.8
Description: Ciprofloxacin (hydrochloride) is a fluoroquinolone antibiotic that has antimicrobial and immunomodulatory activities [1].

Fendiline (hydrochloride)

C5675-5000 5 g
EUR 146.4
Description: Fendiline is an ?2-adrenergic receptor antagonist and L-type calcium channel blocker [1,2].The ?2 adrenergic receptor is a G protein-coupled receptor (GPCR). Until now, three different ?2-receptor subtypes have been identified: ?2A, ?2B, and ?2C.

Daunorubicin Hydrochloride

ADC-P-011 unit Ask for price

Doxorubicin hydrochloride

ADC-P-014 unit Ask for price

MMAD hydrochloride

ADC-P-019 unit Ask for price

MMAF Hydrochloride

ADC-P-021 unit Ask for price

Taltobulin hydrochloride

ADC-P-027 unit Ask for price

Moxifloxacin hydrochloride

E1KS1465 50mg
EUR 296.4

(±)-Salsolinol (hydrochloride)

C4364-500 500 mg
EUR 369.6
Description: (±)-Salsolinol targets depolarize dopamineric neurons. Dopaminergic neurons produce dopamine, a neurotransmitter with various roles in neurological functions.

Midodrine (hydrochloride)

C4493-100 100 mg
EUR 135.6
Description: Ki: 2, 6.9, and 1.7 ?M for ?1A, ?1B, ?1D, respectivelyMidodrine is the prodrug of the ?1-adrenergic receptor agonist, 1-(2?,5?-dimethoxyphenyl)-2-aminoethanol.
This introduction concludes by citing different makes use of of evolutionary computation and a assessment of the pliability of the strategies. For instance, representing species’ area of interest areas topic to selective strain permits research on cladistics, the taxon cycle, impartial versus area of interest paradigms, elementary versus realized niches, neighborhood construction and order of colonization, invasiveness, and responses to a altering local weather.

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