CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 100 of 865
Non-Antibody Products
Page 100 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Bialaphos (sodium salt) | A natural non-selective phytotoxin that is converted in vivo to the active… | 10 mg | 16754-10 | More Info |
| Bialaphos (sodium salt) | A natural non-selective phytotoxin that is converted in vivo to the active… | 100 mg | 16754-100 | More Info |
| Bialaphos (sodium salt) | A natural non-selective phytotoxin that is converted in vivo to the active… | 5 mg | 16754-5 | More Info |
| Bialaphos (sodium salt) | A natural non-selective phytotoxin that is converted in vivo to the active… | 50 mg | 16754-50 | More Info |
| Biapenem | A broad-spectrum β-lactam antibiotic; active against aerobic and anae… | 10 mg | 28822-10 | More Info |
| Biapenem | A broad-spectrum β-lactam antibiotic; active against aerobic and anae… | 100 mg | 28822-100 | More Info |
| Biapenem | A broad-spectrum β-lactam antibiotic; active against aerobic and anae… | 25 mg | 28822-25 | More Info |
| Biapenem | A broad-spectrum β-lactam antibiotic; active against aerobic and anae… | 50 mg | 28822-50 | More Info |
| 3,8'-Biapigenin | A biflavonoid with diverse biological activities; inhibits PTP1B (IC50 = 4… | 1 mg | 34143-1 | More Info |
| 3,8'-Biapigenin | A biflavonoid with diverse biological activities; inhibits PTP1B (IC50 = 4… | 5 mg | 34143-5 | More Info |
| BIBB 515 | A selective and potent inhibitor of 2,3-oxidosqualene cyclase (OSC) in viv… | 10 mg | 10010517-10 | More Info |
| BIBB 515 | A selective and potent inhibitor of 2,3-oxidosqualene cyclase (OSC) in viv… | 100 mg | 10010517-100 | More Info |
| BIBB 515 | A selective and potent inhibitor of 2,3-oxidosqualene cyclase (OSC) in viv… | 5 mg | 10010517-5 | More Info |
| BIBB 515 | A selective and potent inhibitor of 2,3-oxidosqualene cyclase (OSC) in viv… | 50 mg | 10010517-50 | More Info |
| BIBF 0775 | An ALK5 inhibitor (IC50 = 34 nM); selective for ALK5 over VEGFR2 and PDGFR… | 1 mg | 37777-1 | More Info |
| BIBF 0775 | An ALK5 inhibitor (IC50 = 34 nM); selective for ALK5 over VEGFR2 and PDGFR… | 10 mg | 37777-10 | More Info |
| BIBF 0775 | An ALK5 inhibitor (IC50 = 34 nM); selective for ALK5 over VEGFR2 and PDGFR… | 25 mg | 37777-25 | More Info |
| BIBF 0775 | An ALK5 inhibitor (IC50 = 34 nM); selective for ALK5 over VEGFR2 and PDGFR… | 5 mg | 37777-5 | More Info |
| BIBF 1120 | A VEGFR, FGFR, and PDGFR inhibitor (IC50s = 13-34, 37-610, 59, and 65 nM f… | 10 mg | 11022-10 | More Info |
| BIBF 1120 | A VEGFR, FGFR, and PDGFR inhibitor (IC50s = 13-34, 37-610, 59, and 65 nM f… | 100 mg | 11022-100 | More Info |
| BIBF 1120 | A VEGFR, FGFR, and PDGFR inhibitor (IC50s = 13-34, 37-610, 59, and 65 nM f… | 250 mg | 11022-250 | More Info |
| BIBF 1120 | A VEGFR, FGFR, and PDGFR inhibitor (IC50s = 13-34, 37-610, 59, and 65 nM f… | 50 mg | 11022-50 | More Info |
| BIBF 1202 | An active metabolite of BIBF 1120; inhibits VEGFR2 (IC50 = 62 nM) | 1 mg | 27176-1 | More Info |
| BIBF 1202 | An active metabolite of BIBF 1120; inhibits VEGFR2 (IC50 = 62 nM) | 10 mg | 27176-10 | More Info |
| BIBF 1202 | An active metabolite of BIBF 1120; inhibits VEGFR2 (IC50 = 62 nM) | 5 mg | 27176-5 | More Info |
| BIBF 1120-13C-d3 | An internal standard for the quantification of BIBF 1120 by GC- or LC-MS, | 1 mg | 25312-1 | More Info |
| BIBF 1120-13C-d3 | An internal standard for the quantification of BIBF 1120 by GC- or LC-MS, | 500 µg | 25312-500 | More Info |
| BIBF 1120 (esylate) | A VEGFR, FGFR, and PDGFR inhibitor (IC50s = 13-34, 37-610, 59, and 65 nM f… | 1 g | 31082-1 | More Info |
| BIBF 1120 (esylate) | A VEGFR, FGFR, and PDGFR inhibitor (IC50s = 13-34, 37-610, 59, and 65 nM f… | 100 mg | 31082-100 | More Info |
| BIBF 1120 (esylate) | A VEGFR, FGFR, and PDGFR inhibitor (IC50s = 13-34, 37-610, 59, and 65 nM f… | 50 mg | 31082-50 | More Info |
| BIBF 1120 (esylate) | A VEGFR, FGFR, and PDGFR inhibitor (IC50s = 13-34, 37-610, 59, and 65 nM f… | 500 mg | 31082-500 | More Info |
| BIBO-3304 (trifluoroacetate salt) | An antagonist of NPY receptor Y1 (Kis = 0.38 and 0.72 nM, respectively); s… | 1 mg | 35205-1 | More Info |
| BIBO-3304 (trifluoroacetate salt) | An antagonist of NPY receptor Y1 (Kis = 0.38 and 0.72 nM, respectively); s… | 10 mg | 35205-10 | More Info |
| BIBO-3304 (trifluoroacetate salt) | An antagonist of NPY receptor Y1 (Kis = 0.38 and 0.72 nM, respectively); s… | 25 mg | 35205-25 | More Info |
| BIBO-3304 (trifluoroacetate salt) | An antagonist of NPY receptor Y1 (Kis = 0.38 and 0.72 nM, respectively); s… | 5 mg | 35205-5 | More Info |
| BIBP3226 | A nonpeptide antagonist of NPY Y1 (Ki = 1.1 nM); selective for Y1 over Y2,… | 1 mg | 33210-1 | More Info |
| BIBP3226 | A nonpeptide antagonist of NPY Y1 (Ki = 1.1 nM); selective for Y1 over Y2,… | 10 mg | 33210-10 | More Info |
| BIBP3226 | A nonpeptide antagonist of NPY Y1 (Ki = 1.1 nM); selective for Y1 over Y2,… | 25 mg | 33210-25 | More Info |
| BIBP3226 | A nonpeptide antagonist of NPY Y1 (Ki = 1.1 nM); selective for Y1 over Y2,… | 5 mg | 33210-5 | More Info |
| BIBR 1532 | A mixed-type non-competitive inhibitor of telomerase (IC50 = 93 nM) that h… | 1 mg | 16608-1 | More Info |
| BIBR 1532 | A mixed-type non-competitive inhibitor of telomerase (IC50 = 93 nM) that h… | 10 mg | 16608-10 | More Info |
| BIBR 1532 | A mixed-type non-competitive inhibitor of telomerase (IC50 = 93 nM) that h… | 5 mg | 16608-5 | More Info |
| BIBR 1532 | A mixed-type non-competitive inhibitor of telomerase (IC50 = 93 nM) that h… | 50 mg | 16608-50 | More Info |
| BIBS39 | A nonpeptide AT1 receptor antagonist (Ki = 29 nM in rat lung membranes); s… | 1 mg | 22932-1 | More Info |
| BIBS39 | A nonpeptide AT1 receptor antagonist (Ki = 29 nM in rat lung membranes); s… | 10 mg | 22932-10 | More Info |
| BIBS39 | A nonpeptide AT1 receptor antagonist (Ki = 29 nM in rat lung membranes); s… | 25 mg | 22932-25 | More Info |
| BIBS39 | A nonpeptide AT1 receptor antagonist (Ki = 29 nM in rat lung membranes); s… | 5 mg | 22932-5 | More Info |
| BIBX1382 | An EGFR inhibitor (IC50 = 3 nM); selective for EGFR over HER2 (IC50 = 3,40… | 1 mg | 29630-1 | More Info |
| BIBX1382 | An EGFR inhibitor (IC50 = 3 nM); selective for EGFR over HER2 (IC50 = 3,40… | 10 mg | 29630-10 | More Info |
| BIBX1382 | An EGFR inhibitor (IC50 = 3 nM); selective for EGFR over HER2 (IC50 = 3,40… | 25 mg | 29630-25 | More Info |
| BIBX1382 | An EGFR inhibitor (IC50 = 3 nM); selective for EGFR over HER2 (IC50 = 3,40… | 5 mg | 29630-5 | More Info |
| BI-6C9 | An inhibitor of tBid (Kd = 20 µM), blocking the release of both cyto… | 1 mg | 17265-1 | More Info |
| BI-6C9 | An inhibitor of tBid (Kd = 20 µM), blocking the release of both cyto… | 10 mg | 17265-10 | More Info |
| BI-6C9 | An inhibitor of tBid (Kd = 20 µM), blocking the release of both cyto… | 5 mg | 17265-5 | More Info |
| Bicalutamide | A non-steroidal antiandrogen that binds the androgen receptor (Ki = 12.5 &… | 100 mg | 14250-100 | More Info |
| Bicalutamide | A non-steroidal antiandrogen that binds the androgen receptor (Ki = 12.5 &… | 250 mg | 14250-250 | More Info |
| Bicalutamide | A non-steroidal antiandrogen that binds the androgen receptor (Ki = 12.5 &… | 50 mg | 14250-50 | More Info |
| Bicalutamide | A non-steroidal antiandrogen that binds the androgen receptor (Ki = 12.5 &… | 500 mg | 14250-500 | More Info |
| Bicalutamide-d4 | An internal standard for the quantification of bicalutamide by GC- or LC-M… | 1 mg | 22377-1 | More Info |
| Bicalutamide-d4 | An internal standard for the quantification of bicalutamide by GC- or LC-M… | 500 µg | 22377-500 | More Info |
| Bictegravir | An HIV-1 integrase inhibitor (IC50 = 7.5 nM for strand transfer activity);… | 1 mg | 26532-1 | More Info |
| Bictegravir | An HIV-1 integrase inhibitor (IC50 = 7.5 nM for strand transfer activity);… | 5 mg | 26532-5 | More Info |
| Bictegravir (sodium salt) | An HIV-1 integrase inhibitor (IC50 = 7.5 nM for strand transfer activity);… | 10 mg | 37488-10 | More Info |
| Bictegravir (sodium salt) | An HIV-1 integrase inhibitor (IC50 = 7.5 nM for strand transfer activity);… | 25 mg | 37488-25 | More Info |
| Bictegravir (sodium salt) | An HIV-1 integrase inhibitor (IC50 = 7.5 nM for strand transfer activity);… | 5 mg | 37488-5 | More Info |
| Bictegravir (sodium salt) | An HIV-1 integrase inhibitor (IC50 = 7.5 nM for strand transfer activity);… | 50 mg | 37488-50 | More Info |
| Bicuculline | A competitive GABAA receptor antagonist that at 100 µM blocks sponta… | 100 mg | 11727-100 | More Info |
| Bicuculline | A competitive GABAA receptor antagonist that at 100 µM blocks sponta… | 50 mg | 11727-50 | More Info |
| Bicuculline | A competitive GABAA receptor antagonist that at 100 µM blocks sponta… | 500 mg | 11727-500 | More Info |
| Bicyclol | A hepatoprotective agent; reduces viral DNA and the secretion of HBsAg and… | 1 mg | 21551-1 | More Info |
| Bicyclol | A hepatoprotective agent; reduces viral DNA and the secretion of HBsAg and… | 10 mg | 21551-10 | More Info |
| Bicyclol | A hepatoprotective agent; reduces viral DNA and the secretion of HBsAg and… | 5 mg | 21551-5 | More Info |
| Bicyclomycin Benzoate | An antibiotic produced by S. sapporonensis that inhibits Gram-negative bac… | 25 mg | 15384-25 | More Info |
| Bicyclomycin Benzoate | An antibiotic produced by S. sapporonensis that inhibits Gram-negative bac… | 5 mg | 15384-5 | More Info |
| Bicyclo Prostaglandin E1 | Bicyclo Prostaglandin E1 (bicyclo PGE1) is a stable, base-catalyzed transf… | 1 mg | 13530-1 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
1180 East Ellsworth Road
Ann Arbor MI 48108
P: (734) 971-3335
P: (800) 364-9897 (USA & Canada only)
F: (734) 971-3640
Customer Service: custserv@caymanchem.com
Technical Support: techserv@caymanchem.com
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