CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 693 of 865
Non-Antibody Products
Page 693 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Ractopamine (hydrochloride) | A TAAR1 agonist; increases chloride conductance in X. laevis oocytes expre… | 100 mg | 27613-100 | More Info |
| Ractopamine (hydrochloride) | A TAAR1 agonist; increases chloride conductance in X. laevis oocytes expre… | 250 mg | 27613-250 | More Info |
| Ractopamine (hydrochloride) | A TAAR1 agonist; increases chloride conductance in X. laevis oocytes expre… | 500 mg | 27613-500 | More Info |
| rac-trans-4-hydroxy Glyburide | An active metabolite of glyburide; inhibits glyburide binding to rat brain… | 1 mg | 33752-1 | More Info |
| rac-trans-4-hydroxy Glyburide | An active metabolite of glyburide; inhibits glyburide binding to rat brain… | 5 mg | 33752-5 | More Info |
| rac-trans-4-hydroxy Glyburide | An active metabolite of glyburide; inhibits glyburide binding to rat brain… | 500 µg | 33752-500 | More Info |
| RAD140 | An orally bioavailable SARM that binds to the androgen receptor with a Ki… | 1 mg | 18773-1 | More Info |
| RAD140 | An orally bioavailable SARM that binds to the androgen receptor with a Ki… | 10 mg | 18773-10 | More Info |
| RAD140 | An orally bioavailable SARM that binds to the androgen receptor with a Ki… | 5 mg | 18773-5 | More Info |
| RAD140 | An orally bioavailable SARM that binds to the androgen receptor with a Ki… | 500 µg | 18773-500 | More Info |
| RAD150 | An androgen receptor modulator (IC50 = 130 nM) | 1 mg | 39173-1 | More Info |
| RAD150 | An androgen receptor modulator (IC50 = 130 nM) | 10 mg | 39173-10 | More Info |
| RAD150 | An androgen receptor modulator (IC50 = 130 nM) | 25 mg | 39173-25 | More Info |
| RAD150 | An androgen receptor modulator (IC50 = 130 nM) | 5 mg | 39173-5 | More Info |
| Raddeanin A | A triterpenoid saponin with diverse biological activities; binds to A&beta… | 1 mg | 40235-1 | More Info |
| Raddeanin A | A triterpenoid saponin with diverse biological activities; binds to A&beta… | 10 mg | 40235-10 | More Info |
| Raddeanin A | A triterpenoid saponin with diverse biological activities; binds to A&beta… | 5 mg | 40235-5 | More Info |
| Raddeanin A | A triterpenoid saponin with diverse biological activities; binds to A&beta… | 50 mg | 40235-50 | More Info |
| RAD17-derived Peptide (trifluoroacetate salt) | A peptide substrate for ATR; has been used to identify inhibitors of ATR | 1 mg | 37512-1 | More Info |
| RAD17-derived Peptide (trifluoroacetate salt) | A peptide substrate for ATR; has been used to identify inhibitors of ATR | 10 mg | 37512-10 | More Info |
| RAD17-derived Peptide (trifluoroacetate salt) | A peptide substrate for ATR; has been used to identify inhibitors of ATR | 25 mg | 37512-25 | More Info |
| RAD17-derived Peptide (trifluoroacetate salt) | A peptide substrate for ATR; has been used to identify inhibitors of ATR | 5 mg | 37512-5 | More Info |
| Radezolid | An oxazolidinone antibiotic; active against a variety of bacterial clinica… | 1 mg | 30092-1 | More Info |
| Radezolid | An oxazolidinone antibiotic; active against a variety of bacterial clinica… | 10 mg | 30092-10 | More Info |
| Radezolid | An oxazolidinone antibiotic; active against a variety of bacterial clinica… | 25 mg | 30092-25 | More Info |
| Radezolid | An oxazolidinone antibiotic; active against a variety of bacterial clinica… | 5 mg | 30092-5 | More Info |
| Radicicol | An inhibitor of Hsp90 (IC50 = erb82, and mutant p53; binds to and inhibits… | 1 mg | 13089-1 | More Info |
| Radicicol | An inhibitor of Hsp90 (IC50 = erb82, and mutant p53; binds to and inhibits… | 5 mg | 13089-5 | More Info |
| Radicicol | An inhibitor of Hsp90 (IC50 = erb82, and mutant p53; binds to and inhibits… | 500 µg | 13089-500 | More Info |
| Radicinol | A phytotoxic fungal metabolite | 1 mg | 29861-1 | More Info |
| Radicinol | A phytotoxic fungal metabolite | 5 mg | 29861-5 | More Info |
| RAD51 Inhibitor B02 | A RAD51 inhibitor (IC50 = 27.4 µM in a FRET-based DNA strand exchang… | 10 mg | 22133-10 | More Info |
| RAD51 Inhibitor B02 | A RAD51 inhibitor (IC50 = 27.4 µM in a FRET-based DNA strand exchang… | 25 mg | 22133-25 | More Info |
| RAD51 Inhibitor B02 | A RAD51 inhibitor (IC50 = 27.4 µM in a FRET-based DNA strand exchang… | 5 mg | 22133-5 | More Info |
| RAD51 Inhibitor B02 | A RAD51 inhibitor (IC50 = 27.4 µM in a FRET-based DNA strand exchang… | 50 mg | 22133-50 | More Info |
| Radiprodil | A NR2B subunit-containing NMDA receptor antagonist (IC50 = 8 nM); selectiv… | 10 mg | 29712-10 | More Info |
| Radiprodil | A NR2B subunit-containing NMDA receptor antagonist (IC50 = 8 nM); selectiv… | 25 mg | 29712-25 | More Info |
| Radiprodil | A NR2B subunit-containing NMDA receptor antagonist (IC50 = 8 nM); selectiv… | 5 mg | 29712-5 | More Info |
| Radiprodil | A NR2B subunit-containing NMDA receptor antagonist (IC50 = 8 nM); selectiv… | 50 mg | 29712-50 | More Info |
| Radotinib | A selective second generation Bcr-Abl tyrosine kinase inhibitor (IC50 = 30… | 1 mg | 19923-1 | More Info |
| Radotinib | A selective second generation Bcr-Abl tyrosine kinase inhibitor (IC50 = 30… | 10 mg | 19923-10 | More Info |
| Radotinib | A selective second generation Bcr-Abl tyrosine kinase inhibitor (IC50 = 30… | 25 mg | 19923-25 | More Info |
| Radotinib | A selective second generation Bcr-Abl tyrosine kinase inhibitor (IC50 = 30… | 5 mg | 19923-5 | More Info |
| Radotinib-d6 | An internal standard for the quantification of radotinib by GC- or LC-MS | 1 mg | 30767-1 | More Info |
| RAF265 | A dual inhibitor of mutant B-RafV600E and VEGFR2 (EC50s = 0.14 and 0.19 &m… | 1 mg | 16991-1 | More Info |
| RAF265 | A dual inhibitor of mutant B-RafV600E and VEGFR2 (EC50s = 0.14 and 0.19 &m… | 10 mg | 16991-10 | More Info |
| RAF265 | A dual inhibitor of mutant B-RafV600E and VEGFR2 (EC50s = 0.14 and 0.19 &m… | 5 mg | 16991-5 | More Info |
| RAF265 | A dual inhibitor of mutant B-RafV600E and VEGFR2 (EC50s = 0.14 and 0.19 &m… | 50 mg | 16991-50 | More Info |
| RAF709 | A potent inhibitor of B-RAF and C-RAF (IC50s = 0.4 and 0.5 nM, respectivel… | 1 mg | 23820-1 | More Info |
| RAF709 | A potent inhibitor of B-RAF and C-RAF (IC50s = 0.4 and 0.5 nM, respectivel… | 10 mg | 23820-10 | More Info |
| RAF709 | A potent inhibitor of B-RAF and C-RAF (IC50s = 0.4 and 0.5 nM, respectivel… | 5 mg | 23820-5 | More Info |
| Rafoxanide | An anthelmintic; completely eradicates E. caproni infection in mice at 50… | 1 g | 29616-1 | More Info |
| Rafoxanide | An anthelmintic; completely eradicates E. caproni infection in mice at 50… | 250 mg | 29616-250 | More Info |
| Rafoxanide | An anthelmintic; completely eradicates E. caproni infection in mice at 50… | 500 mg | 29616-500 | More Info |
| 16(R)-AFP 07 (free acid) | An epimer of AFP 07 | 1 mg | 10991-1 | More Info |
| 16(R)-AFP 07 (free acid) | An epimer of AFP 07 | 5 mg | 10991-5 | More Info |
| 16(R)-AFP 07 (free acid) | An epimer of AFP 07 | 500 µg | 10991-500 | More Info |
| RAGE (human, recombinant) | Source: Active recombinant human C-terminal His-tagged RAGE expressed in H… | 1 mg | 38057-1 | More Info |
| RAGE (human, recombinant) | Source: Active recombinant human C-terminal His-tagged RAGE expressed in H… | 100 µg | 38057-100 | More Info |
| Ralinepag | An IP receptor agonist (Ki = 3 nM); selective for IP over DP1 and EP1-4 (K… | 1 mg | 30009-1 | More Info |
| Ralinepag | An IP receptor agonist (Ki = 3 nM); selective for IP over DP1 and EP1-4 (K… | 10 mg | 30009-10 | More Info |
| Ralinepag | An IP receptor agonist (Ki = 3 nM); selective for IP over DP1 and EP1-4 (K… | 25 mg | 30009-25 | More Info |
| Ralinepag | An IP receptor agonist (Ki = 3 nM); selective for IP over DP1 and EP1-4 (K… | 5 mg | 30009-5 | More Info |
| Raloxifene-d4 (hydrochloride) | An internal standard for the quantification of raloxifene by GC- or LC-MS, | 1 mg | 22900-1 | More Info |
| Raloxifene-d4 (hydrochloride) | An internal standard for the quantification of raloxifene by GC- or LC-MS, | 5 mg | 22900-5 | More Info |
| Raloxifene-d4 (hydrochloride) | An internal standard for the quantification of raloxifene by GC- or LC-MS, | 500 µg | 22900-500 | More Info |
| Raloxifene 4'-Glucuronide | A metabolite of raloxifene; binds to the estrogen receptor (IC50 = 370 nM)… | 1 mg | 27831-1 | More Info |
| Raloxifene 6-Glucuronide | A metabolite of raloxifene; formed from raloxifene via UGT1A1 and UGT1A8;… | 1 mg | 27832-1 | More Info |
| Raloxifene (hydrochloride) | A selective estrogen receptor modulator; binds to the estrogen receptor (I… | 100 mg | 10011620-100 | More Info |
| Raloxifene (hydrochloride) | A selective estrogen receptor modulator; binds to the estrogen receptor (I… | 250 mg | 10011620-250 | More Info |
| Raloxifene (hydrochloride) | A selective estrogen receptor modulator; binds to the estrogen receptor (I… | 50 mg | 10011620-50 | More Info |
| Raloxifene (hydrochloride) | A selective estrogen receptor modulator; binds to the estrogen receptor (I… | 500 mg | 10011620-500 | More Info |
| Raloxifene (hydrochloride) | An analytical reference standard categorized as an SERM; has been detected… | 10 mg | 27189-10 | More Info |
| Raloxifene (hydrochloride) | An analytical reference standard categorized as an SERM; has been detected… | 25 mg | 27189-25 | More Info |
| Raloxifene (hydrochloride) | An analytical reference standard categorized as an SERM; has been detected… | 5 mg | 27189-5 | 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
Sales: sales@caymanchem.com
http://www.caymanchem.com
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