CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 778 of 870
Non-Antibody Products
Page 778 of 870
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Strontium Ranelate | An antiosteoporotic agent; inhibits 1,25-dihydroxyvitamin D3-induced incre… | 100 mg | 30272-100 | More Info |
| Strontium Ranelate | An antiosteoporotic agent; inhibits 1,25-dihydroxyvitamin D3-induced incre… | 250 mg | 30272-250 | More Info |
| Strontium Ranelate | An antiosteoporotic agent; inhibits 1,25-dihydroxyvitamin D3-induced incre… | 50 mg | 30272-50 | More Info |
| Strophanthidin | A cardenolide with diverse biological activities; inhibits N-acetyltransfe… | 100 mg | 39244-100 | More Info |
| Strophanthidin | A cardenolide with diverse biological activities; inhibits N-acetyltransfe… | 250 mg | 39244-250 | More Info |
| Strophanthidin | A cardenolide with diverse biological activities; inhibits N-acetyltransfe… | 50 mg | 39244-50 | More Info |
| Structure-Based Drug Design | Our structure-based drug design (SBDD) services are supported by medicinal… | n/a | n/a | More Info |
| Structure Determination | Our structural biology experts, with proven experience in biophysical char… | n/a | n/a | More Info |
| Strychnospermine | An alkaloid | 1 mg | 29988-1 | More Info |
| Strychnospermine | An alkaloid | 5 mg | 29988-5 | More Info |
| STX140 | An estrogen sulfamate with anticancer activities; inhibits steroid sulfata… | 1 mg | 27863-1 | More Info |
| STX140 | An estrogen sulfamate with anticancer activities; inhibits steroid sulfata… | 10 mg | 27863-10 | More Info |
| STX140 | An estrogen sulfamate with anticancer activities; inhibits steroid sulfata… | 5 mg | 27863-5 | More Info |
| STX-64 | A steroid sulfatase inhibitor (IC50 = 0.008 µM in placental microsom… | 1 mg | 9003206-1 | More Info |
| STX-64 | A steroid sulfatase inhibitor (IC50 = 0.008 µM in placental microsom… | 10 mg | 9003206-10 | More Info |
| STX-64 | A steroid sulfatase inhibitor (IC50 = 0.008 µM in placental microsom… | 25 mg | 9003206-25 | More Info |
| STX-64 | A steroid sulfatase inhibitor (IC50 = 0.008 µM in placental microsom… | 5 mg | 9003206-5 | More Info |
| STY-BODIPY | A fluorogenic probe for radical-trapping antioxidant activity; co-autoxida… | 1 mg | 27089-1 | More Info |
| STY-BODIPY | A fluorogenic probe for radical-trapping antioxidant activity; co-autoxida… | 5 mg | 27089-5 | More Info |
| STY-BODIPY | A fluorogenic probe for radical-trapping antioxidant activity; co-autoxida… | 500 µg | 27089-500 | More Info |
| SU 0268 | An OGG1 inhibitor (IC50 = 0.059 µM); selective for OGG1 over the DNA… | 1 mg | 36064-1 | More Info |
| SU 0268 | An OGG1 inhibitor (IC50 = 0.059 µM); selective for OGG1 over the DNA… | 10 mg | 36064-10 | More Info |
| SU 0268 | An OGG1 inhibitor (IC50 = 0.059 µM); selective for OGG1 over the DNA… | 25 mg | 36064-25 | More Info |
| SU 0268 | An OGG1 inhibitor (IC50 = 0.059 µM); selective for OGG1 over the DNA… | 5 mg | 36064-5 | More Info |
| SU 14813 | A dual VEGFR and PDGFR family kinase inhibitor (IC50s = 0.002, 0.05, 0.004… | 100 mg | 31514-100 | More Info |
| SU 14813 | A dual VEGFR and PDGFR family kinase inhibitor (IC50s = 0.002, 0.05, 0.004… | 25 mg | 31514-25 | More Info |
| SU 14813 | A dual VEGFR and PDGFR family kinase inhibitor (IC50s = 0.002, 0.05, 0.004… | 5 mg | 31514-5 | More Info |
| SU 14813 | A dual VEGFR and PDGFR family kinase inhibitor (IC50s = 0.002, 0.05, 0.004… | 50 mg | 31514-50 | More Info |
| SU 1498 | A selective inhibitor of VEGFR2 (aka FLK1; IC50 = 700 nM), having negligib… | 1 mg | 16354-1 | More Info |
| SU 1498 | A selective inhibitor of VEGFR2 (aka FLK1; IC50 = 700 nM), having negligib… | 5 mg | 16354-5 | More Info |
| SU 1498 | A selective inhibitor of VEGFR2 (aka FLK1; IC50 = 700 nM), having negligib… | 500 µg | 16354-500 | More Info |
| SU 4312 | A selective inhibitor of VEGFR2 and PDGFR tyrosine kinases (IC50s = 0.8 an… | 1 mg | 20213-1 | More Info |
| SU 4312 | A selective inhibitor of VEGFR2 and PDGFR tyrosine kinases (IC50s = 0.8 an… | 10 mg | 20213-10 | More Info |
| SU 4312 | A selective inhibitor of VEGFR2 and PDGFR tyrosine kinases (IC50s = 0.8 an… | 25 mg | 20213-25 | More Info |
| SU 4312 | A selective inhibitor of VEGFR2 and PDGFR tyrosine kinases (IC50s = 0.8 an… | 5 mg | 20213-5 | More Info |
| SU 4942 | A modulator of tyrosine kinase signaling; inhibits VEGF- or acidic FGF-ind… | 100 mg | 32967-100 | More Info |
| SU 4942 | A modulator of tyrosine kinase signaling; inhibits VEGF- or acidic FGF-ind… | 250 mg | 32967-250 | More Info |
| SU 4942 | A modulator of tyrosine kinase signaling; inhibits VEGF- or acidic FGF-ind… | 50 mg | 32967-50 | More Info |
| SU 4942 | A modulator of tyrosine kinase signaling; inhibits VEGF- or acidic FGF-ind… | 500 mg | 32967-500 | More Info |
| SU 5201 | An inhibitor of IL-2 production (IC50 = 1 nM in PBMCs); inhibits VEGF- or… | 1 g | 34333-1 | More Info |
| SU 5201 | An inhibitor of IL-2 production (IC50 = 1 nM in PBMCs); inhibits VEGF- or… | 100 mg | 34333-100 | More Info |
| SU 5201 | An inhibitor of IL-2 production (IC50 = 1 nM in PBMCs); inhibits VEGF- or… | 50 mg | 34333-50 | More Info |
| SU 5201 | An inhibitor of IL-2 production (IC50 = 1 nM in PBMCs); inhibits VEGF- or… | 500 mg | 34333-500 | More Info |
| SU 5205 | An inhibitor of VEGFR2 / FLK1 (IC50 = 9.6 µM); inhibits HUVEC mitoge… | 100 mg | 27310-100 | More Info |
| SU 5205 | An inhibitor of VEGFR2 / FLK1 (IC50 = 9.6 µM); inhibits HUVEC mitoge… | 250 mg | 27310-250 | More Info |
| SU 5205 | An inhibitor of VEGFR2 / FLK1 (IC50 = 9.6 µM); inhibits HUVEC mitoge… | 50 mg | 27310-50 | More Info |
| SU 5214 | A 3-heteroaryl-2-indoline; designed in a drug discovery program for develo… | 25 mg | 24670-25 | More Info |
| SU 5214 | A 3-heteroaryl-2-indoline; designed in a drug discovery program for develo… | 5 mg | 24670-5 | More Info |
| SU 5214 | A 3-heteroaryl-2-indoline; designed in a drug discovery program for develo… | 50 mg | 24670-50 | More Info |
| SU 5402 | An inhibitor of the tyrosine kinase domains of VEGFR2, FGFR1, and PDGFR&be… | 1 mg | 13182-1 | More Info |
| SU 5402 | An inhibitor of the tyrosine kinase domains of VEGFR2, FGFR1, and PDGFR&be… | 10 mg | 13182-10 | More Info |
| SU 5402 | An inhibitor of the tyrosine kinase domains of VEGFR2, FGFR1, and PDGFR&be… | 25 mg | 13182-25 | More Info |
| SU 5402 | An inhibitor of the tyrosine kinase domains of VEGFR2, FGFR1, and PDGFR&be… | 5 mg | 13182-5 | More Info |
| SU 5416 | A tyrosine kinase inhibitor best known as an inhibitor of VEGFR2 (FLK1 / K… | 10 mg | 13342-10 | More Info |
| SU 5416 | A tyrosine kinase inhibitor best known as an inhibitor of VEGFR2 (FLK1 / K… | 100 mg | 13342-100 | More Info |
| SU 5416 | A tyrosine kinase inhibitor best known as an inhibitor of VEGFR2 (FLK1 / K… | 25 mg | 13342-25 | More Info |
| SU 5416 | A tyrosine kinase inhibitor best known as an inhibitor of VEGFR2 (FLK1 / K… | 50 mg | 13342-50 | More Info |
| SU 5614 | A multi-kinase inhibitor; inhibits growth and induces apoptosis in Ba / F3… | 1 mg | 17410-1 | More Info |
| SU 5614 | A multi-kinase inhibitor; inhibits growth and induces apoptosis in Ba / F3… | 10 mg | 17410-10 | More Info |
| SU 5614 | A multi-kinase inhibitor; inhibits growth and induces apoptosis in Ba / F3… | 25 mg | 17410-25 | More Info |
| SU 5614 | A multi-kinase inhibitor; inhibits growth and induces apoptosis in Ba / F3… | 5 mg | 17410-5 | More Info |
| SU 6668 | An inhibitor of PDGFRβ, VEGFR2, and FGFR1 (IC50 = 0.06, 2.4, and 3.0… | 1 mg | 13873-1 | More Info |
| SU 6668 | An inhibitor of PDGFRβ, VEGFR2, and FGFR1 (IC50 = 0.06, 2.4, and 3.0… | 10 mg | 13873-10 | More Info |
| SU 6668 | An inhibitor of PDGFRβ, VEGFR2, and FGFR1 (IC50 = 0.06, 2.4, and 3.0… | 5 mg | 13873-5 | More Info |
| SU 9516 | A potent inhibitor of several CDKs with selectivity for Cdk2 (IC50s = 22,… | 1 mg | 14796-1 | More Info |
| SU 9516 | A potent inhibitor of several CDKs with selectivity for Cdk2 (IC50s = 22,… | 10 mg | 14796-10 | More Info |
| SU 9516 | A potent inhibitor of several CDKs with selectivity for Cdk2 (IC50s = 22,… | 25 mg | 14796-25 | More Info |
| SU 9516 | A potent inhibitor of several CDKs with selectivity for Cdk2 (IC50s = 22,… | 5 mg | 14796-5 | More Info |
| SU11274 | A potent, selective, ATP-competitive inhibitor of c-Met (IC50 = 20 nM); in… | 1 mg | 14861-1 | More Info |
| SU11274 | A potent, selective, ATP-competitive inhibitor of c-Met (IC50 = 20 nM); in… | 5 mg | 14861-5 | More Info |
| SU11274 | A potent, selective, ATP-competitive inhibitor of c-Met (IC50 = 20 nM); in… | 500 µg | 14861-500 | More Info |
| SU6656 | A selective inhibitor of Src kinases, including Src, Yes, Lyn, and Fyn (IC… | 1 mg | 13338-1 | More Info |
| SU6656 | A selective inhibitor of Src kinases, including Src, Yes, Lyn, and Fyn (IC… | 10 mg | 13338-10 | More Info |
| SU6656 | A selective inhibitor of Src kinases, including Src, Yes, Lyn, and Fyn (IC… | 25 mg | 13338-25 | More Info |
| SU6656 | A selective inhibitor of Src kinases, including Src, Yes, Lyn, and Fyn (IC… | 5 mg | 13338-5 | 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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