CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 1 of 1

Non-Antibody Products
Page 1,182 of 1,297
  • Records 59,051 - 59,100 of 64,815
Name Description Size Catalog #
TCS 1102 A dual antagonist of both OX1R and OX2R (Kis = 0.2 and 3 nM, respectively)… 10 mg 18495-10 More Info
TCS 1102 A dual antagonist of both OX1R and OX2R (Kis = 0.2 and 3 nM, respectively)… 25 mg 18495-25 More Info
TCS 1102 A dual antagonist of both OX1R and OX2R (Kis = 0.2 and 3 nM, respectively)… 5 mg 18495-5 More Info
TCS 21311 A JAK3 inhibitor (IC50 = 8 nM); selective for JAK3 over JAK1, JAK2, and TY… 1 mg 30063-1 More Info
TCS 21311 A JAK3 inhibitor (IC50 = 8 nM); selective for JAK3 over JAK1, JAK2, and TY… 10 mg 30063-10 More Info
TCS 21311 A JAK3 inhibitor (IC50 = 8 nM); selective for JAK3 over JAK1, JAK2, and TY… 25 mg 30063-25 More Info
TCS 21311 A JAK3 inhibitor (IC50 = 8 nM); selective for JAK3 over JAK1, JAK2, and TY… 5 mg 30063-5 More Info
TCS 2210 A small molecule inducer of neuronal differentiation; increases expression… 1 mg 16142-1 More Info
TCS 2210 A small molecule inducer of neuronal differentiation; increases expression… 5 mg 16142-5 More Info
TCS 2210 A small molecule inducer of neuronal differentiation; increases expression… 500 µg 16142-500 More Info
TCS 401 A selective inhibitor of PTP1B (Ki = 0.29 µM) 1 mg 20393-1 More Info
TCS 401 A selective inhibitor of PTP1B (Ki = 0.29 µM) 10 mg 20393-10 More Info
TCS 401 A selective inhibitor of PTP1B (Ki = 0.29 µM) 25 mg 20393-25 More Info
TCS 401 A selective inhibitor of PTP1B (Ki = 0.29 µM) 5 mg 20393-5 More Info
TCS 5861528 A selective TRPA1 blocker that antagonizes TRPA1-mediated calcium influx i… 10 mg 18380-10 More Info
TCS 5861528 A selective TRPA1 blocker that antagonizes TRPA1-mediated calcium influx i… 25 mg 18380-25 More Info
TCS 5861528 A selective TRPA1 blocker that antagonizes TRPA1-mediated calcium influx i… 5 mg 18380-5 More Info
TCS 5861528 A selective TRPA1 blocker that antagonizes TRPA1-mediated calcium influx i… 50 mg 18380-50 More Info
TC-S 7001 A ROCK inhibitor (IC50s = 0.6 and 1.1 nM, respectively, for human ROCK1 an… 1 mg 19129-1 More Info
TC-S 7001 A ROCK inhibitor (IC50s = 0.6 and 1.1 nM, respectively, for human ROCK1 an… 5 mg 19129-5 More Info
TC-S 7001 A ROCK inhibitor (IC50s = 0.6 and 1.1 nM, respectively, for human ROCK1 an… 500 µg 19129-500 More Info
TCS ERK 11e A selective inhibitor of ERK2 (Ki 50 = 48 nM) 1 mg 19932-1 More Info
TCS ERK 11e A selective inhibitor of ERK2 (Ki 50 = 48 nM) 10 mg 19932-10 More Info
TCS ERK 11e A selective inhibitor of ERK2 (Ki 50 = 48 nM) 25 mg 19932-25 More Info
TCS ERK 11e A selective inhibitor of ERK2 (Ki 50 = 48 nM) 5 mg 19932-5 More Info
TCS HDAC6 20b An HDAC6 inhibitor; inhibits the growth of HCT116 cells when used at a con… 1 mg 14977-1 More Info
TCS HDAC6 20b An HDAC6 inhibitor; inhibits the growth of HCT116 cells when used at a con… 5 mg 14977-5 More Info
TCS-OX2-29 An antagonist of OX2R (pKi = 7.5) that exhibits >250-fold selectivity for… 10 mg 17419-10 More Info
TCS-OX2-29 An antagonist of OX2R (pKi = 7.5) that exhibits >250-fold selectivity for… 5 mg 17419-5 More Info
TCS-OX2-29 An antagonist of OX2R (pKi = 7.5) that exhibits >250-fold selectivity for… 50 mg 17419-50 More Info
TCS PIM-1 1 An ATP-competitive Pim-1 kinase inhibitor (IC50 = 50 nM) that displays sel… 10 mg 16286-10 More Info
TCS PIM-1 1 An ATP-competitive Pim-1 kinase inhibitor (IC50 = 50 nM) that displays sel… 100 mg 16286-100 More Info
TCS PIM-1 1 An ATP-competitive Pim-1 kinase inhibitor (IC50 = 50 nM) that displays sel… 5 mg 16286-5 More Info
TCS PIM-1 1 An ATP-competitive Pim-1 kinase inhibitor (IC50 = 50 nM) that displays sel… 50 mg 16286-50 More Info
TC 14012 (trifluoroacetate salt) A CXCR4 antagonist (IC50 = 2.9 nM) and CXCR7 agonist; induces β-arres… 1 mg 11974-1 More Info
TC 14012 (trifluoroacetate salt) A CXCR4 antagonist (IC50 = 2.9 nM) and CXCR7 agonist; induces β-arres… 10 mg 11974-10 More Info
TC 14012 (trifluoroacetate salt) A CXCR4 antagonist (IC50 = 2.9 nM) and CXCR7 agonist; induces β-arres… 5 mg 11974-5 More Info
tcY-NH2 (trifluoroacetate salt) A peptide antagonist of PAR4; inhibits platelet aggregation induced by AYP… 1 mg 36758-1 More Info
tcY-NH2 (trifluoroacetate salt) A peptide antagonist of PAR4; inhibits platelet aggregation induced by AYP… 10 mg 36758-10 More Info
tcY-NH2 (trifluoroacetate salt) A peptide antagonist of PAR4; inhibits platelet aggregation induced by AYP… 5 mg 36758-5 More Info
tcY-NH2 (trifluoroacetate salt) A peptide antagonist of PAR4; inhibits platelet aggregation induced by AYP… 500 µg 36758-500 More Info
TD-4208 An antagonist of muscarinic acetylcholine receptors (Kis = 0.42, 0.3, 0.18… 10 mg 36549-10 More Info
TD-4208 An antagonist of muscarinic acetylcholine receptors (Kis = 0.42, 0.3, 0.18… 100 mg 36549-100 More Info
TD-4208 An antagonist of muscarinic acetylcholine receptors (Kis = 0.42, 0.3, 0.18… 25 mg 36549-25 More Info
TD-4208 An antagonist of muscarinic acetylcholine receptors (Kis = 0.42, 0.3, 0.18… 50 mg 36549-50 More Info
TD52 A derivative of erlotinib; decreases the viability of HA22T, Hep3B, PLC /… 10 mg 37744-10 More Info
TD52 A derivative of erlotinib; decreases the viability of HA22T, Hep3B, PLC /… 25 mg 37744-25 More Info
TD52 A derivative of erlotinib; decreases the viability of HA22T, Hep3B, PLC /… 5 mg 37744-5 More Info
TD52 A derivative of erlotinib; decreases the viability of HA22T, Hep3B, PLC /… 50 mg 37744-50 More Info
TDFA (trifluoroacetate salt) A PAD4 inhibitor (IC50 = 2.3 µM); selective for PAD4 over PAD1, PAD2… 1 mg 22484-1 More Info
CAYMAN CHEMICAL COMPANY
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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