CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 734 of 870

Non-Antibody Products
Page 734 of 870
  • Records 54,976 - 55,050 of 65,198
Name Description Size Catalog #
(S)-BAY-598 A selective inhibitor of SMYD2 with IC50 values of 27 nM and in vitro and… 5 mg 18238-5 More Info
(S)-BAY-598 A selective inhibitor of SMYD2 with IC50 values of 27 nM and in vitro and… 500 µg 18238-500 More Info
SB-772077B (hydrochloride) A ROCK inhibitor (IC50s = 5.6 and 6 nM for ROCK1 and ROCK2, respectively);… 1 mg 30975-1 More Info
SB-772077B (hydrochloride) A ROCK inhibitor (IC50s = 5.6 and 6 nM for ROCK1 and ROCK2, respectively);… 5 mg 30975-5 More Info
SBC-110736 A PCSK9 inhibitor; increases LDLR levels in HepG2 cells expressing PCSK9 a… 1 mg 23103-1 More Info
SBC-110736 A PCSK9 inhibitor; increases LDLR levels in HepG2 cells expressing PCSK9 a… 10 mg 23103-10 More Info
SBC-110736 A PCSK9 inhibitor; increases LDLR levels in HepG2 cells expressing PCSK9 a… 25 mg 23103-25 More Info
SBC-110736 A PCSK9 inhibitor; increases LDLR levels in HepG2 cells expressing PCSK9 a… 5 mg 23103-5 More Info
SBC-115076 A modulator of PCSK9 action that blocks LDLR degradation, increasing the u… 1 mg 19134-1 More Info
SBC-115076 A modulator of PCSK9 action that blocks LDLR degradation, increasing the u… 10 mg 19134-10 More Info
SBC-115076 A modulator of PCSK9 action that blocks LDLR degradation, increasing the u… 25 mg 19134-25 More Info
SBC-115076 A modulator of PCSK9 action that blocks LDLR degradation, increasing the u… 5 mg 19134-5 More Info
SB-3CT A selective, mechanism-based inhibitor of MMP-2 and MMP-9 (Kis = 28 and 40… 1 mg 16337-1 More Info
SB-3CT A selective, mechanism-based inhibitor of MMP-2 and MMP-9 (Kis = 28 and 40… 5 mg 16337-5 More Info
SB-3CT A selective, mechanism-based inhibitor of MMP-2 and MMP-9 (Kis = 28 and 40… 500 µg 16337-500 More Info
SBE 13 (hydrochloride) A potent inhibitor of Plk1(IC50 = 0.2 nM) that targets the inactive confor… 10 mg 21241-10 More Info
SBE 13 (hydrochloride) A potent inhibitor of Plk1(IC50 = 0.2 nM) that targets the inactive confor… 25 mg 21241-25 More Info
SBE 13 (hydrochloride) A potent inhibitor of Plk1(IC50 = 0.2 nM) that targets the inactive confor… 5 mg 21241-5 More Info
SBE 13 (hydrochloride) A potent inhibitor of Plk1(IC50 = 0.2 nM) that targets the inactive confor… 50 mg 21241-50 More Info
SBFI AM A membrane-permeant, fluorescent Na+ indicator dye; increasing concentrati… 1 mg 18764-1 More Info
SB-431542 (hydrate) A potent and selective inhibitor of the TGF-β1 receptor ALK5 (IC50 =… 1 mg 13031-1 More Info
SB-431542 (hydrate) A potent and selective inhibitor of the TGF-β1 receptor ALK5 (IC50 =… 10 mg 13031-10 More Info
SB-431542 (hydrate) A potent and selective inhibitor of the TGF-β1 receptor ALK5 (IC50 =… 25 mg 13031-25 More Info
SB-431542 (hydrate) A potent and selective inhibitor of the TGF-β1 receptor ALK5 (IC50 =… 5 mg 13031-5 More Info
SB 202190 (hydrochloride) A potent, selective, and cell-permeable inhibitor of p38 MAP kinases; inhi… 1 mg 21201-1 More Info
SB 202190 (hydrochloride) A potent, selective, and cell-permeable inhibitor of p38 MAP kinases; inhi… 10 mg 21201-10 More Info
SB 202190 (hydrochloride) A potent, selective, and cell-permeable inhibitor of p38 MAP kinases; inhi… 25 mg 21201-25 More Info
SB 202190 (hydrochloride) A potent, selective, and cell-permeable inhibitor of p38 MAP kinases; inhi… 5 mg 21201-5 More Info
SB 203580 (hydrochloride) A formulation with greater solubility in organic solvents than standard SB… 10 mg 13344-10 More Info
SB 203580 (hydrochloride) A formulation with greater solubility in organic solvents than standard SB… 25 mg 13344-25 More Info
SB 203580 (hydrochloride) A formulation with greater solubility in organic solvents than standard SB… 5 mg 13344-5 More Info
SB 203580 (hydrochloride) A formulation with greater solubility in organic solvents than standard SB… 50 mg 13344-50 More Info
SB-200646 (hydrochloride) A dual antagonist of 5-HT2C (Ki = 125 nM in isolated rat cortex) and 5-HT2… 1 mg 30973-1 More Info
SB-200646 (hydrochloride) A dual antagonist of 5-HT2C (Ki = 125 nM in isolated rat cortex) and 5-HT2… 10 mg 30973-10 More Info
SB-200646 (hydrochloride) A dual antagonist of 5-HT2C (Ki = 125 nM in isolated rat cortex) and 5-HT2… 5 mg 30973-5 More Info
SB-206553 (hydrochloride) A 5-HT2C (Ki = 12.6 nM) and 5-HT2B receptor antagonist; selective for 5-HT… 10 mg 34263-10 More Info
SB-206553 (hydrochloride) A 5-HT2C (Ki = 12.6 nM) and 5-HT2B receptor antagonist; selective for 5-HT… 25 mg 34263-25 More Info
SB-206553 (hydrochloride) A 5-HT2C (Ki = 12.6 nM) and 5-HT2B receptor antagonist; selective for 5-HT… 5 mg 34263-5 More Info
SB-206553 (hydrochloride) A 5-HT2C (Ki = 12.6 nM) and 5-HT2B receptor antagonist; selective for 5-HT… 50 mg 34263-50 More Info
SB-216641 (hydrochloride) A 5-HT1B receptor antagonist; binds to 5-HT1B receptors (Ki = 1 nM); selec… 1 mg 32837-1 More Info
SB-216641 (hydrochloride) A 5-HT1B receptor antagonist; binds to 5-HT1B receptors (Ki = 1 nM); selec… 10 mg 32837-10 More Info
SB-216641 (hydrochloride) A 5-HT1B receptor antagonist; binds to 5-HT1B receptors (Ki = 1 nM); selec… 5 mg 32837-5 More Info
SB-224289 (hydrochloride) A potent 5-HT1B inverse agonist (pKi = 8.16) that displays >75-fold select… 10 mg 17036-10 More Info
SB-224289 (hydrochloride) A potent 5-HT1B inverse agonist (pKi = 8.16) that displays >75-fold select… 25 mg 17036-25 More Info
SB-224289 (hydrochloride) A potent 5-HT1B inverse agonist (pKi = 8.16) that displays >75-fold select… 5 mg 17036-5 More Info
SB-224289 (hydrochloride) A potent 5-HT1B inverse agonist (pKi = 8.16) that displays >75-fold select… 50 mg 17036-50 More Info
SB-242084 (hydrochloride) An antagonist of the 5-HT2C receptor (pKi = 9.0), with at least 100-fold m… 1 mg 10096-1 More Info
SB-242084 (hydrochloride) An antagonist of the 5-HT2C receptor (pKi = 9.0), with at least 100-fold m… 10 mg 10096-10 More Info
SB-242084 (hydrochloride) An antagonist of the 5-HT2C receptor (pKi = 9.0), with at least 100-fold m… 5 mg 10096-5 More Info
SB-243213 (hydrochloride) A 5-HT2C receptor inverse agonist; selective for 5-HT2C over the 5-HT2A an… 1 mg 36217-1 More Info
SB-243213 (hydrochloride) A 5-HT2C receptor inverse agonist; selective for 5-HT2C over the 5-HT2A an… 5 mg 36217-5 More Info
SB-258585 (hydrochloride) A potent, selective antagonist of the serotonin 5-HT6 receptor (pKi = 8.53… 1 mg 17416-1 More Info
SB-258585 (hydrochloride) A potent, selective antagonist of the serotonin 5-HT6 receptor (pKi = 8.53… 10 mg 17416-10 More Info
SB-258585 (hydrochloride) A potent, selective antagonist of the serotonin 5-HT6 receptor (pKi = 8.53… 5 mg 17416-5 More Info
SB-258585 (hydrochloride) A potent, selective antagonist of the serotonin 5-HT6 receptor (pKi = 8.53… 50 mg 17416-50 More Info
SB-269970 (hydrochloride) A potent 5-HT7A antagonist (pKi = 8.9) that demonstrates >50-fold binding… 10 mg 17081-10 More Info
SB-269970 (hydrochloride) A potent 5-HT7A antagonist (pKi = 8.9) that demonstrates >50-fold binding… 25 mg 17081-25 More Info
SB-269970 (hydrochloride) A potent 5-HT7A antagonist (pKi = 8.9) that demonstrates >50-fold binding… 5 mg 17081-5 More Info
SB-269970 (hydrochloride) A potent 5-HT7A antagonist (pKi = 8.9) that demonstrates >50-fold binding… 50 mg 17081-50 More Info
SB-271046 (hydrochloride) A selective, orally-available antagonist of the 5-HT6 receptor (pKi = 9.02… 10 mg 18513-10 More Info
SB-271046 (hydrochloride) A selective, orally-available antagonist of the 5-HT6 receptor (pKi = 9.02… 25 mg 18513-25 More Info
SB-271046 (hydrochloride) A selective, orally-available antagonist of the 5-HT6 receptor (pKi = 9.02… 5 mg 18513-5 More Info
SB-271046 (hydrochloride) A selective, orally-available antagonist of the 5-HT6 receptor (pKi = 9.02… 50 mg 18513-50 More Info
SB-399885 (hydrochloride) A 5-HT6 receptor antagonist (Ki = 0.72 nM); >200-fold selective for 5-HT6… 10 mg 32817-10 More Info
SB-399885 (hydrochloride) A 5-HT6 receptor antagonist (Ki = 0.72 nM); >200-fold selective for 5-HT6… 25 mg 32817-25 More Info
SB-399885 (hydrochloride) A 5-HT6 receptor antagonist (Ki = 0.72 nM); >200-fold selective for 5-HT6… 5 mg 32817-5 More Info
SB-399885 (hydrochloride) A 5-HT6 receptor antagonist (Ki = 0.72 nM); >200-fold selective for 5-HT6… 50 mg 32817-50 More Info
SB-743921 (hydrochloride) An Eg5 inhibitor (Ki = 0.5 nM for microtubule-stimulated ATPase activity);… 1 mg 18384-1 More Info
SB-743921 (hydrochloride) An Eg5 inhibitor (Ki = 0.5 nM for microtubule-stimulated ATPase activity);… 10 mg 18384-10 More Info
SB-743921 (hydrochloride) An Eg5 inhibitor (Ki = 0.5 nM for microtubule-stimulated ATPase activity);… 5 mg 18384-5 More Info
SB-743921 (hydrochloride) An Eg5 inhibitor (Ki = 0.5 nM for microtubule-stimulated ATPase activity);… 50 mg 18384-50 More Info
SBI-0206965 An inhibitor of ULK1 (IC50 = 108 nM) that is less effective against ULK2 (… 10 mg 18477-10 More Info
SBI-0206965 An inhibitor of ULK1 (IC50 = 108 nM) that is less effective against ULK2 (… 100 mg 18477-100 More Info
SBI-0206965 An inhibitor of ULK1 (IC50 = 108 nM) that is less effective against ULK2 (… 25 mg 18477-25 More Info
SBI-0206965 An inhibitor of ULK1 (IC50 = 108 nM) that is less effective against ULK2 (… 5 mg 18477-5 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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