CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 770 of 1

Non-Antibody Products
Page 770 of 1,288
  • Records 38,451 - 38,500 of 64,374
Name Description Size Catalog #
ML-336 A quinazolinone-based compound that has been shown to inhibit a VEEV-induc… 5 mg 9001920-5 More Info
ML-345 A selective IDE inhibitor that selectively targets cysteine819 in IDE with… 1 mg 17633-1 More Info
ML-345 A selective IDE inhibitor that selectively targets cysteine819 in IDE with… 10 mg 17633-10 More Info
ML-345 A selective IDE inhibitor that selectively targets cysteine819 in IDE with… 5 mg 17633-5 More Info
ML-346 An activator of the heat shock response; induces the expression of HSP70,… 1 mg 23844-1 More Info
ML-346 An activator of the heat shock response; induces the expression of HSP70,… 10 mg 23844-10 More Info
ML-346 An activator of the heat shock response; induces the expression of HSP70,… 25 mg 23844-25 More Info
ML-346 An activator of the heat shock response; induces the expression of HSP70,… 5 mg 23844-5 More Info
ML-347 Selectively inhibits ALK1 (IC50 = 46 nM) and ALK2 (IC50 = 32 nM) with >300… 1 mg 17640-1 More Info
ML-347 Selectively inhibits ALK1 (IC50 = 46 nM) and ALK2 (IC50 = 32 nM) with >300… 10 mg 17640-10 More Info
ML-347 Selectively inhibits ALK1 (IC50 = 46 nM) and ALK2 (IC50 = 32 nM) with >300… 5 mg 17640-5 More Info
ML-347 Selectively inhibits ALK1 (IC50 = 46 nM) and ALK2 (IC50 = 32 nM) with >300… 50 mg 17640-50 More Info
ML-348 A selective, reversible LYPLA1 inhibitor (IC50 = 210 nM) 1 mg 18523-1 More Info
ML-348 A selective, reversible LYPLA1 inhibitor (IC50 = 210 nM) 10 mg 18523-10 More Info
ML-348 A selective, reversible LYPLA1 inhibitor (IC50 = 210 nM) 25 mg 18523-25 More Info
ML-348 A selective, reversible LYPLA1 inhibitor (IC50 = 210 nM) 5 mg 18523-5 More Info
ML-349 A selective and reversible inhibitor of LYPLA2 (Kis = 230 and >10,000 nM f… 1 mg 20923-1 More Info
ML-349 A selective and reversible inhibitor of LYPLA2 (Kis = 230 and >10,000 nM f… 10 mg 20923-10 More Info
ML-349 A selective and reversible inhibitor of LYPLA2 (Kis = 230 and >10,000 nM f… 5 mg 20923-5 More Info
ML-351 An inhibitor of human reticulocyte 15-LO-1 (IC50 = 200 nM) with >250-fold… 1 mg 16119-1 More Info
ML-351 An inhibitor of human reticulocyte 15-LO-1 (IC50 = 200 nM) with >250-fold… 10 mg 16119-10 More Info
ML-351 An inhibitor of human reticulocyte 15-LO-1 (IC50 = 200 nM) with >250-fold… 25 mg 16119-25 More Info
ML-351 An inhibitor of human reticulocyte 15-LO-1 (IC50 = 200 nM) with >250-fold… 5 mg 16119-5 More Info
ML-352 An inhibitor of the presynaptic choline transporter (Kis = 92 and 166 nM f… 1 mg 21878-1 More Info
ML-352 An inhibitor of the presynaptic choline transporter (Kis = 92 and 166 nM f… 10 mg 21878-10 More Info
ML-352 An inhibitor of the presynaptic choline transporter (Kis = 92 and 166 nM f… 5 mg 21878-5 More Info
ML-354 A PAR4 antagonist (IC50 = 140 nM) that exhibits 71-fold selectivity for PA… 1 mg 19120-1 More Info
ML-354 A PAR4 antagonist (IC50 = 140 nM) that exhibits 71-fold selectivity for PA… 10 mg 19120-10 More Info
ML-354 A PAR4 antagonist (IC50 = 140 nM) that exhibits 71-fold selectivity for PA… 25 mg 19120-25 More Info
ML-354 A PAR4 antagonist (IC50 = 140 nM) that exhibits 71-fold selectivity for PA… 5 mg 19120-5 More Info
ML-355 A selective inhibitor of 12-LO (IC50 = 0.34 µM) with greatly reduced… 1 mg 18537-1 More Info
ML-355 A selective inhibitor of 12-LO (IC50 = 0.34 µM) with greatly reduced… 10 mg 18537-10 More Info
ML-355 A selective inhibitor of 12-LO (IC50 = 0.34 µM) with greatly reduced… 25 mg 18537-25 More Info
ML-355 A selective inhibitor of 12-LO (IC50 = 0.34 µM) with greatly reduced… 5 mg 18537-5 More Info
ML-356 A selective inhibitor of FASN-TE (IC50 = 334 nM); blocks the biosynthesis… 1 mg 20940-1 More Info
ML-356 A selective inhibitor of FASN-TE (IC50 = 334 nM); blocks the biosynthesis… 10 mg 20940-10 More Info
ML-356 A selective inhibitor of FASN-TE (IC50 = 334 nM); blocks the biosynthesis… 5 mg 20940-5 More Info
ML-364 An inhibitor of USP2 (IC50 = 1.1 µM); inhibits the closely related U… 1 mg 21774-1 More Info
ML-364 An inhibitor of USP2 (IC50 = 1.1 µM); inhibits the closely related U… 10 mg 21774-10 More Info
ML-364 An inhibitor of USP2 (IC50 = 1.1 µM); inhibits the closely related U… 25 mg 21774-25 More Info
ML-364 An inhibitor of USP2 (IC50 = 1.1 µM); inhibits the closely related U… 5 mg 21774-5 More Info
ML-365 A TASK-1 potassium channel blocker (IC50 = 16 nM); selective for TASK-1 ov… 1 mg 24666-1 More Info
ML-365 A TASK-1 potassium channel blocker (IC50 = 16 nM); selective for TASK-1 ov… 10 mg 24666-10 More Info
ML-365 A TASK-1 potassium channel blocker (IC50 = 16 nM); selective for TASK-1 ov… 25 mg 24666-25 More Info
ML-365 A TASK-1 potassium channel blocker (IC50 = 16 nM); selective for TASK-1 ov… 5 mg 24666-5 More Info
ML-382 An MRGPRX1 positive allosteric modulator; potentiates BAM 22P (8-22)-induc… 10 mg 36668-10 More Info
ML-382 An MRGPRX1 positive allosteric modulator; potentiates BAM 22P (8-22)-induc… 25 mg 36668-25 More Info
ML-382 An MRGPRX1 positive allosteric modulator; potentiates BAM 22P (8-22)-induc… 5 mg 36668-5 More Info
ML-382 An MRGPRX1 positive allosteric modulator; potentiates BAM 22P (8-22)-induc… 50 mg 36668-50 More Info
ML-385 An inhibitor of Nrf2 (IC50 = 1.9 µM) that blocks downstream target g… 10 mg 21114-10 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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