CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 94 of 1

Non-Antibody Products
Page 94 of 1,297
  • Records 4,651 - 4,700 of 64,815
Name Description Size Catalog #
Aristolochic Acid C An alkaloid; inhibits the growth of LLC-PK1, P388, HT-29, and HL-60 cancer… 10 mg 28505-10 More Info
Aristolochic Acid C An alkaloid; inhibits the growth of LLC-PK1, P388, HT-29, and HL-60 cancer… 5 mg 28505-5 More Info
Aristolochic Acid D An alkaloid 1 mg 35492-1 More Info
Aristolochic Acid D An alkaloid 10 mg 35492-10 More Info
Aristolochic Acid D An alkaloid 5 mg 35492-5 More Info
Aristolone A sesquiterpene with anticancer activity; cytotoxic to H460, ES-2, and DU1… 10 mg 36157-10 More Info
Aristolone A sesquiterpene with anticancer activity; cytotoxic to H460, ES-2, and DU1… 25 mg 36157-25 More Info
Aristolone A sesquiterpene with anticancer activity; cytotoxic to H460, ES-2, and DU1… 5 mg 36157-5 More Info
Aristolone A sesquiterpene with anticancer activity; cytotoxic to H460, ES-2, and DU1… 50 mg 36157-50 More Info
Arjunolic Acid A triterpene; scavenges DPPH radicals in a cell-free assay at 0.8 mM; prev… 1 mg 29438-1 More Info
Arjunolic Acid A triterpene; scavenges DPPH radicals in a cell-free assay at 0.8 mM; prev… 10 mg 29438-10 More Info
Arjunolic Acid A triterpene; scavenges DPPH radicals in a cell-free assay at 0.8 mM; prev… 5 mg 29438-5 More Info
Arjunolic Acid A triterpene; scavenges DPPH radicals in a cell-free assay at 0.8 mM; prev… 500 µg 29438-500 More Info
ARM1 A thiazolamine that inhibits LTB4 synthesis in human neutrophils (IC50 = ~… 10 mg 15865-10 More Info
ARM1 A thiazolamine that inhibits LTB4 synthesis in human neutrophils (IC50 = ~… 100 mg 15865-100 More Info
ARM1 A thiazolamine that inhibits LTB4 synthesis in human neutrophils (IC50 = ~… 5 mg 15865-5 More Info
ARM1 A thiazolamine that inhibits LTB4 synthesis in human neutrophils (IC50 = ~… 50 mg 15865-50 More Info
ARN1203 A fluorinated analog of AEA that serves as a substrate of FAAH (Km = 29 &m… 1 mg 16065-1 More Info
ARN1203 A fluorinated analog of AEA that serves as a substrate of FAAH (Km = 29 &m… 10 mg 16065-10 More Info
ARN1203 A fluorinated analog of AEA that serves as a substrate of FAAH (Km = 29 &m… 5 mg 16065-5 More Info
ARN1203 A fluorinated analog of AEA that serves as a substrate of FAAH (Km = 29 &m… 500 µg 16065-500 More Info
ARN14686 An affinity probe for NAAA using click chemistry; inhibits the hydrolysis… 1 mg 24261-1 More Info
ARN14686 An affinity probe for NAAA using click chemistry; inhibits the hydrolysis… 10 mg 24261-10 More Info
ARN14686 An affinity probe for NAAA using click chemistry; inhibits the hydrolysis… 25 mg 24261-25 More Info
ARN14686 An affinity probe for NAAA using click chemistry; inhibits the hydrolysis… 5 mg 24261-5 More Info
ARN14974 An inhibitor of acid ceramidase (IC50 = 79 nM); inhibits acid ceramidase a… 1 mg 17119-1 More Info
ARN14974 An inhibitor of acid ceramidase (IC50 = 79 nM); inhibits acid ceramidase a… 10 mg 17119-10 More Info
ARN14974 An inhibitor of acid ceramidase (IC50 = 79 nM); inhibits acid ceramidase a… 25 mg 17119-25 More Info
ARN14974 An inhibitor of acid ceramidase (IC50 = 79 nM); inhibits acid ceramidase a… 5 mg 17119-5 More Info
ARN14988 A potent inhibitor of acid ceramidase (IC50 = 12.8 nM for the human enzyme… 1 mg 24284-1 More Info
ARN14988 A potent inhibitor of acid ceramidase (IC50 = 12.8 nM for the human enzyme… 10 mg 24284-10 More Info
ARN14988 A potent inhibitor of acid ceramidase (IC50 = 12.8 nM for the human enzyme… 25 mg 24284-25 More Info
ARN14988 A potent inhibitor of acid ceramidase (IC50 = 12.8 nM for the human enzyme… 5 mg 24284-5 More Info
ARN19874 An inhibitor of NAPE-PLD (IC50 = 33.7 µM); selective for NAPD-PLD ov… 1 mg 24283-1 More Info
ARN19874 An inhibitor of NAPE-PLD (IC50 = 33.7 µM); selective for NAPD-PLD ov… 10 mg 24283-10 More Info
ARN19874 An inhibitor of NAPE-PLD (IC50 = 33.7 µM); selective for NAPD-PLD ov… 5 mg 24283-5 More Info
ARN19874 An inhibitor of NAPE-PLD (IC50 = 33.7 µM); selective for NAPD-PLD ov… 500 µg 24283-500 More Info
ARN24139 A topoisomerase II poison (IC50 = 7.3 µM); inhibits proliferation of… 1 mg 31062-1 More Info
ARN24139 A topoisomerase II poison (IC50 = 7.3 µM); inhibits proliferation of… 10 mg 31062-10 More Info
ARN24139 A topoisomerase II poison (IC50 = 7.3 µM); inhibits proliferation of… 5 mg 31062-5 More Info
ARN3236 An inhibitor of SIK2 (IC50 = 50s = 21.63 and 6.63 nM, respectively); inhib… 1 mg 31457-1 More Info
ARN3236 An inhibitor of SIK2 (IC50 = 50s = 21.63 and 6.63 nM, respectively); inhib… 10 mg 31457-10 More Info
ARN3236 An inhibitor of SIK2 (IC50 = 50s = 21.63 and 6.63 nM, respectively); inhib… 25 mg 31457-25 More Info
ARN3236 An inhibitor of SIK2 (IC50 = 50s = 21.63 and 6.63 nM, respectively); inhib… 5 mg 31457-5 More Info
ARN-509 An orally bioavailable antagonist of the androgen receptor (IC50 = 16 nM);… 1 mg 17132-1 More Info
ARN-509 An orally bioavailable antagonist of the androgen receptor (IC50 = 16 nM);… 10 mg 17132-10 More Info
ARN-509 An orally bioavailable antagonist of the androgen receptor (IC50 = 16 nM);… 5 mg 17132-5 More Info
ARN726 An NAAA inhibitor (IC50s = 27 and 63 nM for the human and rat enzyme, resp… 1 mg 24259-1 More Info
ARN726 An NAAA inhibitor (IC50s = 27 and 63 nM for the human and rat enzyme, resp… 10 mg 24259-10 More Info
ARN726 An NAAA inhibitor (IC50s = 27 and 63 nM for the human and rat enzyme, resp… 25 mg 24259-25 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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