CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 3 of 865

Non-Antibody Products
Page 3 of 865
  • Records 151 - 225 of 64,815
Name Description Size Catalog #
A-967079 A potent, selective, and bioavailable inhibitor of the TRPA1 channel, with… 5 mg 15207-5 More Info
A-967079 A potent, selective, and bioavailable inhibitor of the TRPA1 channel, with… 50 mg 15207-50 More Info
A-971432 An S1P5 agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.0… 1 mg 25326-1 More Info
A-971432 An S1P5 agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.0… 10 mg 25326-10 More Info
A-971432 An S1P5 agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.0… 25 mg 25326-25 More Info
A-971432 An S1P5 agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.0… 5 mg 25326-5 More Info
A1-28 An ionizable cationic lipid; has been used in the generation of LNPs for t… 1 mg 39590-1 More Info
A1-28 An ionizable cationic lipid; has been used in the generation of LNPs for t… 5 mg 39590-5 More Info
A1-28 An ionizable cationic lipid; has been used in the generation of LNPs for t… 500 µg 39590-500 More Info
1A-116 An inhibitor of Rac1 (IC50 = 4 µM); reduces the secretion of CXCL5,… 10 mg 40781-10 More Info
1A-116 An inhibitor of Rac1 (IC50 = 4 µM); reduces the secretion of CXCL5,… 100 mg 40781-100 More Info
1A-116 An inhibitor of Rac1 (IC50 = 4 µM); reduces the secretion of CXCL5,… 50 mg 40781-50 More Info
A17 A bile acid derivative; reduces oleic acid-induced triglyceride accumulati… 100 mg 39686-100 More Info
A17 A bile acid derivative; reduces oleic acid-induced triglyceride accumulati… 25 mg 39686-25 More Info
A17 A bile acid derivative; reduces oleic acid-induced triglyceride accumulati… 250 mg 39686-250 More Info
A17 A bile acid derivative; reduces oleic acid-induced triglyceride accumulati… 50 mg 39686-50 More Info
A-39183A An antibiotic; produced by aerobic fermentation of Streptomyces NRRL 12049… 1 mg 23239-1 More Info
A-39183A An antibiotic; produced by aerobic fermentation of Streptomyces NRRL 12049… 5 mg 23239-5 More Info
A-54556A An ADEP antibiotic; active against B. subtilis, S. pyogenes, and E. faecal… 1 mg 15305-1 More Info
A-54556A An ADEP antibiotic; active against B. subtilis, S. pyogenes, and E. faecal… 5 mg 15305-5 More Info
AA147 An ER proteostasis regulator; activates an ATF6-dependent ER stress respon… 10 mg 27143-10 More Info
AA147 An ER proteostasis regulator; activates an ATF6-dependent ER stress respon… 100 mg 27143-100 More Info
AA147 An ER proteostasis regulator; activates an ATF6-dependent ER stress respon… 5 mg 27143-5 More Info
AA147 An ER proteostasis regulator; activates an ATF6-dependent ER stress respon… 50 mg 27143-50 More Info
AA26-8 A pan-serine hydrolase inhibitor; inhibits APEH, PAF-AH2, ABHD11, LYPLA1,… 10 mg 36937-10 More Info
AA26-8 A pan-serine hydrolase inhibitor; inhibits APEH, PAF-AH2, ABHD11, LYPLA1,… 25 mg 36937-25 More Info
AA26-8 A pan-serine hydrolase inhibitor; inhibits APEH, PAF-AH2, ABHD11, LYPLA1,… 5 mg 36937-5 More Info
AA26-8 A pan-serine hydrolase inhibitor; inhibits APEH, PAF-AH2, ABHD11, LYPLA1,… 50 mg 36937-50 More Info
AA-861 A 5-LO inhibitor (IC50 = 0.8 µM); >100-fold selective for 5-LO over… 1 mg 13263-1 More Info
AA-861 A 5-LO inhibitor (IC50 = 0.8 µM); >100-fold selective for 5-LO over… 500 µg 13263-500 More Info
AA92593 An OPN4 receptor antagonist (Ki = 16 nM); inhibits light-induced calcium t… 10 mg 35836-10 More Info
AA92593 An OPN4 receptor antagonist (Ki = 16 nM); inhibits light-induced calcium t… 25 mg 35836-25 More Info
AA92593 An OPN4 receptor antagonist (Ki = 16 nM); inhibits light-induced calcium t… 5 mg 35836-5 More Info
AA92593 An OPN4 receptor antagonist (Ki = 16 nM); inhibits light-induced calcium t… 50 mg 35836-50 More Info
AA43279 An Nav1.1 activator (EC50 = 9.5 µM in a patch-clamp assay using HEK2… 10 mg 40428-10 More Info
AA43279 An Nav1.1 activator (EC50 = 9.5 µM in a patch-clamp assay using HEK2… 25 mg 40428-25 More Info
AA43279 An Nav1.1 activator (EC50 = 9.5 µM in a patch-clamp assay using HEK2… 5 mg 40428-5 More Info
AA43279 An Nav1.1 activator (EC50 = 9.5 µM in a patch-clamp assay using HEK2… 50 mg 40428-50 More Info
AAA A GPR75 antagonist; increases basal GPR75 protein levels and inhibits 20-H… 1 mg 32733-1 More Info
AAA A GPR75 antagonist; increases basal GPR75 protein levels and inhibits 20-H… 500 µg 32733-500 More Info
7-AAD/CFSE Cell-Mediated Cytotoxicity Assay Kit Cayman's 7-AAD / CFSE Cell-Mediated Cytotoxicity Assay Kit employs CFSE to… 1 ea 600120-1EA More Info
AA3-DLin An ionizable cationic amino lipid (pKa = 5.8); has been used in combinatio… 10 mg 37903-10 More Info
AA3-DLin An ionizable cationic amino lipid (pKa = 5.8); has been used in combinatio… 25 mg 37903-25 More Info
AA3-DLin An ionizable cationic amino lipid (pKa = 5.8); has been used in combinatio… 5 mg 37903-5 More Info
AAF-CMK (trifluoroacetate salt) An irreversible inhibitor of TPPII commonly used at 10-100 µM; does… 10 mg 14461-10 More Info
AAF-CMK (trifluoroacetate salt) An irreversible inhibitor of TPPII commonly used at 10-100 µM; does… 25 mg 14461-25 More Info
AAF-CMK (trifluoroacetate salt) An irreversible inhibitor of TPPII commonly used at 10-100 µM; does… 5 mg 14461-5 More Info
17-AAG An inhibitor of Hsp90 (IC50s = 5 and 943 nM for BT474 tumor cell and fibro… 1 mg 11039-1 More Info
17-AAG An inhibitor of Hsp90 (IC50s = 5 and 943 nM for BT474 tumor cell and fibro… 10 mg 11039-10 More Info
17-AAG An inhibitor of Hsp90 (IC50s = 5 and 943 nM for BT474 tumor cell and fibro… 5 mg 11039-5 More Info
AAL-993 A potent inhibitor of VEGF receptors, inhibiting VEGFR1, 2, and 3 with IC5… 1 mg 16351-1 More Info
AAL-993 A potent inhibitor of VEGF receptors, inhibiting VEGFR1, 2, and 3 with IC5… 5 mg 16351-5 More Info
(9,10a)-anti-Δ6a,7-THC An analytical reference standard that is structurally similar to known phy… 1 mg 37046-1 More Info
(9,10a)-anti-Δ6a,7-THC An analytical reference standard that is structurally similar to known phy… 5 mg 37046-5 More Info
AAPH A water-soluble azo compound used extensively as a free radical generator 10 g 82235-10 More Info
AAPH A water-soluble azo compound used extensively as a free radical generator 5 g 82235-5 More Info
A2AR Agonist-1 An agonist of the adenosine A2A receptor and an inhibitor of ENT1 (Kis = 4… 1 mg 28414-1 More Info
A2AR Agonist-1 An agonist of the adenosine A2A receptor and an inhibitor of ENT1 (Kis = 4… 5 mg 28414-5 More Info
A2AR Agonist-1 An agonist of the adenosine A2A receptor and an inhibitor of ENT1 (Kis = 4… 500 µg 28414-500 More Info
AAT-008 An orally bioavailable, potent, and selective EP4 receptor antagonist (IC5… 1 mg 21810-1 More Info
AAT-008 An orally bioavailable, potent, and selective EP4 receptor antagonist (IC5… 10 mg 21810-10 More Info
AAT-008 An orally bioavailable, potent, and selective EP4 receptor antagonist (IC5… 25 mg 21810-25 More Info
AAT-008 An orally bioavailable, potent, and selective EP4 receptor antagonist (IC5… 5 mg 21810-5 More Info
AA-T3A-C12 An ionizable cationic lipidoid; has been used in the generation of LNPs; L… 1 mg 38648-1 More Info
AA-T3A-C12 An ionizable cationic lipidoid; has been used in the generation of LNPs; L… 10 mg 38648-10 More Info
AA-T3A-C12 An ionizable cationic lipidoid; has been used in the generation of LNPs; L… 5 mg 38648-5 More Info
A 26771B A macrolide antibiotic; active against various bacteria (MICs = C. tropica… 1 mg 29593-1 More Info
A-54556B A natural acyldepsipeptide that is effective against Gram-positive bacteri… 2.5 mg 17090-25 More Info
A-54556B A natural acyldepsipeptide that is effective against Gram-positive bacteri… 500 µg 17090-500 More Info
AB-005 A synthetic CB built on a 1-[(1-methylpiperidin-2-yl)methyl]-indole base t… 1 mg 11766-1 More Info
AB-005 A synthetic CB built on a 1-[(1-methylpiperidin-2-yl)methyl]-indole base t… 10 mg 11766-10 More Info
AB-005 A synthetic CB built on a 1-[(1-methylpiperidin-2-yl)methyl]-indole base t… 5 mg 11766-5 More Info
AB-680 An inhibitor of ecto-5'-nucleotidase (IC50 = 0.043 nM in CHO cells express… 1 mg 32798-1 More Info
AB-680 An inhibitor of ecto-5'-nucleotidase (IC50 = 0.043 nM in CHO cells express… 10 mg 32798-10 More Info
AB-680 An inhibitor of ecto-5'-nucleotidase (IC50 = 0.043 nM in CHO cells express… 25 mg 32798-25 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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