CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 188 of 1

Non-Antibody Products
Page 188 of 1,297
  • Records 9,351 - 9,400 of 64,815
Name Description Size Catalog #
BZO-POXIZID An analytical reference standard categorized as a synthetic cannabinoid; i… 5 mg 34795-5 More Info
BZO-POXIZID-d9 An internal standard for the quantification of BZO-POXIZID by GC- or LC-MS… 1 mg 36799-1 More Info
2-BZP An analytical reference standard categorized as a piperazine; intended for… 1 mg 24419-1 More Info
2-BZP An analytical reference standard categorized as a piperazine; intended for… 5 mg 24419-5 More Info
Bz-RS-ISer(3-Ph)-OMe An intermediate in the synthesis of 7-epi-10-deacetyltaxol 1 g 40291-1 More Info
Bz-RS-ISer(3-Ph)-OMe An intermediate in the synthesis of 7-epi-10-deacetyltaxol 10 g 40291-10 More Info
Bz-RS-ISer(3-Ph)-OMe An intermediate in the synthesis of 7-epi-10-deacetyltaxol 5 g 40291-5 More Info
246C10 An ionizable cationic lipid (pKa = 6.75); has been used in combination wit… 10 mg 37907-10 More Info
246C10 An ionizable cationic lipid (pKa = 6.75); has been used in combination wit… 25 mg 37907-25 More Info
246C10 An ionizable cationic lipid (pKa = 6.75); has been used in combination wit… 5 mg 37907-5 More Info
680C91 A TDO inhibitor (IC50s = 1.46 and 0.28 µM for the mouse and human en… 10 mg 34823-10 More Info
680C91 A TDO inhibitor (IC50s = 1.46 and 0.28 µM for the mouse and human en… 25 mg 34823-25 More Info
680C91 A TDO inhibitor (IC50s = 1.46 and 0.28 µM for the mouse and human en… 5 mg 34823-5 More Info
680C91 A TDO inhibitor (IC50s = 1.46 and 0.28 µM for the mouse and human en… 50 mg 34823-50 More Info
C-02 A PROTAC that drives hexokinase 2 degradation; induces degradation of hexo… 1 mg 39384-1 More Info
C-02 A PROTAC that drives hexokinase 2 degradation; induces degradation of hexo… 5 mg 39384-5 More Info
C-02 A PROTAC that drives hexokinase 2 degradation; induces degradation of hexo… 500 µg 39384-500 More Info
C12-113 An ionizable cationic lipidoid; has been used in combination with other li… 10 mg 39335-10 More Info
C12-113 An ionizable cationic lipidoid; has been used in combination with other li… 25 mg 39335-25 More Info
C12-113 An ionizable cationic lipidoid; has been used in combination with other li… 5 mg 39335-5 More Info
C12-200 A branched-chain ionizable cationic lipidoid; has been used in combination… 10 mg 36699-10 More Info
C12-200 A branched-chain ionizable cationic lipidoid; has been used in combination… 100 mg 36699-100 More Info
C12-200 A branched-chain ionizable cationic lipidoid; has been used in combination… 25 mg 36699-25 More Info
C12-200 A branched-chain ionizable cationic lipidoid; has been used in combination… 50 mg 36699-50 More Info
C14-4 An ionizable cationic lipid; has been used in the generation of lipid nano… 1 mg 38942-1 More Info
C14-4 An ionizable cationic lipid; has been used in the generation of lipid nano… 10 mg 38942-10 More Info
C14-4 An ionizable cationic lipid; has been used in the generation of lipid nano… 5 mg 38942-5 More Info
C-170 A STING inhibitor; binds to STING, inhibits its palmitoylation, and preven… 10 mg 30157-10 More Info
C-170 A STING inhibitor; binds to STING, inhibits its palmitoylation, and preven… 100 mg 30157-100 More Info
C-170 A STING inhibitor; binds to STING, inhibits its palmitoylation, and preven… 25 mg 30157-25 More Info
C-170 A STING inhibitor; binds to STING, inhibits its palmitoylation, and preven… 50 mg 30157-50 More Info
C-171 A STING inhibitor; binds to STING, inhibits its palmitoylation, and preven… 10 mg 30159-10 More Info
C-171 A STING inhibitor; binds to STING, inhibits its palmitoylation, and preven… 100 mg 30159-100 More Info
C-171 A STING inhibitor; binds to STING, inhibits its palmitoylation, and preven… 25 mg 30159-25 More Info
C-171 A STING inhibitor; binds to STING, inhibits its palmitoylation, and preven… 50 mg 30159-50 More Info
C-176 A STING inhibitor; reduces STING-, but not RIG-I or TBK1-, mediated IFN-&b… 10 mg 25859-10 More Info
C-176 A STING inhibitor; reduces STING-, but not RIG-I or TBK1-, mediated IFN-&b… 100 mg 25859-100 More Info
C-176 A STING inhibitor; reduces STING-, but not RIG-I or TBK1-, mediated IFN-&b… 25 mg 25859-25 More Info
C-176 A STING inhibitor; reduces STING-, but not RIG-I or TBK1-, mediated IFN-&b… 50 mg 25859-50 More Info
C-178 A STING inhibitor; binds to Cys91 on STING to block its and prevents recru… 10 mg 25860-10 More Info
C-178 A STING inhibitor; binds to Cys91 on STING to block its and prevents recru… 25 mg 25860-25 More Info
C-178 A STING inhibitor; binds to Cys91 on STING to block its and prevents recru… 5 mg 25860-5 More Info
C-178 A STING inhibitor; binds to Cys91 on STING to block its and prevents recru… 50 mg 25860-50 More Info
C18 A covalent GPX4 inhibitor (IC50 = 120 nM); inhibits the growth of MDA-MB-4… 1 mg 39432-1 More Info
C18 A covalent GPX4 inhibitor (IC50 = 120 nM); inhibits the growth of MDA-MB-4… 10 mg 39432-10 More Info
C18 A covalent GPX4 inhibitor (IC50 = 120 nM); inhibits the growth of MDA-MB-4… 25 mg 39432-25 More Info
C18 A covalent GPX4 inhibitor (IC50 = 120 nM); inhibits the growth of MDA-MB-4… 5 mg 39432-5 More Info
C188-9 A STAT3 inhibitor; binds to the STAT3 SH2 domain (Ki = 136 nM) and inhibit… 10 mg 30928-10 More Info
C188-9 A STAT3 inhibitor; binds to the STAT3 SH2 domain (Ki = 136 nM) and inhibit… 25 mg 30928-25 More Info
C188-9 A STAT3 inhibitor; binds to the STAT3 SH2 domain (Ki = 136 nM) and inhibit… 5 mg 30928-5 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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