CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 195 of 859
Non-Antibody Products
Page 195 of 859
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| CTP354 | A deuterated derivative of L-838,417; binds to the GABAA receptor benzodia… | 10 mg | 36618-10 | More Info |
| CTP354 | A deuterated derivative of L-838,417; binds to the GABAA receptor benzodia… | 25 mg | 36618-25 | More Info |
| CTP354 | A deuterated derivative of L-838,417; binds to the GABAA receptor benzodia… | 5 mg | 36618-5 | More Info |
| CTP354 | A deuterated derivative of L-838,417; binds to the GABAA receptor benzodia… | 50 mg | 36618-50 | More Info |
| CTPB | An amide derivative that selectively activates the HAT p300, with maximal… | 1 mg | 19570-1 | More Info |
| CTPB | An amide derivative that selectively activates the HAT p300, with maximal… | 5 mg | 19570-5 | More Info |
| CTPI-2 | A mitochondrial citrate transporter inhibitor; decreases the OCR in tumor… | 100 mg | 36933-100 | More Info |
| CTPI-2 | A mitochondrial citrate transporter inhibitor; decreases the OCR in tumor… | 250 mg | 36933-250 | More Info |
| CTPI-2 | A mitochondrial citrate transporter inhibitor; decreases the OCR in tumor… | 50 mg | 36933-50 | More Info |
| CTPI-2 | A mitochondrial citrate transporter inhibitor; decreases the OCR in tumor… | 500 mg | 36933-500 | More Info |
| C13-112-tri-tail | An ionizable cationic lipid | 1 mg | 38383-1 | More Info |
| C13-112-tri-tail | An ionizable cationic lipid | 10 mg | 38383-10 | More Info |
| C13-112-tri-tail | An ionizable cationic lipid | 25 mg | 38383-25 | More Info |
| C13-112-tri-tail | An ionizable cationic lipid | 5 mg | 38383-5 | More Info |
| CTS-1027 | An inhibitor of MMPs; selective for MMP-2, MMP-9, and MMP-13 (Kis= 0.22, 0… | 1 mg | 33219-1 | More Info |
| CTS-1027 | An inhibitor of MMPs; selective for MMP-2, MMP-9, and MMP-13 (Kis= 0.22, 0… | 5 mg | 33219-5 | More Info |
| CTS-1027 | An inhibitor of MMPs; selective for MMP-2, MMP-9, and MMP-13 (Kis= 0.22, 0… | 500 µg | 33219-500 | More Info |
| CTX-0294885 | A broad spectrum kinase inhibitor used in proteomics; inhibits FAK, Flt3,… | 1 mg | 22197-1 | More Info |
| CTX-0294885 | A broad spectrum kinase inhibitor used in proteomics; inhibits FAK, Flt3,… | 10 mg | 22197-10 | More Info |
| CTX-0294885 | A broad spectrum kinase inhibitor used in proteomics; inhibits FAK, Flt3,… | 25 mg | 22197-25 | More Info |
| CTX-0294885 | A broad spectrum kinase inhibitor used in proteomics; inhibits FAK, Flt3,… | 5 mg | 22197-5 | More Info |
| C-Type Natriuretic Peptide-22 (human, porcine, rat) (trifluoroacetate salt) | An endogenous peptide with diverse biological activities; a selective agon… | 1 mg | 24401-1 | More Info |
| C-Type Natriuretic Peptide-22 (human, porcine, rat) (trifluoroacetate salt) | An endogenous peptide with diverse biological activities; a selective agon… | 500 µg | 24401-500 | More Info |
| CU-115 | A TLR8 antagonist (IC50 = 1.04 µM); selective for TLR8 over TLR7 (IC… | 1 mg | 29815-1 | More Info |
| CU-115 | A TLR8 antagonist (IC50 = 1.04 µM); selective for TLR8 over TLR7 (IC… | 10 mg | 29815-10 | More Info |
| CU-115 | A TLR8 antagonist (IC50 = 1.04 µM); selective for TLR8 over TLR7 (IC… | 5 mg | 29815-5 | More Info |
| CU-32 | A cGAS inhibitor (IC50 = 0.45 µM); reduces DNA-, but not Sendai viru… | 1 mg | 31029-1 | More Info |
| CU-32 | A cGAS inhibitor (IC50 = 0.45 µM); reduces DNA-, but not Sendai viru… | 10 mg | 31029-10 | More Info |
| CU-32 | A cGAS inhibitor (IC50 = 0.45 µM); reduces DNA-, but not Sendai viru… | 5 mg | 31029-5 | More Info |
| CU-76 | A cGAS inhibitor (IC50 = 0.24 µM); reduces DNA-induced dimerization… | 1 mg | 31030-1 | More Info |
| CU-76 | A cGAS inhibitor (IC50 = 0.24 µM); reduces DNA-induced dimerization… | 10 mg | 31030-10 | More Info |
| CU-76 | A cGAS inhibitor (IC50 = 0.24 µM); reduces DNA-induced dimerization… | 5 mg | 31030-5 | More Info |
| Cu-ATSM | A copper-containing compound with diverse biological activities; inhibits… | 1 mg | 17122-1 | More Info |
| Cu-ATSM | A copper-containing compound with diverse biological activities; inhibits… | 10 mg | 17122-10 | More Info |
| Cu-ATSM | A copper-containing compound with diverse biological activities; inhibits… | 25 mg | 17122-25 | More Info |
| Cu-ATSM | A copper-containing compound with diverse biological activities; inhibits… | 5 mg | 17122-5 | More Info |
| Cu-ATSP | A copper-containing bis(thiosemicarbazone) complex; traps peroxyl radicals… | 1 mg | 35322-1 | More Info |
| Cu-ATSP | A copper-containing bis(thiosemicarbazone) complex; traps peroxyl radicals… | 10 mg | 35322-10 | More Info |
| Cu-ATSP | A copper-containing bis(thiosemicarbazone) complex; traps peroxyl radicals… | 25 mg | 35322-25 | More Info |
| Cu-ATSP | A copper-containing bis(thiosemicarbazone) complex; traps peroxyl radicals… | 5 mg | 35322-5 | More Info |
| CU CPT 22 | An antagonist of TLR1 / TLR2 (Ki = 0.41 µM); inhibits Pam3CSK4-induc… | 1 mg | 15244-1 | More Info |
| CU CPT 22 | An antagonist of TLR1 / TLR2 (Ki = 0.41 µM); inhibits Pam3CSK4-induc… | 10 mg | 15244-10 | More Info |
| CU CPT 22 | An antagonist of TLR1 / TLR2 (Ki = 0.41 µM); inhibits Pam3CSK4-induc… | 5 mg | 15244-5 | More Info |
| CU-CPT4a | A TLR3 antagonist (IC50 = 3.44 µM); selective for TLR3 over TLR4, TL… | 1 mg | 30951-1 | More Info |
| CU-CPT4a | A TLR3 antagonist (IC50 = 3.44 µM); selective for TLR3 over TLR4, TL… | 5 mg | 30951-5 | More Info |
| CU-CPT4a | A TLR3 antagonist (IC50 = 3.44 µM); selective for TLR3 over TLR4, TL… | 500 µg | 30951-500 | More Info |
| CU-CPT9a | A TLR8 antagonist; inhibits R-848-induced activation of NF-κB in TLR… | 1 mg | 28722-1 | More Info |
| CU-CPT9a | A TLR8 antagonist; inhibits R-848-induced activation of NF-κB in TLR… | 10 mg | 28722-10 | More Info |
| CU-CPT9a | A TLR8 antagonist; inhibits R-848-induced activation of NF-κB in TLR… | 25 mg | 28722-25 | More Info |
| CU-CPT9a | A TLR8 antagonist; inhibits R-848-induced activation of NF-κB in TLR… | 5 mg | 28722-5 | More Info |
| CU-CPT9b | A TLR8 antagonist; inhibits R-848-induced activation of NF-κB in TLR… | 1 mg | 28723-1 | More Info |
| CU-CPT9b | A TLR8 antagonist; inhibits R-848-induced activation of NF-κB in TLR… | 10 mg | 28723-10 | More Info |
| CU-CPT9b | A TLR8 antagonist; inhibits R-848-induced activation of NF-κB in TLR… | 25 mg | 28723-25 | More Info |
| CU-CPT9b | A TLR8 antagonist; inhibits R-848-induced activation of NF-κB in TLR… | 5 mg | 28723-5 | More Info |
| CU-CPT17e | A TLR3, TLR8, and TLR9 receptor agonist; selectively induces NF-κB a… | 1 mg | 39534-1 | More Info |
| CU-CPT17e | A TLR3, TLR8, and TLR9 receptor agonist; selectively induces NF-κB a… | 10 mg | 39534-10 | More Info |
| CU-CPT17e | A TLR3, TLR8, and TLR9 receptor agonist; selectively induces NF-κB a… | 25 mg | 39534-25 | More Info |
| CU-CPT17e | A TLR3, TLR8, and TLR9 receptor agonist; selectively induces NF-κB a… | 5 mg | 39534-5 | More Info |
| CU-CPT8m | An antagonist of TLR8 (Kd = 220 nM; IC50 = 67 nM in a reporter assay); is… | 1 mg | 25349-1 | More Info |
| CU-CPT8m | An antagonist of TLR8 (Kd = 220 nM; IC50 = 67 nM in a reporter assay); is… | 10 mg | 25349-10 | More Info |
| CU-CPT8m | An antagonist of TLR8 (Kd = 220 nM; IC50 = 67 nM in a reporter assay); is… | 25 mg | 25349-25 | More Info |
| CU-CPT8m | An antagonist of TLR8 (Kd = 220 nM; IC50 = 67 nM in a reporter assay); is… | 5 mg | 25349-5 | More Info |
| Cucurbitacin B | A plant-derived steroidal triterpene that induces cell cycle arrest or apo… | 1 mg | 14820-1 | More Info |
| Cucurbitacin B | A plant-derived steroidal triterpene that induces cell cycle arrest or apo… | 10 mg | 14820-10 | More Info |
| Cucurbitacin B | A plant-derived steroidal triterpene that induces cell cycle arrest or apo… | 25 mg | 14820-25 | More Info |
| Cucurbitacin B | A plant-derived steroidal triterpene that induces cell cycle arrest or apo… | 5 mg | 14820-5 | More Info |
| Cucurbitacin D | A triterpenoid; decreases levels of HER2, Raf, and Cdk6 in MCF-7 cell lysa… | 1 mg | 36172-1 | More Info |
| Cucurbitacin D | A triterpenoid; decreases levels of HER2, Raf, and Cdk6 in MCF-7 cell lysa… | 10 mg | 36172-10 | More Info |
| Cucurbitacin D | A triterpenoid; decreases levels of HER2, Raf, and Cdk6 in MCF-7 cell lysa… | 5 mg | 36172-5 | More Info |
| Cucurbitacin E | A natural triterpene; reduces MPP+-induced death of neuronal PC12 cells th… | 1 mg | 14821-1 | More Info |
| Cucurbitacin E | A natural triterpene; reduces MPP+-induced death of neuronal PC12 cells th… | 10 mg | 14821-10 | More Info |
| Cucurbitacin E | A natural triterpene; reduces MPP+-induced death of neuronal PC12 cells th… | 25 mg | 14821-25 | More Info |
| Cucurbitacin E | A natural triterpene; reduces MPP+-induced death of neuronal PC12 cells th… | 5 mg | 14821-5 | More Info |
| Cucurbitacin I | A potent inhibitor of the STAT3 / JAK signaling pathway; suppresses levels… | 1 mg | 14747-1 | More Info |
| Cucurbitacin I | A potent inhibitor of the STAT3 / JAK signaling pathway; suppresses levels… | 10 mg | 14747-10 | More Info |
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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