CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 196 of 865
Non-Antibody Products
Page 196 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| CTEP | An inverse agonist of mGluR5 (Kis = 16.4, 12.6, and 9.5 nM for the human,… | 50 mg | 28773-50 | More Info |
| C13-112-tetra-tail | An ionizable cationic lipid | 1 mg | 38329-1 | More Info |
| C13-112-tetra-tail | An ionizable cationic lipid | 10 mg | 38329-10 | More Info |
| C13-112-tetra-tail | An ionizable cationic lipid | 5 mg | 38329-5 | More Info |
| 2C-TFM (hydrochloride) | A 2C compound with a para-trifluoromethyl substitution. It is a potent ago… | 1 mg | 14471-1 | More Info |
| 2C-TFM (hydrochloride) | A 2C compound with a para-trifluoromethyl substitution. It is a potent ago… | 10 mg | 14471-10 | More Info |
| 2C-TFM (hydrochloride) | A 2C compound with a para-trifluoromethyl substitution. It is a potent ago… | 5 mg | 14471-5 | More Info |
| 2C-T (hydrochloride) | A member of a family of 2,5-dimethoxy phenethylamines, substituted on the… | 10 mg | 13957-10 | More Info |
| 2C-T (hydrochloride) | A member of a family of 2,5-dimethoxy phenethylamines, substituted on the… | 5 mg | 13957-5 | More Info |
| 2C-T (hydrochloride) | A member of a family of 2,5-dimethoxy phenethylamines, substituted on the… | 50 mg | 13957-50 | More Info |
| 2C-T-2 (hydrochloride) | A member of a family of 2,5-dimethoxy phenethylamines, substituted on the… | 10 mg | 11891-10 | More Info |
| 2C-T-2 (hydrochloride) | A member of a family of 2,5-dimethoxy phenethylamines, substituted on the… | 5 mg | 11891-5 | More Info |
| 2C-T-2 (hydrochloride) | A member of a family of 2,5-dimethoxy phenethylamines, substituted on the… | 50 mg | 11891-50 | More Info |
| 2C-T-4 (hydrochloride) | A member of a family of 2,5-dimethoxy phenethylamines, substituted on the… | 10 mg | 11892-10 | More Info |
| 2C-T-4 (hydrochloride) | A member of a family of 2,5-dimethoxy phenethylamines, substituted on the… | 5 mg | 11892-5 | More Info |
| 2C-T-4 (hydrochloride) | A member of a family of 2,5-dimethoxy phenethylamines, substituted on the… | 50 mg | 11892-50 | More Info |
| 2C-T-7 (hydrochloride) | A 2,5-dimethoxy phenethylamine with a propylthio group in the four positio… | 10 mg | 11200-10 | More Info |
| 2C-T-7 (hydrochloride) | A 2,5-dimethoxy phenethylamine with a propylthio group in the four positio… | 5 mg | 11200-5 | More Info |
| 2C-T-7 (hydrochloride) | A 2,5-dimethoxy phenethylamine with a propylthio group in the four positio… | 50 mg | 11200-50 | More Info |
| 2C-T-2 (hydrochloride) (exempt preparation) | A member of a family of 2,5-dimethoxy phenethylamines, substituted on the… | 1 mg | 15681-1 | More Info |
| 2C-T-4 (hydrochloride) (exempt preparation) | A member of a family of 2,5-dimethoxy phenethylamines, substituted on the… | 1 mg | 15719-1 | More Info |
| 2C-T-7 (hydrochloride) (exempt preparation) | A 2,5-dimethoxy phenethylamine with a propylthio group in the four positio… | 1 mg | 15672-1 | More Info |
| CTOP (trifluoroacetate salt) | An antagonist of the μ-opioid receptor (IC50 = 2.8 nM); selective for &… | 1 mg | 27377-1 | More Info |
| CTOP (trifluoroacetate salt) | An antagonist of the μ-opioid receptor (IC50 = 2.8 nM); selective for &… | 10 mg | 27377-10 | More Info |
| CTOP (trifluoroacetate salt) | An antagonist of the μ-opioid receptor (IC50 = 2.8 nM); selective for &… | 5 mg | 27377-5 | More Info |
| 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 |
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
Return to Profile