CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 197 of 859
Non-Antibody Products
Page 197 of 859
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Curcumin (technical grade) | A yellow pigment with diverse biological activities; inhibits NO productio… | 5 g | 81025.1-5 | More Info |
| Curcumin (technical grade) | A yellow pigment with diverse biological activities; inhibits NO productio… | 50 g | 81025.1-50 | More Info |
| Curcumol | A sesquiterpene alcohol with diverse biological activities; a PAM of GABAA… | 10 mg | 26849-10 | More Info |
| Curcumol | A sesquiterpene alcohol with diverse biological activities; a PAM of GABAA… | 100 mg | 26849-100 | More Info |
| Curcumol | A sesquiterpene alcohol with diverse biological activities; a PAM of GABAA… | 25 mg | 26849-25 | More Info |
| Curcumol | A sesquiterpene alcohol with diverse biological activities; a PAM of GABAA… | 50 mg | 26849-50 | More Info |
| Curdione | A sesquiterpene with diverse biological activities; reduces the cytopathic… | 1 mg | 30365-1 | More Info |
| Curdione | A sesquiterpene with diverse biological activities; reduces the cytopathic… | 5 mg | 30365-5 | More Info |
| Curdione | A sesquiterpene with diverse biological activities; reduces the cytopathic… | 500 µg | 30365-500 | More Info |
| C6 Urea Ceramide | An inhibitor of neutral ceramidase; It increases total ceramide levels in… | 1 mg | 25491-1 | More Info |
| C6 Urea Ceramide | An inhibitor of neutral ceramidase; It increases total ceramide levels in… | 10 mg | 25491-10 | More Info |
| C6 Urea Ceramide | An inhibitor of neutral ceramidase; It increases total ceramide levels in… | 5 mg | 25491-5 | More Info |
| Curvularin | A fungal macrolactone that has cytotoxic activity against select cancer ce… | 1 mg | 21758-1 | More Info |
| Curvularin | A fungal macrolactone that has cytotoxic activity against select cancer ce… | 5 mg | 21758-5 | More Info |
| Curvulin | A phytotoxin reported to inhibit microtubule assembly and iNOS expression | 1 mg | 19609-1 | More Info |
| Curvulin | A phytotoxin reported to inhibit microtubule assembly and iNOS expression | 5 mg | 19609-5 | More Info |
| Curvulinic Acid | A fungal metabolite; inhibits C. bursa-pastoris seed germination, root gro… | 1 mg | 33094-1 | More Info |
| Curvulinic Acid | A fungal metabolite; inhibits C. bursa-pastoris seed germination, root gro… | 250 µg | 33094-250 | More Info |
| Cuspin-1 | A small molecule upregulator of SMN that has been shown in vitro to increa… | 10 mg | 18526-10 | More Info |
| Cuspin-1 | A small molecule upregulator of SMN that has been shown in vitro to increa… | 25 mg | 18526-25 | More Info |
| Cuspin-1 | A small molecule upregulator of SMN that has been shown in vitro to increa… | 5 mg | 18526-5 | More Info |
| Cuspin-1 | A small molecule upregulator of SMN that has been shown in vitro to increa… | 50 mg | 18526-50 | More Info |
| Custom Assay Development | Along with our extensive catalog of commercial assays, Cayman offers custo… | n/a | n/a | More Info |
| Custom Compound Libraries | Cayman Chemical offers generation of custom compound libraries. | n/a | n/a | More Info |
| CU-T12-9 | An agonist of TLR1 / 2; selective for TLR1 / 2 over TLR2 / 6 in a SEAP ass… | 1 mg | 32867-1 | More Info |
| CU-T12-9 | An agonist of TLR1 / 2; selective for TLR1 / 2 over TLR2 / 6 in a SEAP ass… | 10 mg | 32867-10 | More Info |
| CU-T12-9 | An agonist of TLR1 / 2; selective for TLR1 / 2 over TLR2 / 6 in a SEAP ass… | 5 mg | 32867-5 | More Info |
| CV-6209 (chloride) | A potent antagonist of the PAF receptor, inhibiting aggregation of rabbit… | 1 mg | 15955-1 | More Info |
| CV-6209 (chloride) | A potent antagonist of the PAF receptor, inhibiting aggregation of rabbit… | 5 mg | 15955-5 | More Info |
| CV-6209 (chloride) | A potent antagonist of the PAF receptor, inhibiting aggregation of rabbit… | 500 µg | 15955-500 | More Info |
| CV-6209-d5 | An internal standard for the quantification of CV-6209 by GC- or LC-MS | 1 mg | 9002895-1 | More Info |
| CV-6209-d5 | An internal standard for the quantification of CV-6209 by GC- or LC-MS | 250 µg | 9002895-250 | More Info |
| CV-6209-d5 | An internal standard for the quantification of CV-6209 by GC- or LC-MS | 500 µg | 9002895-500 | More Info |
| CVT-10216 | A selective, reversible inhibitor of ALDH2 (IC50 = 29 nM); reduces excessi… | 1 mg | 18318-1 | More Info |
| CVT-10216 | A selective, reversible inhibitor of ALDH2 (IC50 = 29 nM); reduces excessi… | 10 mg | 18318-10 | More Info |
| CVT-10216 | A selective, reversible inhibitor of ALDH2 (IC50 = 29 nM); reduces excessi… | 25 mg | 18318-25 | More Info |
| CVT-10216 | A selective, reversible inhibitor of ALDH2 (IC50 = 29 nM); reduces excessi… | 5 mg | 18318-5 | More Info |
| CVT-12012 | An SCD inhibitor (IC50 = 6.1 nM in HepG2 cells); dose-dependently reduces… | 1 mg | 27156-1 | More Info |
| CVT-12012 | An SCD inhibitor (IC50 = 6.1 nM in HepG2 cells); dose-dependently reduces… | 10 mg | 27156-10 | More Info |
| CVT-12012 | An SCD inhibitor (IC50 = 6.1 nM in HepG2 cells); dose-dependently reduces… | 25 mg | 27156-25 | More Info |
| CVT-12012 | An SCD inhibitor (IC50 = 6.1 nM in HepG2 cells); dose-dependently reduces… | 5 mg | 27156-5 | More Info |
| CVT-2738 | An active metabolite of ranolazine; inhibits increases in T-wave height an… | 1 g | 35003-1 | More Info |
| CVT-2738 | An active metabolite of ranolazine; inhibits increases in T-wave height an… | 250 mg | 35003-250 | More Info |
| CVT-2738 | An active metabolite of ranolazine; inhibits increases in T-wave height an… | 5 g | 35003-5 | More Info |
| CVT-2738 | An active metabolite of ranolazine; inhibits increases in T-wave height an… | 500 mg | 35003-500 | More Info |
| CVT-313 | A selective, competitive inhibitor of Cdk2 (IC50 = 0.5 µM in vitro);… | 1 mg | 21044-1 | More Info |
| CVT-313 | A selective, competitive inhibitor of Cdk2 (IC50 = 0.5 µM in vitro);… | 10 mg | 21044-10 | More Info |
| CVT-313 | A selective, competitive inhibitor of Cdk2 (IC50 = 0.5 µM in vitro);… | 5 mg | 21044-5 | More Info |
| CVT-6883 | An adenosine A2B receptor antagonist (Ki = 22 nM); selective for adenosine… | 1 mg | 33333-1 | More Info |
| CVT-6883 | An adenosine A2B receptor antagonist (Ki = 22 nM); selective for adenosine… | 10 mg | 33333-10 | More Info |
| CVT-6883 | An adenosine A2B receptor antagonist (Ki = 22 nM); selective for adenosine… | 25 mg | 33333-25 | More Info |
| CVT-6883 | An adenosine A2B receptor antagonist (Ki = 22 nM); selective for adenosine… | 5 mg | 33333-5 | More Info |
| CW069 | An inhibitor of KIFC / HSET (IC50 = 75 µM); increases the number of… | 1 mg | 22936-1 | More Info |
| CW069 | An inhibitor of KIFC / HSET (IC50 = 75 µM); increases the number of… | 10 mg | 22936-10 | More Info |
| CW069 | An inhibitor of KIFC / HSET (IC50 = 75 µM); increases the number of… | 5 mg | 22936-5 | More Info |
| CWHM12 | An inhibitor of αv integrins (IC50s = 1.8, 0.8, 61, 1.5, and 0.2 nM… | 1 mg | 19480-1 | More Info |
| CWHM12 | An inhibitor of αv integrins (IC50s = 1.8, 0.8, 61, 1.5, and 0.2 nM… | 10 mg | 19480-10 | More Info |
| CWHM12 | An inhibitor of αv integrins (IC50s = 1.8, 0.8, 61, 1.5, and 0.2 nM… | 25 mg | 19480-25 | More Info |
| CWHM12 | An inhibitor of αv integrins (IC50s = 1.8, 0.8, 61, 1.5, and 0.2 nM… | 5 mg | 19480-5 | More Info |
| CX-4945 | A potent, orally bioavailable inhibitor of casein kinase 2 (CK2; Ki = 0.38… | 1 mg | 16779-1 | More Info |
| CX-4945 | A potent, orally bioavailable inhibitor of casein kinase 2 (CK2; Ki = 0.38… | 10 mg | 16779-10 | More Info |
| CX-4945 | A potent, orally bioavailable inhibitor of casein kinase 2 (CK2; Ki = 0.38… | 5 mg | 16779-5 | More Info |
| CX-4945 | A potent, orally bioavailable inhibitor of casein kinase 2 (CK2; Ki = 0.38… | 500 µg | 16779-500 | More Info |
| CX-516 | An AMPA receptor modulator; increases the mean open time of AMPA receptors… | 10 mg | 14936-10 | More Info |
| CX-516 | An AMPA receptor modulator; increases the mean open time of AMPA receptors… | 25 mg | 14936-25 | More Info |
| CX-516 | An AMPA receptor modulator; increases the mean open time of AMPA receptors… | 5 mg | 14936-5 | More Info |
| CX-516 | An AMPA receptor modulator; increases the mean open time of AMPA receptors… | 50 mg | 14936-50 | More Info |
| CX-5461 | A selective inhibitor of RNA polymerase I-driven transcription of rRNA (IC… | 1 mg | 18392-1 | More Info |
| CX-5461 | A selective inhibitor of RNA polymerase I-driven transcription of rRNA (IC… | 10 mg | 18392-10 | More Info |
| CX-5461 | A selective inhibitor of RNA polymerase I-driven transcription of rRNA (IC… | 5 mg | 18392-5 | More Info |
| CX-5461 | A selective inhibitor of RNA polymerase I-driven transcription of rRNA (IC… | 50 mg | 18392-50 | More Info |
| CX-6258 | A potent, reversible, orally bioavailable inhibitor of Pim-1, -2, and -3 (… | 1 mg | 16245-1 | More Info |
| CX-6258 | A potent, reversible, orally bioavailable inhibitor of Pim-1, -2, and -3 (… | 10 mg | 16245-10 | More Info |
| CX-6258 | A potent, reversible, orally bioavailable inhibitor of Pim-1, -2, and -3 (… | 25 mg | 16245-25 | More Info |
| CX-6258 | A potent, reversible, orally bioavailable inhibitor of Pim-1, -2, and -3 (… | 5 mg | 16245-5 | 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
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