CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 839 of 865
Non-Antibody Products
Page 839 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Velneperit | An antagonist of NPY receptor Y5 (Ki = 5.3 nM); selective for Y5 over Y1,… | 10 mg | 33850-10 | More Info |
| Velneperit | An antagonist of NPY receptor Y5 (Ki = 5.3 nM); selective for Y5 over Y1,… | 25 mg | 33850-25 | More Info |
| Velneperit | An antagonist of NPY receptor Y5 (Ki = 5.3 nM); selective for Y5 over Y1,… | 5 mg | 33850-5 | More Info |
| Velpatasvir | An NS5A inhibitor; inhibits replication of HCV genotypes 1-6 (EC50s = 6-13… | 10 mg | 21280-10 | More Info |
| Velpatasvir | An NS5A inhibitor; inhibits replication of HCV genotypes 1-6 (EC50s = 6-13… | 100 mg | 21280-100 | More Info |
| Velpatasvir | An NS5A inhibitor; inhibits replication of HCV genotypes 1-6 (EC50s = 6-13… | 250 mg | 21280-250 | More Info |
| Velpatasvir | An NS5A inhibitor; inhibits replication of HCV genotypes 1-6 (EC50s = 6-13… | 50 mg | 21280-50 | More Info |
| Venturicidin A | A macrolide antibiotic with antifungal activity; also cytotoxic against tr… | 1 mg | 15377-1 | More Info |
| Venturicidin A | A macrolide antibiotic with antifungal activity; also cytotoxic against tr… | 5 mg | 15377-5 | More Info |
| Venturicidin B | A bacterial metabolite | 1 mg | 25478-1 | More Info |
| Venturicidin B | A bacterial metabolite | 250 µg | 25478-250 | More Info |
| VER-155008 | An inhibitor of Hsp70 (IC50 = 0.5 µM) that is selective over Hsp90;… | 10 mg | 17257-10 | More Info |
| VER-155008 | An inhibitor of Hsp70 (IC50 = 0.5 µM) that is selective over Hsp90;… | 25 mg | 17257-25 | More Info |
| VER-155008 | An inhibitor of Hsp70 (IC50 = 0.5 µM) that is selective over Hsp90;… | 5 mg | 17257-5 | More Info |
| VER-155008 | An inhibitor of Hsp70 (IC50 = 0.5 µM) that is selective over Hsp90;… | 50 mg | 17257-50 | More Info |
| VER-246608 | A pan-PDHK inhibitor (IC50s = 35, 84, 40, and 91 nM for PDHK1, -2, -3, and… | 1 mg | 19182-1 | More Info |
| VER-246608 | A pan-PDHK inhibitor (IC50s = 35, 84, 40, and 91 nM for PDHK1, -2, -3, and… | 10 mg | 19182-10 | More Info |
| VER-246608 | A pan-PDHK inhibitor (IC50s = 35, 84, 40, and 91 nM for PDHK1, -2, -3, and… | 25 mg | 19182-25 | More Info |
| VER-246608 | A pan-PDHK inhibitor (IC50s = 35, 84, 40, and 91 nM for PDHK1, -2, -3, and… | 5 mg | 19182-5 | More Info |
| VER-49009 | An Hsp90 inhibitor with an IC50 value of 47 nM; induces the expression of… | 1 mg | 13131-1 | More Info |
| VER-49009 | An Hsp90 inhibitor with an IC50 value of 47 nM; induces the expression of… | 10 mg | 13131-10 | More Info |
| VER-49009 | An Hsp90 inhibitor with an IC50 value of 47 nM; induces the expression of… | 5 mg | 13131-5 | More Info |
| VER-49009 | An Hsp90 inhibitor with an IC50 value of 47 nM; induces the expression of… | 500 µg | 13131-500 | More Info |
| VER-50589 | An isoxazole compound that inhibits Hsp90 with an IC50 value of 21 nM; pro… | 1 mg | 13132-1 | More Info |
| VER-50589 | An isoxazole compound that inhibits Hsp90 with an IC50 value of 21 nM; pro… | 5 mg | 13132-5 | More Info |
| VER-50589 | An isoxazole compound that inhibits Hsp90 with an IC50 value of 21 nM; pro… | 500 µg | 13132-500 | More Info |
| Verapamil (hydrochloride) | The prototypical blocker of L-type calcium channels that produces excitati… | 1 g | 14288-1 | More Info |
| Verapamil (hydrochloride) | The prototypical blocker of L-type calcium channels that produces excitati… | 10 g | 14288-10 | More Info |
| Verapamil (hydrochloride) | The prototypical blocker of L-type calcium channels that produces excitati… | 5 g | 14288-5 | More Info |
| Veratramine | An analog of cyclopamine that inhibits the Hh signaling-dependent prolifer… | 10 mg | 11724-10 | More Info |
| Veratramine | An analog of cyclopamine that inhibits the Hh signaling-dependent prolifer… | 25 mg | 11724-25 | More Info |
| Veratramine | An analog of cyclopamine that inhibits the Hh signaling-dependent prolifer… | 5 mg | 11724-5 | More Info |
| Veratramine | An analog of cyclopamine that inhibits the Hh signaling-dependent prolifer… | 50 mg | 11724-50 | More Info |
| Veratrosine | A steroidal alkaloid with diverse biological activities; inhibits Hh signa… | 1 mg | 34617-1 | More Info |
| Veratrosine | A steroidal alkaloid with diverse biological activities; inhibits Hh signa… | 10 mg | 34617-10 | More Info |
| Veratrosine | A steroidal alkaloid with diverse biological activities; inhibits Hh signa… | 25 mg | 34617-25 | More Info |
| Veratrosine | A steroidal alkaloid with diverse biological activities; inhibits Hh signa… | 5 mg | 34617-5 | More Info |
| Verbascoside | A natural phenylpropanoid glucoside; inhibits PKC (IC50 = 25 µM); in… | 1 mg | 24965-1 | More Info |
| Verbascoside | A natural phenylpropanoid glucoside; inhibits PKC (IC50 = 25 µM); in… | 10 mg | 24965-10 | More Info |
| Verbascoside | A natural phenylpropanoid glucoside; inhibits PKC (IC50 = 25 µM); in… | 25 mg | 24965-25 | More Info |
| Verbascoside | A natural phenylpropanoid glucoside; inhibits PKC (IC50 = 25 µM); in… | 5 mg | 24965-5 | More Info |
| Verbenalin | An iridoid glucoside; inhibits the activities of COX-1 and COX-2 by 37 and… | 1 mg | 34663-1 | More Info |
| Verbenalin | An iridoid glucoside; inhibits the activities of COX-1 and COX-2 by 37 and… | 10 mg | 34663-10 | More Info |
| Verbenalin | An iridoid glucoside; inhibits the activities of COX-1 and COX-2 by 37 and… | 25 mg | 34663-25 | More Info |
| Verbenalin | An iridoid glucoside; inhibits the activities of COX-1 and COX-2 by 37 and… | 5 mg | 34663-5 | More Info |
| Vercirnon | An antagonist of CCR9 (IC50 = 5.4 nM); selective for CCR9 over CCR1-12 and… | 1 mg | 23131-1 | More Info |
| Vercirnon | An antagonist of CCR9 (IC50 = 5.4 nM); selective for CCR9 over CCR1-12 and… | 5 mg | 23131-5 | More Info |
| Verdinexor | An inhibitor of XPO1 / CRM1 with anticancer and antiviral activities; inhi… | 1 mg | 26171-1 | More Info |
| Verdinexor | An inhibitor of XPO1 / CRM1 with anticancer and antiviral activities; inhi… | 10 mg | 26171-10 | More Info |
| Verdinexor | An inhibitor of XPO1 / CRM1 with anticancer and antiviral activities; inhi… | 5 mg | 26171-5 | More Info |
| Verdiperstat | An irreversible inhibitor of MPO (IC50 = 630 nM); selective for MPO over a… | 10 mg | 37333-10 | More Info |
| Verdiperstat | An irreversible inhibitor of MPO (IC50 = 630 nM); selective for MPO over a… | 25 mg | 37333-25 | More Info |
| Verdiperstat | An irreversible inhibitor of MPO (IC50 = 630 nM); selective for MPO over a… | 5 mg | 37333-5 | More Info |
| Verdiperstat | An irreversible inhibitor of MPO (IC50 = 630 nM); selective for MPO over a… | 50 mg | 37333-50 | More Info |
| Vericiguat | A stimulator of sGC; stimulates the formation of cGMP in CHO cells express… | 10 mg | 35253-10 | More Info |
| Vericiguat | A stimulator of sGC; stimulates the formation of cGMP in CHO cells express… | 25 mg | 35253-25 | More Info |
| Vericiguat | A stimulator of sGC; stimulates the formation of cGMP in CHO cells express… | 5 mg | 35253-5 | More Info |
| Vericiguat | A stimulator of sGC; stimulates the formation of cGMP in CHO cells express… | 50 mg | 35253-50 | More Info |
| Verinurad | A URAT1 inhibitor (IC50 = 0.025 µM for the human transporter); selec… | 10 mg | 29667-10 | More Info |
| Verinurad | A URAT1 inhibitor (IC50 = 0.025 µM for the human transporter); selec… | 100 mg | 29667-100 | More Info |
| Verinurad | A URAT1 inhibitor (IC50 = 0.025 µM for the human transporter); selec… | 5 mg | 29667-5 | More Info |
| Verinurad | A URAT1 inhibitor (IC50 = 0.025 µM for the human transporter); selec… | 50 mg | 29667-50 | More Info |
| Verrucarin A | A macrocyclic trichothecene with diverse biological activities; induces ap… | 1 mg | 29652-1 | More Info |
| Verrucarin J | A macrocyclic trichothecene with fungicidal and anticancer activities; act… | 1 mg | 40815-1 | More Info |
| Verrucofortine | A fungal metabolite | 25 mg | 28062-25 | More Info |
| Verrucofortine | A fungal metabolite | 5 mg | 28062-5 | More Info |
| Verruculogen | A tremorgenic mycotoxin that selectively inhibits the activation of Maxi-K… | 1 mg | 11351-1 | More Info |
| Verruculogen | A tremorgenic mycotoxin that selectively inhibits the activation of Maxi-K… | 5 mg | 11351-5 | More Info |
| Verteporfin | A photosensitizer used during photodynamic therapy to eliminate abnormal b… | 1 mg | 17334-1 | More Info |
| Verteporfin | A photosensitizer used during photodynamic therapy to eliminate abnormal b… | 10 mg | 17334-10 | More Info |
| Verteporfin | A photosensitizer used during photodynamic therapy to eliminate abnormal b… | 25 mg | 17334-25 | More Info |
| Verteporfin | A photosensitizer used during photodynamic therapy to eliminate abnormal b… | 5 mg | 17334-5 | More Info |
| Verubecestat | An inhibitor of BACE1 and BACE2 (Kis = 2.2 and 0.38 nM, respectively) | 1 mg | 21115-1 | More Info |
| Verubecestat | An inhibitor of BACE1 and BACE2 (Kis = 2.2 and 0.38 nM, respectively) | 10 mg | 21115-10 | More Info |
| Verubecestat | An inhibitor of BACE1 and BACE2 (Kis = 2.2 and 0.38 nM, respectively) | 25 mg | 21115-25 | 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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