CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 845 of 865
Non-Antibody Products
Page 845 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| VU0240551 | A KCC2 inhibitor (IC50 = 568 nM); selectively inhibits KCC2 over NKCC1 (IC… | 5 mg | 29790-5 | More Info |
| VU0240551 | A KCC2 inhibitor (IC50 = 568 nM); selectively inhibits KCC2 over NKCC1 (IC… | 50 mg | 29790-50 | More Info |
| VU0255035 | A selective, competitive orthosteric antagonist of the muscarinic M1 recep… | 10 mg | 19353-10 | More Info |
| VU0255035 | A selective, competitive orthosteric antagonist of the muscarinic M1 recep… | 50 mg | 19353-50 | More Info |
| VU0357121 | A positive allosteric modulator of mGluR5 (EC50 = 33 nM); selective for mG… | 10 mg | 22199-10 | More Info |
| VU0357121 | A positive allosteric modulator of mGluR5 (EC50 = 33 nM); selective for mG… | 25 mg | 22199-25 | More Info |
| VU0357121 | A positive allosteric modulator of mGluR5 (EC50 = 33 nM); selective for mG… | 5 mg | 22199-5 | More Info |
| VU0357121 | A positive allosteric modulator of mGluR5 (EC50 = 33 nM); selective for mG… | 50 mg | 22199-50 | More Info |
| VU0359595 | A highly selective inhibitor of PLD1 (IC50 = 3.7 nM) versus PLD2 (IC50 = 6… | 1 mg | 10955-1 | More Info |
| VU0359595 | A highly selective inhibitor of PLD1 (IC50 = 3.7 nM) versus PLD2 (IC50 = 6… | 10 mg | 10955-10 | More Info |
| VU0359595 | A highly selective inhibitor of PLD1 (IC50 = 3.7 nM) versus PLD2 (IC50 = 6… | 25 mg | 10955-25 | More Info |
| VU0359595 | A highly selective inhibitor of PLD1 (IC50 = 3.7 nM) versus PLD2 (IC50 = 6… | 5 mg | 10955-5 | More Info |
| VU0360223 | A selective, negative allosteric modulator of the mGlu5 (IC50 = 61 nM; Ki… | 1 mg | 11995-1 | More Info |
| VU0360223 | A selective, negative allosteric modulator of the mGlu5 (IC50 = 61 nM; Ki… | 10 mg | 11995-10 | More Info |
| VU0360223 | A selective, negative allosteric modulator of the mGlu5 (IC50 = 61 nM; Ki… | 5 mg | 11995-5 | More Info |
| VU0360223 | A selective, negative allosteric modulator of the mGlu5 (IC50 = 61 nM; Ki… | 50 mg | 11995-50 | More Info |
| VU0361737 | A selective PAM of mGluR4, displaying EC50 values of 110 and 240 nM for ra… | 1 mg | 16295-1 | More Info |
| VU0361737 | A selective PAM of mGluR4, displaying EC50 values of 110 and 240 nM for ra… | 10 mg | 16295-10 | More Info |
| VU0361737 | A selective PAM of mGluR4, displaying EC50 values of 110 and 240 nM for ra… | 5 mg | 16295-5 | More Info |
| VU0364439 | A positive allosteric modulator of mGluR4; potentiates glutamate responses… | 1 mg | 16296-1 | More Info |
| VU0364439 | A positive allosteric modulator of mGluR4; potentiates glutamate responses… | 10 mg | 16296-10 | More Info |
| VU0364439 | A positive allosteric modulator of mGluR4; potentiates glutamate responses… | 5 mg | 16296-5 | More Info |
| VU0364439 | A positive allosteric modulator of mGluR4; potentiates glutamate responses… | 50 mg | 16296-50 | More Info |
| VU0364770 | A positive allosteric modulator of metabotropic glutamate receptor 4 (mGlu… | 10 mg | 22927-10 | More Info |
| VU0364770 | A positive allosteric modulator of metabotropic glutamate receptor 4 (mGlu… | 25 mg | 22927-25 | More Info |
| VU0364770 | A positive allosteric modulator of metabotropic glutamate receptor 4 (mGlu… | 5 mg | 22927-5 | More Info |
| VU0364770 | A positive allosteric modulator of metabotropic glutamate receptor 4 (mGlu… | 50 mg | 22927-50 | More Info |
| VU0365114 | A positive allosteric modulator of muscarinic M5 receptors; increases ACh-… | 10 mg | 33709-10 | More Info |
| VU0365114 | A positive allosteric modulator of muscarinic M5 receptors; increases ACh-… | 100 mg | 33709-100 | More Info |
| VU0365114 | A positive allosteric modulator of muscarinic M5 receptors; increases ACh-… | 50 mg | 33709-50 | More Info |
| VU0409551 | An mGluR5 PAM; induces calcium mobilization in HEK293 cells expressing hum… | 1 mg | 18042-1 | More Info |
| VU0409551 | An mGluR5 PAM; induces calcium mobilization in HEK293 cells expressing hum… | 10 mg | 18042-10 | More Info |
| VU0409551 | An mGluR5 PAM; induces calcium mobilization in HEK293 cells expressing hum… | 25 mg | 18042-25 | More Info |
| VU0409551 | An mGluR5 PAM; induces calcium mobilization in HEK293 cells expressing hum… | 5 mg | 18042-5 | More Info |
| VU0467154 | A positive allosteric modulator of the M4 muscarinic acetylcholine recepto… | 1 mg | 25555-1 | More Info |
| VU0467154 | A positive allosteric modulator of the M4 muscarinic acetylcholine recepto… | 10 mg | 25555-10 | More Info |
| VU0467154 | A positive allosteric modulator of the M4 muscarinic acetylcholine recepto… | 25 mg | 25555-25 | More Info |
| VU0467154 | A positive allosteric modulator of the M4 muscarinic acetylcholine recepto… | 5 mg | 25555-5 | More Info |
| VU0483605 | A selective mGluR1 PAM (EC50s = 0.39 and 0.36 µM for human and rat r… | 1 mg | 16941-1 | More Info |
| VU0483605 | A selective mGluR1 PAM (EC50s = 0.39 and 0.36 µM for human and rat r… | 10 mg | 16941-10 | More Info |
| VU0483605 | A selective mGluR1 PAM (EC50s = 0.39 and 0.36 µM for human and rat r… | 5 mg | 16941-5 | More Info |
| VU0661013 | An Mcl-1 inhibitor (Ki = 97 pM); selective for Mcl-1 over Bcl-xL and Bcl-2… | 1 mg | 39524-1 | More Info |
| VU0661013 | An Mcl-1 inhibitor (Ki = 97 pM); selective for Mcl-1 over Bcl-xL and Bcl-2… | 10 mg | 39524-10 | More Info |
| VU0661013 | An Mcl-1 inhibitor (Ki = 97 pM); selective for Mcl-1 over Bcl-xL and Bcl-2… | 5 mg | 39524-5 | More Info |
| VUF 10166 | A 5-HT3A antagonist (Ki = 0.04 nM); selective for 5-HT3A over 5-HT3AB rece… | 10 mg | 31423-10 | More Info |
| VUF 10166 | A 5-HT3A antagonist (Ki = 0.04 nM); selective for 5-HT3A over 5-HT3AB rece… | 100 mg | 31423-100 | More Info |
| VUF 10166 | A 5-HT3A antagonist (Ki = 0.04 nM); selective for 5-HT3A over 5-HT3AB rece… | 25 mg | 31423-25 | More Info |
| VUF 10166 | A 5-HT3A antagonist (Ki = 0.04 nM); selective for 5-HT3A over 5-HT3AB rece… | 50 mg | 31423-50 | More Info |
| VUF 5574 | An adenosine A3 receptor antagonist (Ki = 4.03 nM for the recombinant huma… | 1 mg | 27676-1 | More Info |
| VUF 5574 | An adenosine A3 receptor antagonist (Ki = 4.03 nM for the recombinant huma… | 10 mg | 27676-10 | More Info |
| VUF 5574 | An adenosine A3 receptor antagonist (Ki = 4.03 nM for the recombinant huma… | 5 mg | 27676-5 | More Info |
| VUF10460 | A histamine H4 receptor agonist (Kis = 5.01 and 14.13 for the human and ra… | 1 mg | 14665-1 | More Info |
| VUF10460 | A histamine H4 receptor agonist (Kis = 5.01 and 14.13 for the human and ra… | 10 mg | 14665-10 | More Info |
| VUF10460 | A histamine H4 receptor agonist (Kis = 5.01 and 14.13 for the human and ra… | 25 mg | 14665-25 | More Info |
| VUF10460 | A histamine H4 receptor agonist (Kis = 5.01 and 14.13 for the human and ra… | 5 mg | 14665-5 | More Info |
| VUF8430 (hydrobromide) | A histamine H4 receptor agonist (Ki = 31.6 nM); selective for histamine H4… | 1 mg | 27682-1 | More Info |
| VUF8430 (hydrobromide) | A histamine H4 receptor agonist (Ki = 31.6 nM); selective for histamine H4… | 10 mg | 27682-10 | More Info |
| VUF8430 (hydrobromide) | A histamine H4 receptor agonist (Ki = 31.6 nM); selective for histamine H4… | 25 mg | 27682-25 | More Info |
| VUF8430 (hydrobromide) | A histamine H4 receptor agonist (Ki = 31.6 nM); selective for histamine H4… | 5 mg | 27682-5 | More Info |
| VUF 11207 (trifluoroacetate salt) | A potent CXCR7 receptor agonist (EC50 = 1.6 nM for β-arrestin recruit… | 1 mg | 19812-1 | More Info |
| VUF 11207 (trifluoroacetate salt) | A potent CXCR7 receptor agonist (EC50 = 1.6 nM for β-arrestin recruit… | 10 mg | 19812-10 | More Info |
| VUF 11207 (trifluoroacetate salt) | A potent CXCR7 receptor agonist (EC50 = 1.6 nM for β-arrestin recruit… | 5 mg | 19812-5 | More Info |
| VU0134992 (hydrochloride) | An inhibitor of Kir4.1 (IC50 = 5.2 µM in a thallium flux assay); sel… | 10 mg | 37299-10 | More Info |
| VU0134992 (hydrochloride) | An inhibitor of Kir4.1 (IC50 = 5.2 µM in a thallium flux assay); sel… | 25 mg | 37299-25 | More Info |
| VU0134992 (hydrochloride) | An inhibitor of Kir4.1 (IC50 = 5.2 µM in a thallium flux assay); sel… | 5 mg | 37299-5 | More Info |
| VU0134992 (hydrochloride) | An inhibitor of Kir4.1 (IC50 = 5.2 µM in a thallium flux assay); sel… | 50 mg | 37299-50 | More Info |
| VU0357017 (hydrochloride) | A selective agonist of M1 mAChRs (Ki = 9.91 µM); selective for M1 ov… | 1 mg | 11939-1 | More Info |
| VU0357017 (hydrochloride) | A selective agonist of M1 mAChRs (Ki = 9.91 µM); selective for M1 ov… | 10 mg | 11939-10 | More Info |
| VU0357017 (hydrochloride) | A selective agonist of M1 mAChRs (Ki = 9.91 µM); selective for M1 ov… | 25 mg | 11939-25 | More Info |
| VU0357017 (hydrochloride) | A selective agonist of M1 mAChRs (Ki = 9.91 µM); selective for M1 ov… | 5 mg | 11939-5 | More Info |
| VU0360172 (hydrochloride) | A positive allosteric modulator of mGluR5 (Ki = 195 nM); selective for mGl… | 10 mg | 22074-10 | More Info |
| VU0360172 (hydrochloride) | A positive allosteric modulator of mGluR5 (Ki = 195 nM); selective for mGl… | 25 mg | 22074-25 | More Info |
| VU0360172 (hydrochloride) | A positive allosteric modulator of mGluR5 (Ki = 195 nM); selective for mGl… | 5 mg | 22074-5 | More Info |
| VU0360172 (hydrochloride) | A positive allosteric modulator of mGluR5 (Ki = 195 nM); selective for mGl… | 50 mg | 22074-50 | More Info |
| VU0469650 (hydrochloride) | A negative allosteric mGluR1 modulator; inhibits glutamate-induced calcium… | 1 mg | 32933-1 | 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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