CP94 |
An iron chelator; enhances protoporphyrin IX photobleaching and decreases… |
25 mg |
33323-25 |
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CP94 |
An iron chelator; enhances protoporphyrin IX photobleaching and decreases… |
5 mg |
33323-5 |
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CP 105,696 |
A LTB4 receptor antagonist (IC50 = 8.42 nM for the high-affinity receptor… |
1 mg |
17620-1 |
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CP 105,696 |
A LTB4 receptor antagonist (IC50 = 8.42 nM for the high-affinity receptor… |
10 mg |
17620-10 |
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CP 105,696 |
A LTB4 receptor antagonist (IC50 = 8.42 nM for the high-affinity receptor… |
25 mg |
17620-25 |
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CP 105,696 |
A LTB4 receptor antagonist (IC50 = 8.42 nM for the high-affinity receptor… |
5 mg |
17620-5 |
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CP-4 |
A fluorescent probe for mesenchymal stem cells; abs / em = 577 / 617 nm, r… |
1 mg |
39984-1 |
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CP-4 |
A fluorescent probe for mesenchymal stem cells; abs / em = 577 / 617 nm, r… |
10 mg |
39984-10 |
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CP-4 |
A fluorescent probe for mesenchymal stem cells; abs / em = 577 / 617 nm, r… |
25 mg |
39984-25 |
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CP-4 |
A fluorescent probe for mesenchymal stem cells; abs / em = 577 / 617 nm, r… |
5 mg |
39984-5 |
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CPCCOEt |
A low affinity, selective, non-competitive antagonist of mGluR1b (IC50 = 6… |
1 mg |
21486-1 |
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CPCCOEt |
A low affinity, selective, non-competitive antagonist of mGluR1b (IC50 = 6… |
10 mg |
21486-10 |
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CPCCOEt |
A low affinity, selective, non-competitive antagonist of mGluR1b (IC50 = 6… |
5 mg |
21486-5 |
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CP 47,497-C6-homolog |
An analog of CP 47,497; intended for research and forensic applications |
1 mg |
9001448-1 |
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CP 47,497-C6-homolog |
An analog of CP 47,497; intended for research and forensic applications |
5 mg |
9001448-5 |
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CP 47,497-C9-homolog |
An analog of CP 47,497; intended for research and forensic applications |
1 mg |
9001449-1 |
More Info
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CP 47,497-C9-homolog |
An analog of CP 47,497; intended for research and forensic applications |
5 mg |
9001449-5 |
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CP 47,497-C8-homolog C-8-hydroxy metabolite |
A potential metabolite of CP 47,497-C8-homolog; intended for research and… |
1 mg |
9000773-1 |
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CP 47,497-C8-homolog C-8-hydroxy metabolite |
A potential metabolite of CP 47,497-C8-homolog; intended for research and… |
100 µg |
9000773-100 |
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CP 47,497-C8-homolog C-8-hydroxy metabolite |
A potential metabolite of CP 47,497-C8-homolog; intended for research and… |
500 µg |
9000773-500 |
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CpdA |
A non-steroidal selective glucocorticoid receptor modulator; contradictory… |
10 mg |
21438-10 |
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CpdA |
A non-steroidal selective glucocorticoid receptor modulator; contradictory… |
100 mg |
21438-100 |
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CpdA |
A non-steroidal selective glucocorticoid receptor modulator; contradictory… |
25 mg |
21438-25 |
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CpdA |
A non-steroidal selective glucocorticoid receptor modulator; contradictory… |
50 mg |
21438-50 |
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8-cPeT NAD+ (sodium salt) |
A derivative of NAD+; has been used in the screening of analog-sensitive P… |
800 µg |
38480-800 |
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(-)-CP 47,497 (exempt preparation) |
A bicyclic CB analog with potent analgesic activity; comparable or more po… |
1 mg |
13218-1 |
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(-)-CP 47,497 (exempt preparation) |
A bicyclic CB analog with potent analgesic activity; comparable or more po… |
5 mg |
13218-5 |
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(+)-CP 47,497 (exempt preparation) |
A bicyclic CB analog with potent analgesic activity; comparable or more po… |
1 mg |
13219-1 |
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(+)-CP 47,497 (exempt preparation) |
A bicyclic CB analog with potent analgesic activity; comparable or more po… |
5 mg |
13219-5 |
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CPHPC |
An inhibitor of the protein-protein interaction between SAP and amyloid fi… |
10 mg |
75500-10 |
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CPHPC |
An inhibitor of the protein-protein interaction between SAP and amyloid fi… |
5 mg |
75500-5 |
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CPHPC |
An inhibitor of the protein-protein interaction between SAP and amyloid fi… |
50 mg |
75500-50 |
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2C-P (hydrochloride) |
A member of a family of 2,5-dimethoxy-phenethylamines, substituted on the… |
10 mg |
11696-10 |
More Info
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2C-P (hydrochloride) |
A member of a family of 2,5-dimethoxy-phenethylamines, substituted on the… |
5 mg |
11696-5 |
More Info
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2C-P (hydrochloride) |
A member of a family of 2,5-dimethoxy-phenethylamines, substituted on the… |
50 mg |
11696-50 |
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3C-P (hydrochloride) |
A phenethylamine with structural similarity to amphetamine and proscaline |
1 mg |
14954-1 |
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3C-P (hydrochloride) |
A phenethylamine with structural similarity to amphetamine and proscaline |
5 mg |
14954-5 |
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CP 100,356 (hydrochloride) |
A P-glycoprotein inhibitor (IC50 = 0.5 µM); selective for P-gp over… |
1 mg |
32853-1 |
More Info
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CP 100,356 (hydrochloride) |
A P-glycoprotein inhibitor (IC50 = 0.5 µM); selective for P-gp over… |
10 mg |
32853-10 |
More Info
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CP 100,356 (hydrochloride) |
A P-glycoprotein inhibitor (IC50 = 0.5 µM); selective for P-gp over… |
5 mg |
32853-5 |
More Info
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CP 154,526 (hydrochloride) |
An antagonist of CRF1 (Ki = 2.7 nM); selective for CRF1 over CRF2 (Ki = >1… |
1 mg |
20732-1 |
More Info
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CP 154,526 (hydrochloride) |
An antagonist of CRF1 (Ki = 2.7 nM); selective for CRF1 over CRF2 (Ki = >1… |
10 mg |
20732-10 |
More Info
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CP 154,526 (hydrochloride) |
An antagonist of CRF1 (Ki = 2.7 nM); selective for CRF1 over CRF2 (Ki = >1… |
5 mg |
20732-5 |
More Info
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CP 154,526 (hydrochloride) |
An antagonist of CRF1 (Ki = 2.7 nM); selective for CRF1 over CRF2 (Ki = >1… |
500 µg |
20732-500 |
More Info
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CP 24,879 (hydrochloride) |
A Δ5/Δ6 desaturase inhibitor; reduces liver arachidonate conte… |
1 mg |
10120-1 |
More Info
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CP 24,879 (hydrochloride) |
A Δ5/Δ6 desaturase inhibitor; reduces liver arachidonate conte… |
10 mg |
10120-10 |
More Info
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CP 24,879 (hydrochloride) |
A Δ5/Δ6 desaturase inhibitor; reduces liver arachidonate conte… |
5 mg |
10120-5 |
More Info
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CP 24,879 (hydrochloride) |
A Δ5/Δ6 desaturase inhibitor; reduces liver arachidonate conte… |
50 mg |
10120-50 |
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CP 31,398 (hydrochloride) |
A p53 stabilizing agent; increases active mutant p53 and p53 reporter gene… |
1 mg |
27455-1 |
More Info
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CP 31,398 (hydrochloride) |
A p53 stabilizing agent; increases active mutant p53 and p53 reporter gene… |
10 mg |
27455-10 |
More Info
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CP 31,398 (hydrochloride) |
A p53 stabilizing agent; increases active mutant p53 and p53 reporter gene… |
5 mg |
27455-5 |
More Info
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CP 809,101 (hydrochloride) |
A potent 5-HT2C receptor agonist; selective for human 5-HT2C and rat 5-HT2… |
10 mg |
33283-10 |
More Info
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CP 809,101 (hydrochloride) |
A potent 5-HT2C receptor agonist; selective for human 5-HT2C and rat 5-HT2… |
25 mg |
33283-25 |
More Info
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CP 809,101 (hydrochloride) |
A potent 5-HT2C receptor agonist; selective for human 5-HT2C and rat 5-HT2… |
5 mg |
33283-5 |
More Info
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CP 809,101 (hydrochloride) |
A potent 5-HT2C receptor agonist; selective for human 5-HT2C and rat 5-HT2… |
50 mg |
33283-50 |
More Info
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CP 93,129 (hydrochloride) |
A 5-HT1B receptor agonist; selectively binds 5-HT1B over 5-HT1A, 5-HT1C, 5… |
1 mg |
34548-1 |
More Info
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CP 93,129 (hydrochloride) |
A 5-HT1B receptor agonist; selectively binds 5-HT1B over 5-HT1A, 5-HT1C, 5… |
10 mg |
34548-10 |
More Info
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CP 93,129 (hydrochloride) |
A 5-HT1B receptor agonist; selectively binds 5-HT1B over 5-HT1A, 5-HT1C, 5… |
25 mg |
34548-25 |
More Info
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CP 93,129 (hydrochloride) |
A 5-HT1B receptor agonist; selectively binds 5-HT1B over 5-HT1A, 5-HT1C, 5… |
5 mg |
34548-5 |
More Info
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CP 94,253 (hydrochloride) |
A 5-HT1B agonist (Ki = 2 nM in a radioligand binding assay); selective for… |
10 mg |
29486-10 |
More Info
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CP 94,253 (hydrochloride) |
A 5-HT1B agonist (Ki = 2 nM in a radioligand binding assay); selective for… |
25 mg |
29486-25 |
More Info
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CP 94,253 (hydrochloride) |
A 5-HT1B agonist (Ki = 2 nM in a radioligand binding assay); selective for… |
5 mg |
29486-5 |
More Info
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CP 945,598 (hydrochloride) |
A selective CB1 receptor antagonist (Ki = 0.7 nM); reverses cannabinoid ag… |
1 mg |
11955-1 |
More Info
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CP 945,598 (hydrochloride) |
A selective CB1 receptor antagonist (Ki = 0.7 nM); reverses cannabinoid ag… |
10 mg |
11955-10 |
More Info
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CP 945,598 (hydrochloride) |
A selective CB1 receptor antagonist (Ki = 0.7 nM); reverses cannabinoid ag… |
25 mg |
11955-25 |
More Info
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CP 945,598 (hydrochloride) |
A selective CB1 receptor antagonist (Ki = 0.7 nM); reverses cannabinoid ag… |
5 mg |
11955-5 |
More Info
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CP 99,994 (hydrochloride) |
A nonpeptide NK1 receptor antagonist (Ki = 0.25 nM in a radioligand bindin… |
1 mg |
27669-1 |
More Info
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CP 99,994 (hydrochloride) |
A nonpeptide NK1 receptor antagonist (Ki = 0.25 nM in a radioligand bindin… |
10 mg |
27669-10 |
More Info
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CP 99,994 (hydrochloride) |
A nonpeptide NK1 receptor antagonist (Ki = 0.25 nM in a radioligand bindin… |
5 mg |
27669-5 |
More Info
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CP 339,818 (hydrochloride) |
An inhibitor of Kv1.3 and Kv1.4 (IC50s = 0.23 and 0.3 µM, respective… |
10 mg |
40766-10 |
More Info
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CP 339,818 (hydrochloride) |
An inhibitor of Kv1.3 and Kv1.4 (IC50s = 0.23 and 0.3 µM, respective… |
25 mg |
40766-25 |
More Info
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CP 339,818 (hydrochloride) |
An inhibitor of Kv1.3 and Kv1.4 (IC50s = 0.23 and 0.3 µM, respective… |
5 mg |
40766-5 |
More Info
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CP 339,818 (hydrochloride) |
An inhibitor of Kv1.3 and Kv1.4 (IC50s = 0.23 and 0.3 µM, respective… |
50 mg |
40766-50 |
More Info
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2C-P (hydrochloride) (exempt preparation) |
A member of a family of 2,5-dimethoxy-phenethylamines, substituted on the… |
1 mg |
15718-1 |
More Info
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C18 Phytoceramide-d3 (t18:0/18:0-d3) |
An internal standard for the quantification of C18 phytoceramide by GC- or… |
1 mg |
27199-1 |
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