(+)-CP 101,606 |
An antagonist of NR2B subunit-containing NMDA receptors (Kd = 4.2 nM); sel… |
25 mg |
23884-25 |
More Info
|
(+)-CP 101,606 |
An antagonist of NR2B subunit-containing NMDA receptors (Kd = 4.2 nM); sel… |
5 mg |
23884-5 |
More Info
|
(+)-CP 47,497 |
A bicyclic CB analog with potent analgesic activity; comparable or more po… |
1 mg |
10910-1 |
More Info
|
(+)-CP 47,497 |
A bicyclic CB analog with potent analgesic activity; comparable or more po… |
5 mg |
10910-5 |
More Info
|
(+)-CP 55,940 |
An analytical reference standard that is structurally similar to known syn… |
1 mg |
13608-1 |
More Info
|
(+)-CP 55,940 |
An analytical reference standard that is structurally similar to known syn… |
5 mg |
13608-5 |
More Info
|
CP 226,269 |
A dopamine D4 receptor agonist; induces calcium flux in HEK293 cells co-ex… |
1 mg |
36493-1 |
More Info
|
CP 226,269 |
A dopamine D4 receptor agonist; induces calcium flux in HEK293 cells co-ex… |
10 mg |
36493-10 |
More Info
|
CP 226,269 |
A dopamine D4 receptor agonist; induces calcium flux in HEK293 cells co-ex… |
25 mg |
36493-25 |
More Info
|
CP 226,269 |
A dopamine D4 receptor agonist; induces calcium flux in HEK293 cells co-ex… |
5 mg |
36493-5 |
More Info
|
CP 316,819 |
An inhibitor of glycogen phosphorylase A (IC50 = 40 nM for the human liver… |
1 mg |
32856-1 |
More Info
|
CP 316,819 |
An inhibitor of glycogen phosphorylase A (IC50 = 40 nM for the human liver… |
5 mg |
32856-5 |
More Info
|
CP 346,086 |
An MTTP inhibitor (IC50 = 2 nM); inhibits ApoB and triglyceride secretion… |
1 mg |
39156-1 |
More Info
|
CP 346,086 |
An MTTP inhibitor (IC50 = 2 nM); inhibits ApoB and triglyceride secretion… |
10 mg |
39156-10 |
More Info
|
CP 346,086 |
An MTTP inhibitor (IC50 = 2 nM); inhibits ApoB and triglyceride secretion… |
25 mg |
39156-25 |
More Info
|
CP 346,086 |
An MTTP inhibitor (IC50 = 2 nM); inhibits ApoB and triglyceride secretion… |
5 mg |
39156-5 |
More Info
|
CP 376,395 |
A CRF1 antagonist (IC50 = 5.1 nM); inhibits adenylate cyclase activity sti… |
1 mg |
29188-1 |
More Info
|
CP 376,395 |
A CRF1 antagonist (IC50 = 5.1 nM); inhibits adenylate cyclase activity sti… |
10 mg |
29188-10 |
More Info
|
CP 376,395 |
A CRF1 antagonist (IC50 = 5.1 nM); inhibits adenylate cyclase activity sti… |
5 mg |
29188-5 |
More Info
|
CP 424,174 |
An inhibitor of stimulus-coupled IL-1β post-translational processing;… |
1 mg |
29675-1 |
More Info
|
CP 424,174 |
An inhibitor of stimulus-coupled IL-1β post-translational processing;… |
10 mg |
29675-10 |
More Info
|
CP 424,174 |
An inhibitor of stimulus-coupled IL-1β post-translational processing;… |
25 mg |
29675-25 |
More Info
|
CP 424,174 |
An inhibitor of stimulus-coupled IL-1β post-translational processing;… |
5 mg |
29675-5 |
More Info
|
CP 466,722 |
An ATM kinase inhibitor; inhibits ionizing radiation-induced ATM autophosp… |
1 mg |
25417-1 |
More Info
|
CP 466,722 |
An ATM kinase inhibitor; inhibits ionizing radiation-induced ATM autophosp… |
10 mg |
25417-10 |
More Info
|
CP 466,722 |
An ATM kinase inhibitor; inhibits ionizing radiation-induced ATM autophosp… |
25 mg |
25417-25 |
More Info
|
CP 466,722 |
An ATM kinase inhibitor; inhibits ionizing radiation-induced ATM autophosp… |
5 mg |
25417-5 |
More Info
|
CP 471,474 |
A broad-spectrum MMP inhibitor (IC50s = 0.7, 16, 13, and 0.9 nM for MMP-2,… |
1 mg |
29442-1 |
More Info
|
CP 471,474 |
A broad-spectrum MMP inhibitor (IC50s = 0.7, 16, 13, and 0.9 nM for MMP-2,… |
10 mg |
29442-10 |
More Info
|
CP 471,474 |
A broad-spectrum MMP inhibitor (IC50s = 0.7, 16, 13, and 0.9 nM for MMP-2,… |
5 mg |
29442-5 |
More Info
|
CP 544,326 |
A potent EP2 receptor agonist (IC50s = 10 and 15 nM for human and rat EP2,… |
1 mg |
22945-1 |
More Info
|
CP 544,326 |
A potent EP2 receptor agonist (IC50s = 10 and 15 nM for human and rat EP2,… |
10 mg |
22945-10 |
More Info
|
CP 544,326 |
A potent EP2 receptor agonist (IC50s = 10 and 15 nM for human and rat EP2,… |
25 mg |
22945-25 |
More Info
|
CP 544,326 |
A potent EP2 receptor agonist (IC50s = 10 and 15 nM for human and rat EP2,… |
5 mg |
22945-5 |
More Info
|
CP 547,632 |
A potent inhibitor of VEGFR2 and bFGF (IC50s = 11 and 9 nM, respectively);… |
1 mg |
21773-1 |
More Info
|
CP 547,632 |
A potent inhibitor of VEGFR2 and bFGF (IC50s = 11 and 9 nM, respectively);… |
5 mg |
21773-5 |
More Info
|
CP 547,632 |
A potent inhibitor of VEGFR2 and bFGF (IC50s = 11 and 9 nM, respectively);… |
500 µg |
21773-500 |
More Info
|
CP 640,186 |
An ACC inhibitor (IC50s = 53 and 61 nM for rat liver ACC1 and rat skeletal… |
1 mg |
17691-1 |
More Info
|
CP 640,186 |
An ACC inhibitor (IC50s = 53 and 61 nM for rat liver ACC1 and rat skeletal… |
10 mg |
17691-10 |
More Info
|
CP 640,186 |
An ACC inhibitor (IC50s = 53 and 61 nM for rat liver ACC1 and rat skeletal… |
25 mg |
17691-25 |
More Info
|
CP 640,186 |
An ACC inhibitor (IC50s = 53 and 61 nM for rat liver ACC1 and rat skeletal… |
5 mg |
17691-5 |
More Info
|
CP 671,305 |
A potent PDE4D inhibitor (IC50 = 3 nM); selective for PDE4D over PDE4A, -B… |
1 mg |
26743-1 |
More Info
|
CP 671,305 |
A potent PDE4D inhibitor (IC50 = 3 nM); selective for PDE4D over PDE4A, -B… |
10 mg |
26743-10 |
More Info
|
CP 671,305 |
A potent PDE4D inhibitor (IC50 = 3 nM); selective for PDE4D over PDE4A, -B… |
5 mg |
26743-5 |
More Info
|
CP 673,451 |
A selective inhibitor of PDGFRβ and PDGFRα kinases (IC50s = 1 a… |
1 mg |
19170-1 |
More Info
|
CP 673,451 |
A selective inhibitor of PDGFRβ and PDGFRα kinases (IC50s = 1 a… |
10 mg |
19170-10 |
More Info
|
CP 673,451 |
A selective inhibitor of PDGFRβ and PDGFRα kinases (IC50s = 1 a… |
5 mg |
19170-5 |
More Info
|
CP 724,714 |
A selective inhibitor of HER2 / ErbB2 (IC50 = 10 nM); inhibits the prolife… |
1 mg |
19172-1 |
More Info
|
CP 724,714 |
A selective inhibitor of HER2 / ErbB2 (IC50 = 10 nM); inhibits the prolife… |
10 mg |
19172-10 |
More Info
|
CP 724,714 |
A selective inhibitor of HER2 / ErbB2 (IC50 = 10 nM); inhibits the prolife… |
25 mg |
19172-25 |
More Info
|
CP 724,714 |
A selective inhibitor of HER2 / ErbB2 (IC50 = 10 nM); inhibits the prolife… |
5 mg |
19172-5 |
More Info
|
CP 775,146 |
A PPARα agonist; binds selectively to PPARα (Ki = 24.5 nM) ove… |
1 mg |
28290-1 |
More Info
|
CP 775,146 |
A PPARα agonist; binds selectively to PPARα (Ki = 24.5 nM) ove… |
10 mg |
28290-10 |
More Info
|
CP 775,146 |
A PPARα agonist; binds selectively to PPARα (Ki = 24.5 nM) ove… |
25 mg |
28290-25 |
More Info
|
CP 775,146 |
A PPARα agonist; binds selectively to PPARα (Ki = 24.5 nM) ove… |
5 mg |
28290-5 |
More Info
|
CP 80,633 |
A selective inhibitor of PDE4 (IC50 = 1.27 µM for PDE4 versus >100 &… |
1 mg |
13183-1 |
More Info
|
CP 80,633 |
A selective inhibitor of PDE4 (IC50 = 1.27 µM for PDE4 versus >100 &… |
10 mg |
13183-10 |
More Info
|
CP 80,633 |
A selective inhibitor of PDE4 (IC50 = 1.27 µM for PDE4 versus >100 &… |
5 mg |
13183-5 |
More Info
|
CP 80,633 |
A selective inhibitor of PDE4 (IC50 = 1.27 µM for PDE4 versus >100 &… |
500 µg |
13183-500 |
More Info
|
CP 809,101 |
A potent 5-HT2C receptor agonist (Ki = 1.6 nM); selective for human 5-HT2C… |
10 mg |
24214-10 |
More Info
|
CP 809,101 |
A potent 5-HT2C receptor agonist (Ki = 1.6 nM); selective for human 5-HT2C… |
25 mg |
24214-25 |
More Info
|
CP 809,101 |
A potent 5-HT2C receptor agonist (Ki = 1.6 nM); selective for human 5-HT2C… |
5 mg |
24214-5 |
More Info
|
CP 809,101 |
A potent 5-HT2C receptor agonist (Ki = 1.6 nM); selective for human 5-HT2C… |
50 mg |
24214-50 |
More Info
|
CP 91,149 |
An inhibitor of LGPa, MGPa, and MGPb (IC50s = 0.13, 0.2, and 0.3 µM,… |
10 mg |
17709-10 |
More Info
|
CP 91,149 |
An inhibitor of LGPa, MGPa, and MGPb (IC50s = 0.13, 0.2, and 0.3 µM,… |
25 mg |
17709-25 |
More Info
|
CP 91,149 |
An inhibitor of LGPa, MGPa, and MGPb (IC50s = 0.13, 0.2, and 0.3 µM,… |
5 mg |
17709-5 |
More Info
|
CP102 |
An iron chelator; decreases hepatic total non-heme and ferritin-stored iro… |
1 mg |
33324-1 |
More Info
|
CP102 |
An iron chelator; decreases hepatic total non-heme and ferritin-stored iro… |
10 mg |
33324-10 |
More Info
|
CP102 |
An iron chelator; decreases hepatic total non-heme and ferritin-stored iro… |
5 mg |
33324-5 |
More Info
|
CP21 |
An iron chelator; active against P. falciparum at 10 and 100 µM; inh… |
1 mg |
33318-1 |
More Info
|
CP21 |
An iron chelator; active against P. falciparum at 10 and 100 µM; inh… |
10 mg |
33318-10 |
More Info
|
CP21 |
An iron chelator; active against P. falciparum at 10 and 100 µM; inh… |
25 mg |
33318-25 |
More Info
|
CP21 |
An iron chelator; active against P. falciparum at 10 and 100 µM; inh… |
5 mg |
33318-5 |
More Info
|
CP94 |
An iron chelator; enhances protoporphyrin IX photobleaching and decreases… |
1 mg |
33323-1 |
More Info
|
CP94 |
An iron chelator; enhances protoporphyrin IX photobleaching and decreases… |
10 mg |
33323-10 |
More Info
|