Aristolochic Acid D |
An alkaloid |
10 mg |
35492-10 |
More Info
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Aristolochic Acid D |
An alkaloid |
5 mg |
35492-5 |
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Aristolone |
A sesquiterpene with anticancer activity; cytotoxic to H460, ES-2, and DU1… |
10 mg |
36157-10 |
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Aristolone |
A sesquiterpene with anticancer activity; cytotoxic to H460, ES-2, and DU1… |
25 mg |
36157-25 |
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Aristolone |
A sesquiterpene with anticancer activity; cytotoxic to H460, ES-2, and DU1… |
5 mg |
36157-5 |
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Aristolone |
A sesquiterpene with anticancer activity; cytotoxic to H460, ES-2, and DU1… |
50 mg |
36157-50 |
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Arjunolic Acid |
A triterpene; scavenges DPPH radicals in a cell-free assay at 0.8 mM; prev… |
1 mg |
29438-1 |
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Arjunolic Acid |
A triterpene; scavenges DPPH radicals in a cell-free assay at 0.8 mM; prev… |
10 mg |
29438-10 |
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Arjunolic Acid |
A triterpene; scavenges DPPH radicals in a cell-free assay at 0.8 mM; prev… |
5 mg |
29438-5 |
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Arjunolic Acid |
A triterpene; scavenges DPPH radicals in a cell-free assay at 0.8 mM; prev… |
500 µg |
29438-500 |
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ARM1 |
A thiazolamine that inhibits LTB4 synthesis in human neutrophils (IC50 = ~… |
10 mg |
15865-10 |
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ARM1 |
A thiazolamine that inhibits LTB4 synthesis in human neutrophils (IC50 = ~… |
100 mg |
15865-100 |
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ARM1 |
A thiazolamine that inhibits LTB4 synthesis in human neutrophils (IC50 = ~… |
5 mg |
15865-5 |
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ARM1 |
A thiazolamine that inhibits LTB4 synthesis in human neutrophils (IC50 = ~… |
50 mg |
15865-50 |
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ARN1203 |
A fluorinated analog of AEA that serves as a substrate of FAAH (Km = 29 &m… |
1 mg |
16065-1 |
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ARN1203 |
A fluorinated analog of AEA that serves as a substrate of FAAH (Km = 29 &m… |
10 mg |
16065-10 |
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ARN1203 |
A fluorinated analog of AEA that serves as a substrate of FAAH (Km = 29 &m… |
5 mg |
16065-5 |
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ARN1203 |
A fluorinated analog of AEA that serves as a substrate of FAAH (Km = 29 &m… |
500 µg |
16065-500 |
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ARN14686 |
An affinity probe for NAAA using click chemistry; inhibits the hydrolysis… |
1 mg |
24261-1 |
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ARN14686 |
An affinity probe for NAAA using click chemistry; inhibits the hydrolysis… |
10 mg |
24261-10 |
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ARN14686 |
An affinity probe for NAAA using click chemistry; inhibits the hydrolysis… |
25 mg |
24261-25 |
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ARN14686 |
An affinity probe for NAAA using click chemistry; inhibits the hydrolysis… |
5 mg |
24261-5 |
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ARN14974 |
An inhibitor of acid ceramidase (IC50 = 79 nM); inhibits acid ceramidase a… |
1 mg |
17119-1 |
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ARN14974 |
An inhibitor of acid ceramidase (IC50 = 79 nM); inhibits acid ceramidase a… |
10 mg |
17119-10 |
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ARN14974 |
An inhibitor of acid ceramidase (IC50 = 79 nM); inhibits acid ceramidase a… |
25 mg |
17119-25 |
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ARN14974 |
An inhibitor of acid ceramidase (IC50 = 79 nM); inhibits acid ceramidase a… |
5 mg |
17119-5 |
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ARN14988 |
A potent inhibitor of acid ceramidase (IC50 = 12.8 nM for the human enzyme… |
1 mg |
24284-1 |
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ARN14988 |
A potent inhibitor of acid ceramidase (IC50 = 12.8 nM for the human enzyme… |
10 mg |
24284-10 |
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ARN14988 |
A potent inhibitor of acid ceramidase (IC50 = 12.8 nM for the human enzyme… |
25 mg |
24284-25 |
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ARN14988 |
A potent inhibitor of acid ceramidase (IC50 = 12.8 nM for the human enzyme… |
5 mg |
24284-5 |
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ARN19874 |
An inhibitor of NAPE-PLD (IC50 = 33.7 µM); selective for NAPD-PLD ov… |
1 mg |
24283-1 |
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ARN19874 |
An inhibitor of NAPE-PLD (IC50 = 33.7 µM); selective for NAPD-PLD ov… |
10 mg |
24283-10 |
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ARN19874 |
An inhibitor of NAPE-PLD (IC50 = 33.7 µM); selective for NAPD-PLD ov… |
5 mg |
24283-5 |
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ARN19874 |
An inhibitor of NAPE-PLD (IC50 = 33.7 µM); selective for NAPD-PLD ov… |
500 µg |
24283-500 |
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ARN24139 |
A topoisomerase II poison (IC50 = 7.3 µM); inhibits proliferation of… |
1 mg |
31062-1 |
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ARN24139 |
A topoisomerase II poison (IC50 = 7.3 µM); inhibits proliferation of… |
10 mg |
31062-10 |
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ARN24139 |
A topoisomerase II poison (IC50 = 7.3 µM); inhibits proliferation of… |
5 mg |
31062-5 |
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ARN3236 |
An inhibitor of SIK2 (IC50 = 50s = 21.63 and 6.63 nM, respectively); inhib… |
1 mg |
31457-1 |
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ARN3236 |
An inhibitor of SIK2 (IC50 = 50s = 21.63 and 6.63 nM, respectively); inhib… |
10 mg |
31457-10 |
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ARN3236 |
An inhibitor of SIK2 (IC50 = 50s = 21.63 and 6.63 nM, respectively); inhib… |
25 mg |
31457-25 |
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ARN3236 |
An inhibitor of SIK2 (IC50 = 50s = 21.63 and 6.63 nM, respectively); inhib… |
5 mg |
31457-5 |
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ARN-509 |
An orally bioavailable antagonist of the androgen receptor (IC50 = 16 nM);… |
1 mg |
17132-1 |
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ARN-509 |
An orally bioavailable antagonist of the androgen receptor (IC50 = 16 nM);… |
10 mg |
17132-10 |
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ARN-509 |
An orally bioavailable antagonist of the androgen receptor (IC50 = 16 nM);… |
5 mg |
17132-5 |
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ARN726 |
An NAAA inhibitor (IC50s = 27 and 63 nM for the human and rat enzyme, resp… |
1 mg |
24259-1 |
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ARN726 |
An NAAA inhibitor (IC50s = 27 and 63 nM for the human and rat enzyme, resp… |
10 mg |
24259-10 |
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ARN726 |
An NAAA inhibitor (IC50s = 27 and 63 nM for the human and rat enzyme, resp… |
25 mg |
24259-25 |
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ARN726 |
An NAAA inhibitor (IC50s = 27 and 63 nM for the human and rat enzyme, resp… |
5 mg |
24259-5 |
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ARN810 |
A SERD; binds to ERα and ERβ (IC50s = 6.1 and 8.8 nM, respectiv… |
1 mg |
29595-1 |
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ARN810 |
A SERD; binds to ERα and ERβ (IC50s = 6.1 and 8.8 nM, respectiv… |
10 mg |
29595-10 |
More Info
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