Target Validation Information | |||||
---|---|---|---|---|---|
TTD ID | T30823 | ||||
Target Name | M-phase inducer phosphatase 1 (MPIP1) | ||||
Type of Target |
Literature-reported |
||||
Drug Potency against Target | (E)-2-(1-decyl-2-oxoindolin-3-ylidene)acetic acid | Drug Info | IC50 = 13000 nM | [2] | |
(Z)-2-(1-decyl-2-oxoindolin-3-ylidene)acetic acid | Drug Info | IC50 = 12000 nM | [2] | ||
1-dodecyl-1H-indole-2,3-dione | Drug Info | IC50 = 15000 nM | [2] | ||
2-(1-dodecyl-1H-indol-3-yl)acetic acid | Drug Info | IC50 = 8000 nM | [2] | ||
3-isopropyl-4-(phenylamino)naphthalene-1,2-dione | Drug Info | IC50 = 10880 nM | [1] | ||
3-isopropyl-4-(phenylthio)naphthalene-1,2-dione | Drug Info | IC50 = 5860 nM | [1] | ||
3-isopropyl-4-phenylnaphthalene-1,2-dione | Drug Info | IC50 = 7830 nM | [1] | ||
3-isopropylnaphthalene-1,2-dione | Drug Info | IC50 = 11180 nM | [1] | ||
4-(p-toluidino)-3-isopropylnaphthalene-1,2-dione | Drug Info | IC50 = 7060 nM | [1] | ||
NSC-95397 | Drug Info | IC50 = 5500 nM | [3] | ||
References | |||||
REF 1 | Synthesis of miltirone analogues as inhibitors of Cdc25 phosphatases. Bioorg Med Chem Lett. 2006 Apr 1;16(7):1905-8. | ||||
REF 2 | Design and synthesis of N-alkyl oxindolylidene acetic acids as a new class of potent Cdc25A inhibitors. Bioorg Med Chem Lett. 2008 Jun 1;18(11):3350-3. | ||||
REF 3 | Structure-based de novo design and biochemical evaluation of novel Cdc25 phosphatase inhibitors. Bioorg Med Chem Lett. 2009 Aug 1;19(15):4330-4. | ||||
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