Drug Information
Drug General Information | |||||
---|---|---|---|---|---|
Drug ID |
D0J1KH
|
||||
Former ID |
DNC007961
|
||||
Drug Name |
NSC-95397
|
||||
Drug Type |
Small molecular drug
|
||||
Indication | Discovery agent | Investigative | [529691] | ||
Structure |
Download2D MOL |
||||
Formula |
C14H14O4S2
|
||||
Canonical SMILES |
C1=CC=C2C(=C1)C(=O)C(=C(C2=O)SCCO)SCCO
|
||||
InChI |
1S/C14H14O4S2/c15-5-7-19-13-11(17)9-3-1-2-4-10(9)12(18)14(13)20-8-6-16/h1-4,15-16H,5-8H2
|
||||
InChIKey |
MAASHDQFQDDECQ-UHFFFAOYSA-N
|
||||
PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | M-phase inducer phosphatase 2 | Target Info | Inhibitor | [529691] | |
M-phase inducer phosphatase 1 | Target Info | Inhibitor | [530189] | ||
Reactome | Cyclin B2 mediated events | ||||
Cyclin A/B1 associated events during G2/M transition | |||||
Cyclin A:Cdk2-associated events at S phase entryR-HSA-113510:E2F mediated regulation of DNA replication | |||||
G0 and Early G1 | |||||
Polo-like kinase mediated events | |||||
Activation of ATR in response to replication stress | |||||
Cyclin E associated events during G1/S transition | |||||
G1/S-Specific Transcription | |||||
Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | |||||
Cyclin A:Cdk2-associated events at S phase entry | |||||
WikiPathways | Senescence and Autophagy in Cancer | ||||
MAPK Signaling Pathway | |||||
Retinoblastoma (RB) in Cancer | |||||
Prostate Cancer | |||||
Integrated Breast Cancer Pathway | |||||
Integrated Cancer pathway | |||||
Mitotic G2-G2/M phases | |||||
Cell CycleWP707:DNA Damage Response | |||||
G1 to S cell cycle control | |||||
S Phase | |||||
ATM Signaling Pathway | |||||
Mitotic G1-G1/S phases | |||||
Cell Cycle | |||||
Cell Cycle Checkpoints | |||||
miRNAs involved in DNA damage response | |||||
miRNA Regulation of DNA Damage Response | |||||
References | |||||
Ref 529691 | Bioorg Med Chem. 2008 Oct 1;16(19):9040-9. Epub 2008 Aug 7.Novel naphthoquinone and quinolinedione inhibitors of CDC25 phosphatase activity with antiproliferative properties. | ||||
Ref 530189 | Bioorg Med Chem Lett. 2009 Aug 1;19(15):4330-4. Epub 2009 May 27.Structure-based de novo design and biochemical evaluation of novel Cdc25 phosphatase inhibitors. |
If You Find Any Error in Data or Bug in Web Service, Please Kindly Report It to Dr. Zhou and Dr. Zhang.