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TargetCytochrome P450 2C19
LigandBDBM597562
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2245904 (CHEMBL5160114)
IC50 5400±n/a nM
Citation Taft, BRYokokawa, FKirrane, TMata, ACHuang, RBlaquiere, NWaldron, GZou, BSimon, OVankadara, SChan, WLDing, MSim, SStraimer, JGuiguemde, ALakshminarayana, SBJain, JPBodenreider, CThompson, CLanshoeft, CShu, WFang, EQumber, JChan, KPei, LChen, YLSchulz, HLim, JAbas, SNAng, XLiu, YAngulo-Barturen, IJiménez-Díaz, MBGamo, FJCrespo-Fernandez, BRosenthal, PJCooper, RATumwebaze, PAguiar, ACCCampo, BCampbell, SWagner, JDiagana, TTSarko, C Discovery and Preclinical Pharmacology of INE963, a Potent and Fast-Acting Blood-Stage Antimalarial with a High Barrier to Resistance and Potential for Single-Dose Cures in Uncomplicated Malaria. J Med Chem65:3798-3813 (2022) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Cytochrome P450 2C19
Name:Cytochrome P450 2C19
Synonyms:(R)-limonene 6-monooxygenase | (S)-limonene 6-monooxygenase | (S)-limonene 7-monooxygenase | CP2CJ_HUMAN | CYP2C19 | CYPIIC17 | CYPIIC19 | Cytochrome P450 2C19 (CYP2C19) | Cytochrome P450 2C19 [I331V] | Cytochrome P450-11A | Cytochrome P450-254C | Fenbendazole monooxygenase (4'-hydroxylating) | Mephenytoin 4-hydroxylase | P450-11A | P450-254C
Type:Enzyme
Mol. Mass.:55935.47
Organism:Homo sapiens (Human)
Description:P33261
Residue:490
Sequence:
MDPFVVLVLCLSCLLLLSIWRQSSGRGKLPPGPTPLPVIGNILQIDIKDVSKSLTNLSKI
YGPVFTLYFGLERMVVLHGYEVVKEALIDLGEEFSGRGHFPLAERANRGFGIVFSNGKRW
KEIRRFSLMTLRNFGMGKRSIEDRVQEEARCLVEELRKTKASPCDPTFILGCAPCNVICS
IIFQKRFDYKDQQFLNLMEKLNENIRIVSTPWIQICNNFPTIIDYFPGTHNKLLKNLAFM
ESDILEKVKEHQESMDINNPRDFIDCFLIKMEKEKQNQQSEFTIENLVITAADLLGAGTE
TTSTTLRYALLLLLKHPEVTAKVQEEIERVIGRNRSPCMQDRGHMPYTDAVVHEVQRYID
LIPTSLPHAVTCDVKFRNYLIPKGTTILTSLTSVLHDNKEFPNPEMFDPRHFLDEGGNFK
KSNYFMPFSAGKRICVGEGLARMELFLFLTFILQNFNLKSLIDPKDLDTTPVVNGFASVP
PFYQLCFIPV
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  Blast E-value cutoff:
BDBM597562
n/a
NameBDBM597562
Synonyms:US11597733, Example 4-0
TypeSmall organic molecule
Emp. Form.C19H26N6O2S
Mol. Mass.402.514
SMILESCOc1nc(ccc1-c1cnc2sc(nn12)N1CCC(O)(CN)CC1)C(C)C
Structure
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