8-Hydroxy-2-imino-N-(2-(trifluoromethyl)phenyl)-2H-chromene-3-carboxamide

ID: ALA4640154

Chembl Id: CHEMBL4640154

PubChem CID: 19573991

Max Phase: Preclinical

Molecular Formula: C17H11F3N2O3

Molecular Weight: 348.28

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  N=c1oc2c(O)cccc2cc1C(=O)Nc1ccccc1C(F)(F)F

Standard InChI:  InChI=1S/C17H11F3N2O3/c18-17(19,20)11-5-1-2-6-12(11)22-16(24)10-8-9-4-3-7-13(23)14(9)25-15(10)21/h1-8,21,23H,(H,22,24)

Standard InChI Key:  CNJDAVIXUMTMCU-UHFFFAOYSA-N

Associated Targets(Human)

AKR1C4 Tchem Aldo-keto reductase family 1 member C4 (224 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AKR1C2 Tchem Aldo-keto reductase family 1 member C2 (639 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AKR1C1 Tchem Aldo-keto reductase family 1 member C1 (475 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AKR1C3 Tchem Aldo-keto-reductase family 1 member C3 (1414 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBR1 Tchem Carbonyl reductase [NADPH] 1 (138 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 348.28Molecular Weight (Monoisotopic): 348.0722AlogP: 3.89#Rotatable Bonds: 2
Polar Surface Area: 86.32Molecular Species: NEUTRALHBA: 4HBD: 3
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: 10.24CX Basic pKa: 3.65CX LogP: 4.04CX LogD: 4.04
Aromatic Rings: 3Heavy Atoms: 25QED Weighted: 0.66Np Likeness Score: -1.00

References

1. Endo S, Oguri H, Segawa J, Kawai M, Hu D, Xia S, Okada T, Irie K, Fujii S, Gouda H, Iguchi K, Matsukawa T, Fujimoto N, Nakayama T, Toyooka N, Matsunaga T, Ikari A..  (2020)  Development of Novel AKR1C3 Inhibitors as New Potential Treatment for Castration-Resistant Prostate Cancer.,  63  (18): [PMID:32847363] [10.1021/acs.jmedchem.0c00939]

Source