ID: ALA5286488

Max Phase: Preclinical

Molecular Formula: C20H21N3O2S

Molecular Weight: 367.47

Associated Items:

Representations

Canonical SMILES:  O=C(CCc1cc2ccccc2s1)N1CCN(c2ccc(O)cn2)CC1

Standard InChI:  InChI=1S/C20H21N3O2S/c24-16-5-7-19(21-14-16)22-9-11-23(12-10-22)20(25)8-6-17-13-15-3-1-2-4-18(15)26-17/h1-5,7,13-14,24H,6,8-12H2

Standard InChI Key:  MRMZDIDRDSTEAB-UHFFFAOYSA-N

Associated Targets(Human)

ME3 Tbio NADP-dependent malic enzyme, mitochondrial (80 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ME2 Tbio NAD-dependent malic enzyme, mitochondrial (32 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ME1 Tchem NADP-dependent malic enzyme (42 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BXPC-3 (2997 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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

Properties

Molecular Weight: 367.47Molecular Weight (Monoisotopic): 367.1354AlogP: 3.28#Rotatable Bonds: 4
Polar Surface Area: 56.67Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 10.07CX Basic pKa: 6.20CX LogP: 3.52CX LogD: 3.49
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.77Np Likeness Score: -1.72

References

1. Sheth G, Shah SR, Sengupta P, Jarag T, Chimanwala S, Sairam KVVM, Jain V, Talwar R, Dhanave A, Raviya M, Menon S, Trivedi S, Chitturi TR..  (2023)  In the Quest for Potent and Selective Malic Enzyme 3 Inhibitors for the Treatment of Pancreatic Ductal Adenocarcinoma.,  14  (1.0): [PMID:36655126] [10.1021/acsmedchemlett.2c00369]

Source