ID: ALA5269501

Max Phase: Preclinical

Molecular Formula: C20H15N5OS

Molecular Weight: 373.44

Associated Items:

Representations

Canonical SMILES:  O=C1CS/C(=N\c2cc(-c3c[nH]c4ccccc34)nn2-c2ccccc2)N1

Standard InChI:  InChI=1S/C20H15N5OS/c26-19-12-27-20(23-19)22-18-10-17(24-25(18)13-6-2-1-3-7-13)15-11-21-16-9-5-4-8-14(15)16/h1-11,21H,12H2,(H,22,23,26)

Standard InChI Key:  NTGIZUSJRIPDJL-UHFFFAOYSA-N

Associated Targets(Human)

BEAS-2B 690 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

A549 127892 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

SK-MEL-28 48833 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HCT-116 91556 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

B16-F10 4610 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: 373.44Molecular Weight (Monoisotopic): 373.0997AlogP: 3.87#Rotatable Bonds: 3
Polar Surface Area: 75.07Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.57CX Basic pKa: 1.10CX LogP: 4.09CX LogD: 3.87
Aromatic Rings: 4Heavy Atoms: 27QED Weighted: 0.57Np Likeness Score: -0.98

References

1. Soni JP, Chilvery S, Sharma A, Reddy GN, Godugu C, Shankaraiah N..  (2023)  Design, synthesis and in vitro cytotoxicity evaluation of indolo-pyrazoles grafted with thiazolidinone as tubulin polymerization inhibitors.,  14  (3): [PMID:36970141] [10.1039/d2md00442a]

Source