ID: ALA4635650

Max Phase: Preclinical

Molecular Formula: C20H23ClO6

Molecular Weight: 394.85

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C[C@@H]1C/C=C/CC/C=C/[C@@H](O)CC(=O)Cc2c(Cl)c(O)cc(O)c2C(=O)O1

Standard InChI:  InChI=1S/C20H23ClO6/c1-12-7-5-3-2-4-6-8-13(22)9-14(23)10-15-18(20(26)27-12)16(24)11-17(25)19(15)21/h3,5-6,8,11-13,22,24-25H,2,4,7,9-10H2,1H3/b5-3+,8-6+/t12-,13-/m1/s1

Standard InChI Key:  TUWXCBZAZLTDAW-INELGWBUSA-N

Associated Targets(Human)

A549 127892 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

769-P 491 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HCT-116 91556 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

B-cell line 200 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

Properties

Molecular Weight: 394.85Molecular Weight (Monoisotopic): 394.1183AlogP: 3.46#Rotatable Bonds: 0
Polar Surface Area: 104.06Molecular Species: NEUTRALHBA: 6HBD: 3
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.02CX Basic pKa: CX LogP: 4.35CX LogD: 3.83
Aromatic Rings: 1Heavy Atoms: 27QED Weighted: 0.46Np Likeness Score: 1.96

References

1. Zhou J, Gao Y, Chang JL, Yu HY, Chen J, Zhou M, Meng XG, Ruan HL..  (2020)  Resorcylic Acid Lactones from an Ilyonectria sp.,  83  (5): [PMID:32323537] [10.1021/acs.jnatprod.9b01167]

Source