ID: ALA4636544

Max Phase: Preclinical

Molecular Formula: C18H19ClO6

Molecular Weight: 366.80

Molecule Type: Unknown

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C18H19ClO6/c1-10-7-11(20)5-3-2-4-6-12(21)8-13-16(18(24)25-10)14(22)9-15(23)17(13)19/h4,6,9-10,22-23H,2-3,5,7-8H2,1H3/b6-4+/t10-/m1/s1

Standard InChI Key:  LJFMEBYJLVOAPT-DFVUYQKZSA-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: 366.80Molecular Weight (Monoisotopic): 366.0870AlogP: 3.11#Rotatable Bonds: 0
Polar Surface Area: 100.90Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.02CX Basic pKa: CX LogP: 4.23CX LogD: 3.71
Aromatic Rings: 1Heavy Atoms: 25QED Weighted: 0.68Np Likeness Score: 1.90

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