ID: ALA5198043

Max Phase: Preclinical

Molecular Formula: C15H13Cl2NO3

Molecular Weight: 326.18

Associated Items:

Representations

Canonical SMILES:  CC1=CC(=O)[C@@](C)(O)C(=O)/C1=C\Nc1ccc(Cl)cc1Cl

Standard InChI:  InChI=1S/C15H13Cl2NO3/c1-8-5-13(19)15(2,21)14(20)10(8)7-18-12-4-3-9(16)6-11(12)17/h3-7,18,21H,1-2H3/b10-7-/t15-/m1/s1

Standard InChI Key:  ROGWXVUJMDEFHH-YYRKOSNBSA-N

Associated Targets(non-human)

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Proteus 150 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bacillus cereus 7522 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mycolicibacterium phlei 631 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bacillus subtilis 32866 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Edwardsiella tarda 165 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Acinetobacter baumannii 41033 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: 326.18Molecular Weight (Monoisotopic): 325.0272AlogP: 3.14#Rotatable Bonds: 2
Polar Surface Area: 66.40Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.52CX Basic pKa: CX LogP: 3.28CX LogD: 3.28
Aromatic Rings: 1Heavy Atoms: 21QED Weighted: 0.65Np Likeness Score: -0.11

References

1. Zhang Z, He X, Zhang X, Li D, Wu G, Liu Z, Niu C, Yang L, Song W, Li Z, Wang Z..  (2022)  Production of Multiple Talaroenamines from Penicillium malacosphaerulum via One-Pot/Two-Stage Precursor-Directed Biosynthesis.,  85  (9.0): [PMID:35993848] [10.1021/acs.jnatprod.2c00394]

Source