ID: ALA5202564

Max Phase: Preclinical

Molecular Formula: C18H18O4

Molecular Weight: 298.34

Associated Items:

Representations

Canonical SMILES:  Cc1cc(CO)cc2ccc(CO)c(/C=C\C=C\C(=O)O)c12

Standard InChI:  InChI=1S/C18H18O4/c1-12-8-13(10-19)9-14-6-7-15(11-20)16(18(12)14)4-2-3-5-17(21)22/h2-9,19-20H,10-11H2,1H3,(H,21,22)/b4-2-,5-3+

Standard InChI Key:  SQRNZIGOQXVHCN-VOERYJCWSA-N

Associated Targets(non-human)

Aeromonas hydrophila 292 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Edwardsiella tarda 165 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Micrococcus luteus 7463 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pseudomonas aeruginosa 123386 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Vibrio anguillarum 183 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Vibrio alginolyticus 165 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Vibrio parahaemolyticus 473 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Alternaria solani 773 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Colletotrichum gloeosporioides 560 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fusarium graminearum 1554 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fusarium oxysporum 3998 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Gaeumannomyces graminis 93 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ceratobasidium cereale 139 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Valsa mali 129 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: 298.34Molecular Weight (Monoisotopic): 298.1205AlogP: 2.79#Rotatable Bonds: 5
Polar Surface Area: 77.76Molecular Species: ACIDHBA: 3HBD: 3
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.51CX Basic pKa: CX LogP: 2.63CX LogD: -0.17
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.59Np Likeness Score: 1.01

References

1. Hu XY, Li XM, Wang BG, Meng LH..  (2022)  Tanzawaic Acid Derivatives: Fungal Polyketides from the Deep-Sea Coral-Derived Endozoic Penicillium steckii AS-324.,  85  (5.0): [PMID:35576457] [10.1021/acs.jnatprod.2c00211]

Source