(S)-((S)-7-methyl-6,8-dioxo-3-(penta-1,3-dienyl)-7,8-dihydro-6H-isochromen-7-yl)2-hydroxypropanoate

ID: ALA2251564

Chembl Id: CHEMBL2251564

PubChem CID: 76326344

Max Phase: Preclinical

Molecular Formula: C18H18O6

Molecular Weight: 330.34

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  C/C=C/C=C/C1=CC2=CC(=O)[C@](C)(OC(=O)[C@H](C)O)C(=O)C2=CO1

Standard InChI:  InChI=1S/C18H18O6/c1-4-5-6-7-13-8-12-9-15(20)18(3,24-17(22)11(2)19)16(21)14(12)10-23-13/h4-11,19H,1-3H3/b5-4+,7-6+/t11-,18-/m0/s1

Standard InChI Key:  GNGQSOUPKHXNOE-BBKFSIMHSA-N

Alternative Forms

  1. Parent:

    ALA2251564

    T22AZAPHILONE

Associated Targets(non-human)

Plenodomus lingam (178 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Botrytis cinerea (4183 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Phytophthora cinnamomi (17 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Globisporangium ultimum (223 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rhizoctonia solani (2251 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Gaeumannomyces tritici (238 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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

Calculated Properties

Molecular Weight: 330.34Molecular Weight (Monoisotopic): 330.1103AlogP: 1.68#Rotatable Bonds: 4
Polar Surface Area: 89.90Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 12.99CX Basic pKa: CX LogP: 1.85CX LogD: 1.85
Aromatic Rings: Heavy Atoms: 24QED Weighted: 0.48Np Likeness Score: 2.63

References

1. Vinale F, Ghisalberti EL, Sivasithamparam K, Marra R, Ritieni A, Ferracane R, Woo S, Lorito M..  (2009)  Factors affecting the production of Trichoderma harzianum secondary metabolites during the interaction with different plant pathogens.,  48  (6): [PMID:19413806] [10.1111/j.1472-765x.2009.02599.x]
2. Vinale F, Marra R, Scala F, Ghisalberti EL, Lorito M, Sivasithamparam K..  (2006)  Major secondary metabolites produced by two commercial Trichoderma strains active against different phytopathogens.,  43  (2): [PMID:16869896] [10.1111/j.1472-765x.2006.01939.x]

Source