(Z)-2-phthalimido-2-butenoic acid

ID: ALA2289109

Chembl Id: CHEMBL2289109

PubChem CID: 76313050

Max Phase: Preclinical

Molecular Formula: C12H9NO4

Molecular Weight: 231.21

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  C/C=C(/C(=O)O)N1C(=O)c2ccccc2C1=O

Standard InChI:  InChI=1S/C12H9NO4/c1-2-9(12(16)17)13-10(14)7-5-3-4-6-8(7)11(13)15/h2-6H,1H3,(H,16,17)/b9-2-

Standard InChI Key:  ONLWHECOPCAXMD-MBXJOHMKSA-N

Alternative Forms

  1. Parent:

Associated Targets(non-human)

Vigna mungo (68 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Brassica rapa subsp. pekinensis (26 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lactuca sativa (1092 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Oryza sativa (2923 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: 231.21Molecular Weight (Monoisotopic): 231.0532AlogP: 1.27#Rotatable Bonds: 2
Polar Surface Area: 74.68Molecular Species: ACIDHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 3.16CX Basic pKa: CX LogP: 1.31CX LogD: -2.15
Aromatic Rings: 1Heavy Atoms: 17QED Weighted: 0.61Np Likeness Score: 0.33

References

1. TANAKA S, KATAYAMA M.  (2000)  Hydrogenated and Dichiorinated N-Phthaloyl-L-threonines and Their Dehydrated Phthalimides with Root Growth-promoting Activity for Rice Seedings,  25  (2): [10.1584/jpestics.25.133]

Source