2-Ethylcarbamoyl-3,7-dimethyl-9-(2,6,6-trimethyl-cyclohex-1-enyl)-nona-2,4,6,8-tetraenoic acid

ID: ALA14287

Chembl Id: CHEMBL14287

PubChem CID: 14058244

Max Phase: Preclinical

Molecular Formula: C23H33NO3

Molecular Weight: 371.52

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCNC(=O)/C(C(=O)O)=C(C)\C=C\C=C(C)\C=C\C1=C(C)CCCC1(C)C

Standard InChI:  InChI=1S/C23H33NO3/c1-7-24-21(25)20(22(26)27)18(4)11-8-10-16(2)13-14-19-17(3)12-9-15-23(19,5)6/h8,10-11,13-14H,7,9,12,15H2,1-6H3,(H,24,25)(H,26,27)/b11-8+,14-13+,16-10+,20-18+

Standard InChI Key:  BOPGZYTZIJQPIR-PPNLBOGDSA-N

Associated Targets(non-human)

F9 (77 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: 371.52Molecular Weight (Monoisotopic): 371.2460AlogP: 5.11#Rotatable Bonds: 7
Polar Surface Area: 66.40Molecular Species: ACIDHBA: 2HBD: 2
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 4.21CX Basic pKa: CX LogP: 4.38CX LogD: 1.35
Aromatic Rings: Heavy Atoms: 27QED Weighted: 0.28Np Likeness Score: 1.47

References

1. Shealy YF, Krauth CA, Riordan JM, Sani BP..  (1988)  Terminal bifunctional retinoids. Synthesis and evaluations related to cancer chemopreventive activity.,  31  (6): [PMID:2836589] [10.1021/jm00401a011]

Source