(E)-3-(4-Hydroxy-3-methoxy-phenyl)-acrylic acid adamantan-1-yl ester

ID: ALA3327352

Chembl Id: CHEMBL3327352

PubChem CID: 118712239

Max Phase: Preclinical

Molecular Formula: C20H24O4

Molecular Weight: 328.41

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  COc1cc(/C=C/C(=O)OC23CC4CC(CC(C4)C2)C3)ccc1O

Standard InChI:  InChI=1S/C20H24O4/c1-23-18-9-13(2-4-17(18)21)3-5-19(22)24-20-10-14-6-15(11-20)8-16(7-14)12-20/h2-5,9,14-16,21H,6-8,10-12H2,1H3/b5-3+

Standard InChI Key:  WXHDLEAJIGSBOC-HWKANZROSA-N

Alternative Forms

1. Parent:

   

   ALA3327352

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Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 328.41

Molecular Weight (Monoisotopic): 328.1675

AlogP: 3.93

#Rotatable Bonds: 4

Polar Surface Area: 55.76

Molecular Species: NEUTRAL

HBA: 4

HBD: 1

#RO5 Violations: ┄

HBA (Lipinski): 4

HBD (Lipinski): 1

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: 9.87

CX Basic pKa: ┄

CX LogP: 4.15

CX LogD: 4.14

Aromatic Rings: 1

Heavy Atoms: 24

QED Weighted: 0.67

Np Likeness Score: 0.76

References

1. Chen HZ, Chen YB, Lv YP, Zeng F, Zhang J, Zhou YL, Li HB, Chen LF, Zhou BJ, Gao JR, Xia CN..  (2014)  Synthesis and antitumor activity of feruloyl and caffeoyl derivatives.,  24  (18): [PMID:25160837] [10.1016/j.bmcl.2014.08.024]

Source

Source(1):

• Scientific Literature