ID: ALA269929

Max Phase: Preclinical

Molecular Formula: C23H22O3

Molecular Weight: 346.43

Molecule Type: Small molecule

Representations

Canonical SMILES:  C=CCOc1ccc(/C=C/C(=O)/C=C/c2ccc(OCC=C)cc2)cc1

Standard InChI:  InChI=1S/C23H22O3/c1-3-17-25-22-13-7-19(8-14-22)5-11-21(24)12-6-20-9-15-23(16-10-20)26-18-4-2/h3-16H,1-2,17-18H2/b11-5+,12-6+

Standard InChI Key:  HMZANBKZFJOKDD-YDWXAUTNSA-N

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

Properties

Molecular Weight: 346.43

Molecular Weight (Monoisotopic): 346.1569

AlogP: 5.11

#Rotatable Bonds: 10

Polar Surface Area: 35.53

Molecular Species: NEUTRAL

HBA: 3

HBD: 0

#RO5 Violations: 1

HBA (Lipinski): 3

HBD (Lipinski): 0

#RO5 Violations (Lipinski): 1

CX Acidic pKa:

CX Basic pKa:

CX LogP: 5.97

CX LogD: 5.97

Aromatic Rings: 2

Heavy Atoms: 26

QED Weighted: 0.44

Np Likeness Score: 0.06

References

1. Liang G, Li X, Chen L, Yang S, Wu X, Studer E, Gurley E, Hylemon PB, Ye F, Li Y, Zhou H..  (2008)  Synthesis and anti-inflammatory activities of mono-carbonyl analogues of curcumin.,  18  (4): [PMID:18234497] [10.1016/j.bmcl.2007.12.068]

2. Liang G, Shao L, Wang Y, Zhao C, Chu Y, Xiao J, Zhao Y, Li X, Yang S..  (2009)  Exploration and synthesis of curcumin analogues with improved structural stability both in vitro and in vivo as cytotoxic agents.,  17  (6): [PMID:19243951] [10.1016/j.bmc.2008.10.044]

3. Lin H, Hu GX, Guo J, Ge Y, Liang G, Lian QQ, Chu Y, Yuan X, Huang P, Ge RS..  (2013)  Mono-carbonyl curcumin analogues as 11β-hydroxysteroid dehydrogenase 1 inhibitors.,  23  (15): [PMID:23800686] [10.1016/j.bmcl.2013.05.080]

4. Liu Z, Tang L, Zou P, Zhang Y, Wang Z, Fang Q, Jiang L, Chen G, Xu Z, Zhang H, Liang G..  (2014)  Synthesis and biological evaluation of allylated and prenylated mono-carbonyl analogs of curcumin as anti-inflammatory agents.,  74  [PMID:24321865] [10.1016/j.ejmech.2013.10.061]

Source

Source(1):

• Scientific Literature