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Molecule
ID:84063
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₈H₁₈O₅
Molecular Mass
314.33252
Exact Mass
314.11542368
Charge
0
InChI
InChI=1S/C18H18O5/c1-21-16-10-12(11-17(22-2)18(16)23-3)8-9-15(20)13-6-4-5-7-14(13)19/h4-11,19H,1-3H3
InChIKey
SRSBUHVXNLHWHU-UHFFFAOYSA-N
Canonic Smiles
COc1cc(/C=C/C(=O)c2ccccc2O)cc(c1OC)OC
Isomeric Smiles
O=C(c1c(cccc1)O)/C=C/c1cc(c(c(c1)OC)OC)OC
Calculated Properties
JChem
Acid pKa
8.194424
H Acceptors
5
H Donor
1
LogD (pH = 5.5)
3.7628756
LogD (pH = 7.4)
3.699586
Log P
3.7637463
Molar Refractivity
88.2475
Polarizability
33.494236
Polar Surface Area
64.99
Rotatable Bonds
6
Lipinski's Rule of Five
true
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Related Proteins
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
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IUPAC Traditional name
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR26889
InterBioScreen
STOCK1N-34298
Academic Data
PubChem
5709436
Names and Identifiers
IUPAC name
1-(2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one
(2E)-1-(2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one
Synonyms
1-(2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one
IUPAC Traditional name
1-(2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one
crotaoprostrin
Registration numbers
PubChem CID
5709436
PubChem SID
162071179
MDL Number
MFCD00136246
Properties
Product Information
Classification
Derivatives & analogs of Natural Compounds
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay