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Molecule
ID:133173
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₂₁H₃₆O₄
Molecular Mass
352.50814
Exact Mass
352.26135963
Charge
0
InChI
InChI=1S/C21H36O4/c1-8-13(4)18(22)16(7)19(23)14(5)10-12(3)11-15(6)20-17(9-2)21(24)25-20/h10,13-18,20,22H,8-9,11H2,1-7H3/b12-10+/t13-,14-,15+,16+,17+,18-,20+/m1/s1
InChIKey
UNBMQQNYLCPCHS-VYNDPHDASA-N
Canonic Smiles
CC[C@H]([C@H]([C@@H](C(=O)[C@@H](/C=C(/C[C@@H]([C@@H]1OC(=O)[C@H]1CC)C)\C)C)C)O)C
Isomeric Smiles
CC[C@H]1[C@@H](OC1=O)[C@@H](C)C/C(=C/[C@@H](C)C(=O)[C@@H](C)[C@@H]([C@H](C)CC)O)/C
Calculated Properties
JChem
Acid pKa
14.498025
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
5.0759892
LogD (pH = 7.4)
5.0759892
Log P
5.0759892
Molar Refractivity
100.7281
Polarizability
39.892128
Polar Surface Area
63.6
Rotatable Bonds
10
Lipinski's Rule of Five
false
Data Source
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Related Proteins
No Data Available
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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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IUPAC name
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PubChem SID
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MDL Number
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PubChem CID
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Sigma Aldrich
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From Data Sources
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PubChem BioAssay
Data Source
Commercial Catalog
Sigma Aldrich
E0886
Academic Data
PubChem
6436821
Names and Identifiers
Synonyms
Ebelactone B microbial
2-Ethyl-3,11-dihydroxy-4,6,8,10,12-pentamethyl-9-oxo-6-tetradecenoic acid 1,3-lactone
IUPAC Traditional name
(3S,4S)-3-ethyl-4-[(2S,4E,6R,8S,9R,10R)-9-hydroxy-4,6,8,10-tetramethyl-7-oxododec-4-en-2-yl]oxetan-2-one
IUPAC name
(3S,4S)-3-ethyl-4-[(2S,4E,6R,8S,9R,10R)-9-hydroxy-4,6,8,10-tetramethyl-7-oxododec-4-en-2-yl]oxetan-2-one
Registration numbers
CAS Number
76808-15-6
PubChem SID
24894376
162227450
MDL Number
MFCD00036711
PubChem CID
6436821
Properties
Product Information
Purity
≥95% (HPLC)
Source
Safety Information
RTECS
RQ7720000
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Storage Temperature
2-8°C
Source
German water hazard class
3
Source
Molecule Details
Sigma Aldrich
E0886
Biochem/physiol Actions
Esterase (lipase) inhibitor. Also inhibits carboxypeptidase Y-like kininase that degrades bradykinin.1
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay