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Molecule
ID:128578
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₂₄H₄₆O₂
Molecular Mass
366.62084
Exact Mass
366.34978071
Charge
0
InChI
InChI=1S/C24H46O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24(25)26/h9-10H,2-8,11-23H2,1H3,(H,25,26)/b10-9-
InChIKey
GWHCXVQVJPWHRF-KTKRTIGZSA-N
Canonic Smiles
CCCCCCCC/C=C\CCCCCCCCCCCCCC(=O)O
Isomeric Smiles
O=C(O)CCCCCCCCCCCCC/C=C\CCCCCCCC
Calculated Properties
JChem
LogD (pH = 7.4)
7.04
LogD (pH = 5.5)
8.80
Log P
9.45
Rotatable Bonds
21
H Donor
1
H Acceptors
2
Lipinski's Rule of Five
false
Acid pKa
4.95
Polar Surface Area
37.30
Polarizability
49.86
Molar Refractivity
115.01
LOG S
-10.38
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
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Molecular Spectra
No Data Available
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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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RDKit
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IUPAC Traditional name
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IUPAC name
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From Data Sources
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Data Source
Academic Data
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Nervonic_acid
PubChem
5281120
ChEBI
CHEBI:44247
Commercial Catalog
Sigma Aldrich
N1514
Names and Identifiers
Synonyms
cis
-15-Tetracosenoic acid
24:1 cis, delta 9 or 24:1 omega 9
Nervonic acid
鲨油酸
神经酸
顺-15-二十四碳烯酸
Nervonic acid
Nervonsaeure
(Z)-15-Tetracosenoic acid
selacholeic acid
(Z)-tetracos-15-enoic acid
(15Z)-tetracosenoic acid
15cis-tetracosenoic acid
cis-Delta(15)-tetracosenoic acid
Nervonic acid
cis-15-tetracosenoic acid
(15Z)-Tetracosenoic acid
IUPAC Traditional name
nervonic acid
IUPAC name
(15Z)-tetracos-15-enoic acid
Registration numbers
Wikipedia Title
Nervonic_acid
CHEMBL
1173379
CHEMBL1173379
KEGG ID
C08323
Chemspider ID
4444565
PubChem CID
5281120
CAS Number
506-37-6
CHEBI ID
44247
CHEBI:7526
CHEBI:44247
CHEBI:44244
Beilstein Number
1728551
PubChem SID
24897496
162222885
26697164
MDL Number
MFCD00010507
BRENDA Ligand Database
10732
208304
84175
171300
55058
MetaboLights Database
MTBLS673
MTBLS804
MTBLS1183
MTBLS1693
MTBLS27
MTBLS2081
MTBLS3628
MTBLS548
MTBLS717
MTBLS1903
MTBLS78
MTBLS1140
MTBLS606
MTBLS615
MTBLS2559
BRENDA Database
4.2.2.5
4.2.2.19
3.1.1.13
3.5.1.23
6.2.1.3
4.2.2.1
3.5.1.99
Patent number
EP1905446
US2003065023
US2008090803
US2008153899
US2004122094
US2004242663
US2005130881
EP1914223
KNApSAcK Database
C00001230
BKMS React Database
10732
84175
208304
55058
171300
Protein Data Bank
5urv
2euk
Reaxys Registry
1728551
PubMed Citation Links
21147856
16394593
12742544
9075193
8072429
ACToR Database
506-37-6
Golm Database
14ac0291-7bc5-4fd0-b616-b308a604d8ba
334d7163-24bf-44b4-a9c7-73e1152b1de5
SABIO-RK Database
13803
SureChEMBL Database
SCHEMBL21103
LIPID MAPS Instance
LMFA01030092
Properties
Physical Property
Melting Point
42–43 °C
Source
42-43 °C(lit.)
Source
Flash Point
230 °F
Source
110 °C
Source
Safety Information
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
German water hazard class
3
Source
Safety Statements
26
Source
European Hazard Symbols
Irritant (Xi)
Source
GHS Signal Word
Warning
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
Storage Temperature
-20°C
Source
Risk Statements
36/37/38
Source
Product Information
Purity
≥99% (capillary GC)
Source
Related Proteins
PDB Bank
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5URV
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2EUK
Molecule Details
Wikipedia
Nervonic_acid
Sigma Aldrich
N1514
包装
Sealed ampule.
ChEBI
CHEBI:44247
A tetracosenoic acid having a cis-double bond at position 15.
References
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Bioactivity
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Beilstein Number
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PubChem SID
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MDL Number
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BRENDA Ligand Database
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MetaboLights Database
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BRENDA Database
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Patent number
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KNApSAcK Database
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BKMS React Database
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Protein Data Bank
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Reaxys Registry
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PubMed Citation Links
•
ACToR Database
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Golm Database
•
SABIO-RK Database
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SureChEMBL Database
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LIPID MAPS Instance