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Molecule
ID:90871
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₂₀H₃₉NO₃
Molecular Mass
341.52856
Exact Mass
341.29299411
Charge
0
InChI
InChI=1S/C20H39NO3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-20(24)19(17-22)21-18(2)23/h15-16,19-20,22,24H,3-14,17H2,1-2H3,(H,21,23)/b16-15+/t19-,20+/m0/s1
InChIKey
BLTCBVOJNNKFKC-QUDYQQOWSA-N
Canonic Smiles
CCCCCCCCCCCCC/C=C/[C@H]([C@@H](NC(=O)C)CO)O
Isomeric Smiles
O=C(N[C@H]([C@H](O)/C=C/CCCCCCCCCCCCC)CO)C
Calculated Properties
JChem
LogD (pH = 7.4)
4.39
LogD (pH = 5.5)
4.39
Log P
4.39
Rotatable Bonds
16
H Donor
3
H Acceptors
3
Lipinski's Rule of Five
true
Acid pKa
13.59
Polar Surface Area
69.56
Polarizability
43.32
Molar Refractivity
101.34
LOG S
-6.99
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
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
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RDKit
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JChem
Data Source
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Academic Data
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Commercial Catalog
Names and Identifiers
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Synonyms
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IUPAC Traditional name
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IUPAC name
Registration numbers
Properties
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Product Information
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Physical Property
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Safety Information
Related Proteins
Molecular Spectra
Molecule Details
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TRC
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Apollo Scientific
•
ChEBI
References
•
PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Academic Data
PubChem
5497136
ChEBI
CHEBI:46979
Commercial Catalog
TRC
C262500
Apollo Scientific
OR6251T
Names and Identifiers
Synonyms
C2 Ceeramide
N-[(1S,2R,3E)-2-Hydroxy-1-(hydroxymethyl)-3-heptadecen-1-yl]acetamide
C2 Ceramide
N-Acetyl-D-sphingosine
Acetyl Ceramide
N-Acetylsphingosine
N-acetoyl-D-erythro-sphingosine
N-[(2S,3R)-1,3-dihydroxyoctadec-4-en-2-yl]acetamide
N-acetylsphingosine
C2-ceramide
(2S,3R,4E)-2-(acetylamino)-4-octadecene-1,3-diol
N-(acetyl)-sphing-4-enine
N-acetyl-D-erythro-sphingosine
IUPAC Traditional name
C2-ceramide
IUPAC name
N-[(2S,3R,4E)-1,3-dihydroxyoctadec-4-en-2-yl]acetamide
Registration numbers
MDL Number
MFCD00153903
CAS Number
3102-57-6
PubChem SID
162077580
29214928
PubChem CID
5497136
BRENDA Ligand Database
23510
21320
63299
33123
148258
118927
62892
137789
35168
241234
149369
128952
CHEMBL
CHEMBL105867
UniProt Database
Q8K4Q7
P83006
Q8TCT0
Q9WTY1
Rhea Database
RHEA:58484
RHEA:38755
RHEA:57120
RHEA:38831
RHEA:57108
RHEA:38843
RHEA:38819
RHEA:44512
RHEA:38775
RHEA:44508
RHEA:57136
RHEA:38795
RHEA:57140
RHEA:38799
RHEA:38759
RHEA:62508
RHEA:38771
RHEA:38811
RHEA:62472
RHEA:57116
RHEA:57148
RHEA:38703
RHEA:38791
RHEA:38815
RHEA:47904
RHEA:44536
RHEA:57112
RHEA:38803
RHEA:38835
RHEA:38767
RHEA:44532
RHEA:38763
RHEA:57144
RHEA:38823
RHEA:38839
RHEA:41408
RHEA:38807
RHEA:38827
SwissLipids Database Link
SLM:000001066
BKMS React Database
149369
63299
21320
62892
128952
137789
148258
241234
33123
118927
23510
35168
MetaboLights Database
MTBLS440
MTBLS804
MTBLS670
MTBLS406
SABIO-RK Database
10306
15875
BRENDA Database
3.1.4.4
2.7.8.5
2.7.7.15
2.7.11.24
2.7.1.138
3.4.21.109
3.5.1.23
1.1.1.146
3.1.3.16
CHEBI ID
CHEBI:46979
ACToR Database
3102-57-6
195194-58-2
SureChEMBL Database
SCHEMBL1191825
PubMed Citation Links
27043542
28288862
25656578
28572944
27807662
Reaxys Registry
1728870
Properties
Product Information
Certificate of Analysis
Download link
Source
Physical Property
Apperance
White Solid
Source
Solubility
Chloroform
Source
Dichloromethane
Source
Melting Point
87-89°C
Source
Safety Information
MSDS Link
Download link
Source
Storage Condition
-20°C Freezer
Source
Molecule Details
TRC
C262500
A biologically active, cell permeable, but nonphysiologic ceramide analog. It inhibits cell proliferation and induces monocytic differentiation of HL-60 cells and induces apoptosis. It stimulates protein phosphatase 2A and activates MAP Kinase2.
Apollo Scientific
OR6251T
A biologically active, cell permeable, non-physiological ceramide analog. It inhibits cell proliferation, induces monocytic differentiation of HL-60 cells & inducesapoptosis.
ChEBI
CHEBI:46979
A N-acylsphingosine that has an acetamido group at position 2.
References
PubChem Literature
From Data Sources
•
Inoue, T., et al.: J. Biol. Chem., 284, 9566 (2009)
•
Rath, G., et al.: Int. J. Biochem. Cell Biol., 41, 1165 (2009)
•
Kang, J., et al.: Bioorg. Med. Chem., 17, 1498 (2009)
Bioactivity
PubChem BioAssay
Registration numbers
•
MDL Number
•
CAS Number
•
PubChem SID
•
PubChem CID
•
BRENDA Ligand Database
•
CHEMBL
•
UniProt Database
•
Rhea Database
•
SwissLipids Database Link
•
BKMS React Database
•
MetaboLights Database
•
SABIO-RK Database
•
BRENDA Database
•
CHEBI ID
•
ACToR Database
•
SureChEMBL Database
•
PubMed Citation Links
•
Reaxys Registry