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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H37NO2
Molecular Weight 299.4919
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of SPHINGOSINE

SMILES

CCCCCCCCCCCCC\C=C\[C@@H](O)[C@@H](N)CO

InChI

InChIKey=WWUZIQQURGPMPG-KRWOKUGFSA-N
InChI=1S/C18H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(21)17(19)16-20/h14-15,17-18,20-21H,2-13,16,19H2,1H3/b15-14+/t17-,18+/m0/s1

HIDE SMILES / InChI

Description

Sphingosine harbors two chiral centers and therefore exhibits four stereoisomers, only one of which, the D-erythro (2S,3R) is known to exist naturally. ERYTHRO-SPHINGOSINE, (±)- is a mixture of two isomers: inactive ERYTHRO-SPHINGOSINE, (+)- and the active ERYTHRO-SPHINGOSINE, (-), also known as D-erythro (2S,3R)-SPHINGOSINE or D-erythro –SPHINGOSINE. It was found, that D-erythro –SPHINGOSINE acts as a potent inhibitor of protein kinase C and of transient receptor potential melastatin 7 (TRPM7). Besides, was shown, that sphingosine may be efficacious against alveolar rhabdomyosarcoma, irrespective of TP53 mutation status. It also could evolve as alternative treatment options for aggressive lymphomas via PKC inhibition, apoptosis, and autophagy.

Approval Year

Unknown
139594
Targets

Targets

Primary TargetPharmacologyConditionPotency
Inhibitor
8297
http://www.uniprot.org/uniprot/W0FXB0
2
Target ID: http://www.uniprot.org/uniprot/W0FXB0
Inhibitor
8297
Transient receptor potential cation channel subfamily M member 7
6
Target ID: Q96QT4
Gene ID: 54822.0
Gene Symbol: TRPM7
Target Organism: Homo sapiens (Human)
Inhibitor
8297
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Basic research
Unknown

Approved Use

Unknown
Primary
Basic research
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Sphingosine and FTY720 are potent inhibitors of the transient receptor potential melastatin 7 (TRPM7) channels.
2013 Mar
Patents

Patents

CN103992985A
2
JP1016708A
2
JP2000026271A
2
JP2000109409A
2
JP2000125887A
2
JP2000191496A
2
JP2000256188A
2
JP2001039859A
3
JP2001057890A
2
JP2001064150A
3
JP2001078712A
2
JP2001158735A
2
JP2001158736A
2
JP2001213858A
2
JP2002243737A
2
JP2002326920A
3
JP2002510320A
4
JP2002533379A
53
JP2002544135A
4
JP2002544218A
14
JP2003171229A
2
JP2003171269A
2
JP2003192525A
2
JP2003221369A
2
JP2003252765A
2
JP2003261794A
2
JP2003321393A
7
JP2004196665A
6
JP2004196666A
4
JP2004231616A
2
JP2004256471A
3
JP2004269374A
2
JP2004331594A
2
JP2005002016A
2
JP2005002017A
2
JP2005002018A
2
JP2005002019A
2
JP2005002020A
2
JP2005002021A
2
JP2005002022A
2
JP2005002023A
2
JP2005023068A
2
JP2005220030A
2
JP2005220031A
2
JP2005295994A
2
JP2005529879A
4
JP2005531285A
2
JP2006028196A
2
JP2006045113A
3
JP2006062968A
2
JP2006257069A
2
JP2006515309A
16

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Exogenous addition of D-erythro-sphingosine inhibited the responses in a concentration-dependent manner in the two cell lines: PC12 and L929. D-erythro-sphingosine significantly inhibited mastoparan-, but not Na3VO4-, stimulated arachidonic acid release in PC12 cells. D-erythro-S1P showed no effect on the responses. Production of prostaglandin F2alpha was suppressed by D-erythro-sphingosine (10 microM) in PC12 cells.
Name Type Language
SPHINGOSINE
MI  
Systematic Name English
4-OCTADECENE-1,3-DIOL, 2-AMINO-, (2S,3R,4E)-
Systematic Name English
(2S,3R)-SPHINGOSINE
Systematic Name English
ERYTHRO-4-SPHINGENINE
Common Name English
D-SPHINGOSINE
Common Name English
(-)-D-ERYTHRO-SPHINGOSINE
Common Name English
(-)-SPHINGOSINE
Systematic Name English
4-OCTADECENE-1,3-DIOL, 2-AMINO-, (E)-D-ERYTHRO-
Common Name English
4-OCTADECENE-1,3-DIOL, 2-AMINO-, (R-(R*,S*-(E)))-
Common Name English
SPHINGENINE
Common Name English
C18-SPHINGOSINE
Common Name English
(4E)-SPHINGENINE
Common Name English
4-TRANS-SPHINGENINE
Common Name English
4-SPHINGENINE
Common Name English
(2S,3R,4E)-2-AMINO-4-OCTADECENE-1,3-DIOL
Systematic Name English
SPHINGOSINE [MI]
Common Name English
Code System Code Type Description
CHEBI
16393
Created by admin on Fri Dec 15 15:24:16 GMT 2023 , Edited by admin on Fri Dec 15 15:24:16 GMT 2023
PRIMARY
EPA CompTox
DTXSID90861763
Created by admin on Fri Dec 15 15:24:16 GMT 2023 , Edited by admin on Fri Dec 15 15:24:16 GMT 2023
PRIMARY
FDA UNII
NGZ37HRE42
Created by admin on Fri Dec 15 15:24:16 GMT 2023 , Edited by admin on Fri Dec 15 15:24:16 GMT 2023
PRIMARY
MESH
D013110
Created by admin on Fri Dec 15 15:24:16 GMT 2023 , Edited by admin on Fri Dec 15 15:24:16 GMT 2023
PRIMARY
WIKIPEDIA
SPHINGOSINE
Created by admin on Fri Dec 15 15:24:16 GMT 2023 , Edited by admin on Fri Dec 15 15:24:16 GMT 2023
PRIMARY
PUBCHEM
5280335
Created by admin on Fri Dec 15 15:24:16 GMT 2023 , Edited by admin on Fri Dec 15 15:24:16 GMT 2023
PRIMARY
CHEBI
26743
Created by admin on Fri Dec 15 15:24:16 GMT 2023 , Edited by admin on Fri Dec 15 15:24:16 GMT 2023
PRIMARY
DRUG BANK
DB03203
Created by admin on Fri Dec 15 15:24:16 GMT 2023 , Edited by admin on Fri Dec 15 15:24:16 GMT 2023
PRIMARY
CAS
123-78-4
Created by admin on Fri Dec 15 15:24:16 GMT 2023 , Edited by admin on Fri Dec 15 15:24:16 GMT 2023
PRIMARY
MERCK INDEX
m10144
Created by admin on Fri Dec 15 15:24:16 GMT 2023 , Edited by admin on Fri Dec 15 15:24:16 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
204-651-3
Created by admin on Fri Dec 15 15:24:16 GMT 2023 , Edited by admin on Fri Dec 15 15:24:16 GMT 2023
PRIMARY
CHEBI
45719
Created by admin on Fri Dec 15 15:24:16 GMT 2023 , Edited by admin on Fri Dec 15 15:24:16 GMT 2023
PRIMARY
SUBSTANCE RECORD
Structure of SPHINGOSINE
NIH
NCATS
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ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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