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D-erythro-Sphingosine hydrochloride , CAS No.2673-72-5

In stock
Item Number
D651899
Grouped product items
SKU Size
Availability
Price Qty
D651899-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$80.90
D651899-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$140.90

Basic Description

Biochemical and Physiological Mechanisms D-erythro-Sphingosine (Erythrosphingosine) hydrochloride is a specific TRPM3 activator. D-erythro-Sphingosine also induces retinoblastoma protein dephosphorylation.
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
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Product Description

D-erythro-Sphingosine (Erythrosphingosine) hydrochloride is a specific TRPM3 activator. D-erythro-Sphingosine also induces retinoblastoma protein dephosphorylation

In Vitro

Extracellular application of D-erythro-Sphingosine (20 μM) induces an increase in [Ca 2+ ] i in TRPM3-transfected HEK293 cells within 20 to 30 s after start of application, whereas nontransfected control cells (NT) shows only very small responses. D-erythro-Sphingosine (10 μM) induces currents through TRPM3. Induction of retinoblastoma protein dephosphorylation by D-erythro-Sphingosine (500 nM; 24 h) precede inhibition of growth and a specific arrest in the G0/G1 phase of the cell cycle. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

IC50& Target:TRPM3|Retinoblastoma protein

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic nitrogen compounds
Class Organonitrogen compounds
Subclass Amines
Intermediate Tree Nodes Alkanolamines
Direct Parent 1,2-aminoalcohols
Alternative Parents Secondary alcohols  Primary alcohols  Monoalkylamines  Hydrochlorides  Hydrocarbon derivatives  
Molecular Framework Aliphatic acyclic compounds
Substituents Secondary alcohol - 1,2-aminoalcohol - Organic oxygen compound - Hydrocarbon derivative - Hydrochloride - Primary amine - Primary alcohol - Organooxygen compound - Primary aliphatic amine - Alcohol - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as 1,2-aminoalcohols. These are organic compounds containing an alkyl chain with an amine group bound to the C1 atom and an alcohol group bound to the C2 atom.
External Descriptors Not available

Names and Identifiers

IUPAC Name (E,2S,3R)-2-aminooctadec-4-ene-1,3-diol;hydrochloride
INCHI InChI=1S/C18H37NO2.ClH/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;1H/b15-14+;/t17-,18+;/m0./s1
InChIKey YDIHJJLAPMAISR-ZNWYJMOFSA-N
Smiles CCCCCCCCCCCCCC=CC(C(CO)N)O.Cl
Isomeric SMILES CCCCCCCCCCCCC/C=C/[C@H]([C@H](CO)N)O.Cl
PubChem CID 17998971
Molecular Weight 336

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Molecular Weight 336.000 g/mol
XLogP3
Hydrogen Bond Donor Count 4
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 15
Exact Mass 335.259 Da
Monoisotopic Mass 335.259 Da
Topological Polar Surface Area 66.500 Ų
Heavy Atom Count 22
Formal Charge 0
Complexity 231.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 2
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 1
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 1
Covalently-Bonded Unit Count 2

Solution Calculators

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