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LX2931 , CAS No.L611629, Inhibitor of sphingosine-1-phosphate lyase 1

COA

Grade & Purity:

Moligand™

PubChem CID: 136034475

In stock

Item Number

L611629

Grouped product items
SKU	Size	Availability	Price	Qty
L611629-5mg	5mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$300.90
L611629-25mg	25mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$1,200.90

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sphingosine-1-phosphate lyase 1 Inhibitor (2)

Basic Description

Synonyms	LX3305
Specifications & Purity	Moligand™
Grade	Moligand™
Action Type	INHIBITOR
Mechanism of action	Inhibitor of sphingosine-1-phosphate lyase 1

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic oxygen compounds
  - Class Organooxygen compounds
    - Subclass Carbohydrates and carbohydrate conjugates

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Class	Organooxygen compounds
Subclass	Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes	Not available
Direct Parent	Sugar alcohols
Alternative Parents	Monosaccharides Imidazolines Secondary alcohols Propargyl-type 1,3-dipolar organic compounds Polyols Enamines C-nitroso compounds Azacyclic compounds Primary alcohols Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic heteromonocyclic compounds
Substituents	Monosaccharide - Sugar alcohol - 4-imidazoline - Secondary alcohol - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Polyol - Organic nitroso compound - Enamine - C-nitroso compound - Organic oxide - Alcohol - Primary alcohol - Organonitrogen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Aliphatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as sugar alcohols. These are hydrogenated forms of carbohydrate in which the carbonyl group (aldehyde or ketone, reducing sugar) has been reduced to a primary or secondary hydroxyl group.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

SGPL1 Tchem Sphingosine-1-phosphate lyase 1 (1 Activities)

Discover Target: SGPL1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Names and Identifiers

IUPAC Name	(1R,2S,3R)-1-[(2E)-2-(1-nitrosoethylidene)-1,3-dihydroimidazol-4-yl]butane-1,2,3,4-tetrol
INCHI	InChI=1S/C9H15N3O5/c1-4(12-17)9-10-2-5(11-9)7(15)8(16)6(14)3-13/h2,6-8,10-11,13-16H,3H2,1H3/b9-4+/t6-,7-,8-/m1/s1
InChIKey	CGJLPLVZAAEKTK-LIVYHJONSA-N
Smiles	C/C(=c/1\[nH]c(c[nH]1)[C@H]([C@@H]([C@@H](CO)O)O)O)/N=O
PubChem CID	136034475

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