Compound

a beta-D-xylosyl-(1<->1')-N-acylsphing-4-enine

CHEBI:189068ChEBI

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Structure

2D depiction

Class: Organic compound
Formula: C24H44NO7R
Mass: 458.61 g/mol
Charge: 0
SMILES: *C(=O)N[C@@H](CO[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O)[C@H](O)/C=C/CCCCCCCCCCCCC
Look it up: ChEBI

Identity from ChEBI. Not evidence.

What it touches on the way

Mechanistic reach

3 entities

3 entities reached.

0 reported hops3 assembled from the scaffold

What the reference databases state

Chemical structure

a beta-D-xylosyl-(1<->1')-N-acylsphing-4-enine has the functional parent an N-acylsphing-4-enineCompoundChEBI CHEBI:189068Inferred only

Statements

3 statements

3 statements · 1 reference database · Subject: a beta-D-xylosyl-(1<->1')-N-acylsphing-4-enine · Sources: Rhea

Order

a beta-D-xylosyl-(1<->1')-N-acylsphing-4-enine is a substrate of GBA1ProteinRhea RHEA:70239Inferred only
a beta-D-xylosyl-(1<->1')-N-acylsphing-4-enine is a substrate of GBA3ProteinRhea RHEA:70239Inferred only
a beta-D-xylosyl-(1<->1')-N-acylsphing-4-enine is a substrate of UGCGProteinRhea RHEA:70243Inferred only

Reactions

2 reactions

a beta-D-xylosyl-(1<->1')-N-acylsphing-4-enine+cholesterolcholesteryl 3-beta-D-xyloside+an N-acylsphing-4-enine
Catalysed by GBA1 or GBA3
Reaction pageReversibleBalance undeterminable
Rhea RHEA:70239CC BY 4.0Reference data
UDP-alpha-D-xylose+an N-acylsphing-4-eninea beta-D-xylosyl-(1<->1')-N-acylsphing-4-enine+UDP+hydron
Catalysed by UGCG
Reaction pageLeft to rightBalance undeterminable
Rhea RHEA:70243CC BY 4.0Reference data

Other names

4 names

Resolves to: a beta-D-xylosyl-(1<->1')-N-acylsphing-4-enine

Also called: 1-(beta-D-xylosyl)-ceramide(d18:1(4E))1-(beta-D-xylosyl)-N-acylsphingosine1-(β-D-xylosyl)-ceramide(d18:1(4E))1-(β-D-xylosyl)-N-acylsphingosine