Lipoyl-AMP (BioCAD00000013417)
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Metabolite Card
Formula: C18H26N5O8PS2 (535.096)
SMILES: NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OC(=O)CCCCC2CCSS2)[C@@H](O)[C@H]1O
Synonyms [en]
Lipoyl-AMP; [[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphoryl] 5-(dithiolan-3-yl)pentanoate; {[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}({[5-(1,2-dithiolan-3-yl)pentanoyl]oxy})phosphinic acid; 5'-O-{5-(1; Q27124302; 5'-O-[{[5-(1,2-dithiolan-3-yl)pentanoyl]oxy}(hydroxy)phosphoryl]adenosine
Last reviewed on 2024-06-28.
Cite this Page
Lipoyl-AMP. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China.
https://biocad_registry.innovation.ac.cn/s/(-)-arctiin
(retrieved
2026-01-03) (CAD Registry RN: BioCAD00000013417). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
Lipoyl-amp is part of the Protein modification, and Lipoic acid metabolism pathways. It is a substrate for: Lipoyltransferase 1, mitochondrial.
DBLinks
- CAS Registry Number: 4466-48-2
- PubChem CID: 23724672
- ChEBI: 55451
- HMDB: HMDB0059635
- LipidMaps:
- KEGG: C16238
- BioCyc:
- NCBI MeSH:
- Wikipedia:
Other DBLinks
- CAS Registry Number: 4466-48-2
- PubChem: 23724672
- ChEBI: ChEBI:55451
- HMDB: HMDB0059635
- KEGG: C16238
- Coconut NaturalProduct: CNP0083380.1
Class / Ontology
- WishartLab ClassyFire: [Purine ribonucleotides] Purine ribonucleotides
- ChEBI: [CHEBI:55451] lipoyl-AMP
- Coconut NaturalProduct: [Purine nucleos(t)ides] Purine nucleos(t)ides
| ID | EC Number | Name |
|---|---|---|
| KEGG:R07770 | 6.3.1.20 | C00002 + C16241<=>C00013 + C16238 |
| KEGG:R07771 | 6.3.1.20 | C16238 + C16240<=>C16237 + C00020 |
| KEGG:R12450 | C16238 + C22158<=>C15972 + C00020 |
Taxonomy Source
Pathway Synthetic
| pathway id | name |
|---|---|
| PathBank:SMP0000793 | Lipoic Acid Metabolism |
| PathBank:SMP0121070 | Lipoic Acid Metabolism |
| PathBank:SMP0002398 | Lipoic Acid Metabolism |