Cyclo[(2Z)-2-amino-2-butenoyl-L-valyl-(3S,4E)-3-hydroxy-7-mercapto-4-heptenoyl-D-valyl-D-cysteinyl],cyclic (3®5)-disulfide (BioCAD00000179699)
Metabolite Card
Formula: C24H36N4O6S2 (540.2076)
SMILES: CC=C1NC(=O)C2CSSCCC=CC(CC(=O)NC(C(C)C)C(=O)N2)OC(=O)C(NC1=O)C(C)C
Synonyms [en]
istodax; L-Valine, N-(3-hydroxy-7-mercapto-1-oxo-4-heptenyl)-D-valyl-D-cysteinyl-(Z)-2,3-didehydro-2-aminobutanoyl-, xi-lactone, cyclic (1-2)-disulfide, (S-(E))-; romidepsin; 7-ethylidene-4,21-bis(propan-2-yl)-2-oxa-12,13-dithia-5,8,20,23-tetraazabicyclo[8.7.6]tricos-16-ene-3,6,9,19,22-pentone; 7-ethylidene-4,21-diisopropyl-2-oxa-12,13-dithia-5,8,20,23-tetraazabicyclo[8.7.6]tricos-16-ene-3,6,9,19,22-pentone; NCI60_009796
Last reviewed on 2024-06-28.
Cite this Page
Cyclo[(2Z)-2-amino-2-butenoyl-L-valyl-(3S,4E)-3-hydroxy-7-mercapto-4-heptenoyl-D-valyl-D-cysteinyl],cyclic (3¬¨¬®‚àö√ú5)-disulfide. 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: BioCAD00000179699). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
Romidepsin is a drug that has been approved by the U.S. Food and Drug Administration (FDA) under the brand name Istodax for the treatment of a certain type of cancer. Romidepsin is also being studied as an investigational drug as part of a strategy to cure HIV infection.As an HIV investigational drug, romidepsin belongs to a group of drugs called latency-reversing agents. Romidepsin is a selective inhibitor of histone deacetylase, approved in the US in 2009 for the treatment of cutaneous T-cell lymphoma (CTCL) in patients who have received at least one prior systemic therapy. Romidepsin is an intravenously administered histone deacetylase inhibitor and antineoplastic agent that is approved for use in refractory or relapsed cutaneous and peripheral T cell lymphomas. Romidepsin is associated with modest rate of minor serum enzyme elevations during therapy but has not been linked to cases of clinically apparent liver injury, although it has been reported to cause reactivation of hepatitis B. Romidepsin is a bicyclic depsipeptide antibiotic isolated from the bacterium Chromobacterium violaceum with antineoplastic activity. After intracellular activation, romidepsin binds to and inhibits histone deacetylase (HDAC), resulting in alterations in gene expression and the induction of cell differentiation, cell cycle arrest, and apoptosis. This agent also inhibits hypoxia-induced angiogenesis and depletes several heat shock protein 90 (Hsp90)-dependent oncoproteins.
DBLinks
- CAS Registry Number: 128517-07-7
- PubChem CID: 3425
- ChEBI:
- HMDB: HMDB0250632
- LipidMaps:
- KEGG:
- BioCyc:
- NCBI MeSH: romidepsin
- Wikipedia: Romidepsin
Other DBLinks
- CAS Registry Number: 128517-07-7
- PubChem: 3425
- HMDB: HMDB0250632
- NCBI MeSH: romidepsin
- Wikipedia: Romidepsin
- DrugBank: DB06176
Class / Ontology
- WishartLab ClassyFire: [Depsipeptides] Depsipeptides
Taxonomy Source
Pathway Synthetic
| pathway id | name |
|---|---|
| PathBank:SMP0000778 | Nitrogen Metabolism |
| PathBank:SMP0121260 | Nitrogen Metabolism |
| PathBank:SMP0002378 | Sphingolipid Metabolism |
| PathBank:SMP0002438 | Cholesterol Biosynthesis and Metabolism CE(12:0) |
| PathBank:SMP0002381 | Steroid Biosynthesis |
| PathBank:SMP0002436 | Cholesterol biosynthesis and metabolism CE(10:0) |
| PathBank:SMP0002441 | Cholesterol biosynthesis and metabolism CE(18:0) |
| PathBank:SMP0070041 | Cholesterol Biosynthesis and Metabolism |
| PathBank:SMP0002355 | Pyruvate Metabolism |
| PathBank:SMP0002435 | Cholesterol biosynthesis and metabolism CE(14:0) |
| PathBank:SMP0002440 | Cholesterol Biosynthesis and Metabolism CE(16:0) |