mycophenolate mofetil
A carboxylic ester resulting from the formal condensation between the carboxylic acid group of mycophenolic acid and the hydroxy group of 2-(morpholin-4-yl)ethanol. In the liver, it is metabolised to mycophenolic acid, an immunosuppressant for which it is a prodrug. It is widely used to prevent tissue rejection following organ transplants as well as for the treatment of certain autoimmune diseases.
Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.
Classification
Chemical structure
| Molecular formula | C23H31NO7 |
|---|---|
| Charge | 0 |
| Average mass | 433.501 Da |
| Monoisotopic mass | 433.21005 Da |
| Source | ChEBI |
| InChIKey | RTGDFNSFWBGLEC-SYZQJQIISA-N |
COc1c(C)c2c(c(O)c1C/C=C(\C)CCC(=O)OCCN1CCOCC1)C(=O)OC2
InChI=1S/C23H31NO7/c1-15(5-7-19(25)30-13-10-24-8-11-29-12-9-24)4-6-17-21(26)20-18(14-31-23(20)27)16(2)22(17)28-3/h4,26H,5-14H2,1-3H3/b15-4+
Also called
- Cellcept
- 2-(morpholin-4-yl)ethyl (4E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydro-2-benzofuran-5-yl)-4-methylhex-4-enoate
- 2-morpholinoethyl (E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-5-phthalanyl)-4-methyl-4-hexenoate
- MMF
- RS 61443
- mycophenolic acid morpholinoethyl ester
Cross-references
- cas:128794-94-5
- hmdb:HMDB0014826
- kegg.compound:C07908
- reaxys:7500599
Drug registries
Patents and articles
Activity roles
- anticoronaviral agent
CHEBI:149553
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:8764 |
mycophenolate mofetil | antibioticmech:chebi-815ebc1095 |
2026-08-30 |
Mechanism summary
- Clinical status
- APPROVED
Curation history
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories