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Safusidenib

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Pharmaceutical compound
Safusidenib
Clinical data
Other namesAB-218; DS-1001; DS-1001b
Legal status
Legal status
  • investigational
Identifiers
  • (E)-3-[1-[5-(2-fluoropropan-2-yl)-3-(2,4,6-trichlorophenyl)-1,2-oxazole-4-carbonyl]-3-methylindol-4-yl]prop-2-enoic acid
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
ChEBI
ChEMBL
Chemical and physical data
Formula C25H18Cl3FN2O4
Molar mass 535.78g·mol−1
3D model (JSmol)
  • CC1=CN(C2=CC=CC(=C12)/C=C/C(=O)O)C(=O)C3=C(ON=C3C4=C(C=C(C=C4Cl)Cl)Cl)C(C)(C)F
  • InChI=InChI=1S/C25H18Cl3FN2O4/c1-12-11-31(17-6-4-5-13(19(12)17)7-8-18(32)33)24(34)21-22(30-35-23(21)25(2,3)29)20-15(27)9-14(26)10-16(20)28/h4-11H,1-3H3,(H,32,33)/b8-7+
  • Key:BOOMBLZEOHXPPX-BQYQJAHWSA-N

Safusidenib is an investigational new drug that is being evaluated by AnHeart Therapeutics and the Daiichi Sankyo Company for the treatment of IDH1-mutant glioma. It is a isocitrate dehydrogenase 1 inhibitor.[1] [2]

Clinical trials

[edit ]

Safusidenib is in phase 3 clinical trials for IDH1-mutant glioma.[3]

References

[edit ]
  1. "Safusidenib - Daiichi Sankyo Company; National Cancer Center (Tokyo)". AdisInsight. Springer Nature Switzerland AG.
  2. Lanman TA, Gonzalez Castro LN (August 2025). "Targeting of Mutant Isocitrate Dehydrogenase in Glioma: A Systematic Review". Cancers. 17 (16). Basel: 2630. doi:10.3390/cancers17162630 . PMC 12384762 . PMID 40867259.
  3. Clinical trial number NCT05303519 for "SIGMA (Safusidenib in IDH1 Mutant Glioma Maintenance)" at ClinicalTrials.gov
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