Structure via PubChem · Public domain (PubChem)
In the Vinony graph
Within Vinony's link graph, melphalan flufenamide is referenced by 272 other articles, and connects out to chemotherapy, tiazofurin and public domain.
It sits within the topics Alkylating agents, Cancer treatments and Dipeptides.
Its subject is documented across 5 Wikipedia language editions.
Chemical data
- Formula
- C24H30Cl2FN3O3
- Molecular weight
- 498.4 g/mol
- IUPAC name
- ethyl (2S)-2-[[(2S)-2-amino-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoyl]amino]-3-(4-fluorophenyl)propanoate
- SMILES
- CCOC(=O)[C@H](CC1=CC=C(C=C1)F)NC(=O)[C@H](CC2=CC=C(C=C2)N(CCCl)CCCl)N
- InChIKey
- YQZNKYXGZSVEHI-VXKWHMMOSA-N
- XLogP
- 3.2
- Polar surface area
- 84.7 Ų
- H-bond donors
- 2
- H-bond acceptors
- 6
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 497.165
Show 4 more facts
- canonical SMILES
- CCOC(=O)C(CC1=CC=C(C=C1)F)NC(=O)C(CC2=CC=C(C=C2)N(CCCl)CCCl)N
- chemical formula
- C₂₄H₃₀Cl₂FN₃O₃
- isomeric SMILES
- CCOC(=O)[C@H](CC1=CC=C(C=C1)F)NC(=O)[C@H](CC2=CC=C(C=C2)N(CCCl)CCCl)N
- Commons category
- Melphalan flufenamide
Sources (1)
via Wikidata · CC0
Connections
chemotherapy
Entity
tiazofurin
Entity
public domain
Entity
digital object identifier
Entity
chemical formula
Entity
molar mass
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hydrolysis
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PubMed
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DNA replication
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phenylalanine
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hydrazine
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cell cycle
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DL-asparagine
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CAS Registry Number
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multiple myeloma
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PubMed Central
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PubChem
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United States Food and Drug Administration
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Anatomical Therapeutic Chemical Classification System
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microtubule
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