(R)-Melphalan
drugOn this page
Also known as SID11111435
Summary
(R)-Melphalan (CHEMBL250892) is a phase-3 clinical-stage small molecule; indicated across 2 conditions including ewing sarcoma and plasma cell myeloma.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Small molecule
- Indications: 2 conditions
- Chemistry: 305.2 Da · C13H18Cl2N2O2
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL250892 |
| Name | (R)-Melphalan |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | no |
| PubChem CID | 20189 |
| Molecular formula | C13H18Cl2N2O2 |
| Molecular weight | 305.2 |
| InChIKey | SGDBTWWWUNNDEQ-GFCCVEGCSA-N |
SMILES: C1=CC(=CC=C1C[C@H](C(=O)O)N)N(CCCl)CCCl
IUPAC name: (2R)-2-amino-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid
Also known as: (r)-melphalan, SID11111435, (R)-MELPHALAN
Patent coverage: 6,644 distinct patent families (23,925 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Broader ChEMBL bioactivity targets: 6 (assay-derived). Sample: Thrombopoietin, Muscarinic acetylcholine receptor M1, Nuclear factor NF-kappa-B p105 subunit, Cytochrome P450 1A2, Cytochrome P450 3A4, Hypoxia-inducible factor 1-alpha.
Bioactivity
ChEMBL activities: 9 potent at pChembl ≥ 5 of 11 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| NFKB1 | 5.2 | Potency | 6310 | nM | CHEMBL_ACT_3671922 |
| NFKB1 | 5.2 | Potency | 6310 | nM | CHEMBL_ACT_4585204 |
| THPO | 5.2 | Potency | 6310 | nM | CHEMBL_ACT_4809381 |
| THPO | 5.2 | Potency | 6310 | nM | CHEMBL_ACT_5070392 |
| HIF1A | 5 | Potency | 10000 | nM | CHEMBL_ACT_4132675 |
| HIF1A | 5 | Potency | 10000 | nM | CHEMBL_ACT_4519444 |
| CYP3A4 | 5 | Potency | 10000 | nM | CHEMBL_ACT_4949232 |
| CYP3A4 | 5 | Potency | 10000 | nM | CHEMBL_ACT_5078581 |
| CYP3A4 | 5 | AC50 | 10000 | nM | CHEMBL_ACT_6009666 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
2 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| Ewing sarcoma | 3 | MONDO:0012817 | EFO:0000174 |
| plasma cell myeloma | 3 | MONDO:0009693 | EFO:0001378 |
Clinical trials
Total trials: 0.
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: Ewing sarcoma, plasma cell myeloma