Oglufanide
DRACPC ID DRACPC0040
Active Ingredients Oglufanide
Description Glu-Trp is a dipeptide composed of L-glutamic acid and L-tryptophan joined by a peptide linkage. It has a role as a metabolite, an immunomodulator, an angiogenesis modulating agent and an antineoplastic agent. It is functionally related to a L-glutamic acid and a L-tryptophan.
Synonyms Glu-trp; Glutamyltryptophan; L-Tryptophan, L-alpha-glutamyl-; Thymogen; Oglufanide
Type Small Molecule
Disease Colorectal Cancer, Ovarian Cancer, Kaposi's Sarcoma
Classification
Immunomodulator Peptide and derivative
Structure Information
Molecular Formula C16H19N3O5
Molecular Weight 333.34
Active Sequence EW
Sequence Length 2
Modification Not available
IUPAC Name (4S)-4-amino-5-[[(1S)-1-carboxy-2-(1H-indol-3-yl)ethyl]amino]-5-oxopentanoic acid
InChI InChI=1S/C16H19N3O5/c17-11(5-6-14(20)21)15(22)19-13(16(23)24)7-9-8-18-12-4-2-1-3-10(9)12/h1-4,8,11,13,18H,5-7,17H2,(H,19,22)(H,20,21)(H,23,24)/t11-,13-/m0/s1
InChI_Key LLEUXCDZPQOJMY-AAEUAGOBSA-N
SMILES O=C(O)CC[C@H](N)C(N[C@H](C(O)=O)CC1=CNC2=C1C=CC=C2)=O
External Codes
PubChem CID 100094
DrugBank Accession Number DB05779
NCI Thesaurus Code C76274
UNII 4RHY598T5U GSRS
CAS 38101-59-6
Drug approval
Drug indication
Investigated for use/treatment in hepatitis (viral, C) and cancer.
The drug is not approved.
ClinicalTrials.gov Identifier | Title | Condition or disease | Phase | Purpose |
---|---|---|---|---|
NCT00003773 | Phase I Study of Escalating Doses of IM-862 in Patients With Ovarian Cancer | Ovarian Cancer | Phase 1 | Treatment |
NCT00006037 | Phase II Randomized Placebo-Controlled Double-Blinded Study With 5-FU vs. 5-FU With IM862 With Cross-Over to CPT-11 vs. CPT-11 With IM862 | Colorectal Cancer | Phase 2 | Treatment |
NCT00017303 | A Phase II Trial Of IM862 Combined With Paclitaxel And Carboplatin In Newly Diagnosed Advanced Epithelial Ovarian Or Primary Peritoneal Carcinoma Followed By IM862 Consolidation Therapy | Ovarian Cancer; Primary Peritoneal Cavity Cancer | Phase 2 | Treatment |
More clinical information is obtained from ClinicalTrials.gov.