Camsirubicin hydrochlorideProduct ingredient for Camsirubicin
- Name
- Camsirubicin hydrochloride
- Drug Entry
- Camsirubicin
GPX-150 has been used in trials studying the treatment of Soft Tissue Sarcoma and Advanced Solid Tumors - Phase 1 Population.
- Accession Number
- DBSALT003284
- Structure
Structure for Camsirubicin hydrochloride (DBSALT003284)
- Synonyms
- 5-imino-13-deoxydoxorubicin HCl / 5(8H)-NAPHTHACENONE, 10-((3-AMINO-2,3,6-TRIDEOXY-.ALPHA.-L-LYXO-HEXOPYRANOSYL)OXY)-7,9,10,12-TETRAHYDRO-6,8,11-TRIHYDROXY-8-(2-HYDROXYETHYL)-12-IMINO-1-METHOXY-, MONOHYDROCHLORIDE, (8R,10S)- / GPX-150 HYDROCHLORIDE
- UNII
- QFO4NOX87K
- CAS Number
- 236095-24-2
- Weight
- Average: 565.02
Monoisotopic: 564.1874584 - Chemical Formula
- C27H33ClN2O9
- InChI Key
- QVPRMGHPBJJSRU-IGAJXZAQSA-N
- InChI
- InChI=1S/C27H32N2O9.ClH/c1-11-23(31)14(28)8-17(37-11)38-16-10-27(35,6-7-30)9-13-19(16)26(34)20-21(25(13)33)24(32)12-4-3-5-15(36-2)18(12)22(20)29;/h3-5,11,14,16-17,23,29-31,33-35H,6-10,28H2,1-2H3;1H/t11-,14-,16-,17-,23+,27-;/m0./s1
- IUPAC Name
- (8R,10S)-10-{[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy}-6,8,11-trihydroxy-8-(2-hydroxyethyl)-12-imino-1-methoxy-5,7,8,9,10,12-hexahydrotetracen-5-one hydrochloride
- SMILES
- Cl.[H][C@@]1(C[C@H](N)[C@H](O)[C@H](C)O1)O[C@H]1C[C@](O)(CCO)CC2=C(O)C3=C(C(O)=C12)C(=N)C1=C(OC)C=CC=C1C3=O
- External Links
- ChemSpider
- 81368314
- Predicted Properties
Property Value Source logP 1.26 Chemaxon pKa (Strongest Acidic) 10.29 Chemaxon pKa (Strongest Basic) 9.46 Chemaxon Physiological Charge 1 Chemaxon Hydrogen Acceptor Count 11 Chemaxon Hydrogen Donor Count 7 Chemaxon Polar Surface Area 195.78 Å2 Chemaxon Rotatable Bond Count 5 Chemaxon Refractivity 146.74 m3·mol-1 Chemaxon Polarizability 54.49 Å3 Chemaxon Number of Rings 5 Chemaxon Bioavailability 0 Chemaxon Rule of Five No Chemaxon Ghose Filter No Chemaxon Veber's Rule No Chemaxon MDDR-like Rule No Chemaxon