DESACETYLVINBLASTINEAMIDE
DESACETYLVINBLASTINEAMIDE Basic information
- Product Name:
- DESACETYLVINBLASTINEAMIDE
- Synonyms:
-
- VINDESINE
- 3-(aminocarbonyl)-o(sup4)-deacetyl-3-de(methoxycarbonyl)-vincaleukoblastin
- 3-(aminocarbonyl)-o(sup4)-deacetyl-3-de(methoxycarbonyl)vincaleukoblastine
- DESACETYLVINBLASTINEAMIDE
- Fildesin
- Compound 112531:NS C.245467:LY-099094:Hdisine:Fildisin
- VDS
- Vincaleukoblastine, 3-(aminocarbonyl)-O4-deacetyl-3-de(methoxycarbonyl)-
- CAS:
- 53643-48-4
- MF:
- C43H55N5O7
- MW:
- 753.93
- EINECS:
- 258-682-2
- Mol File:
- 53643-48-4.mol
DESACETYLVINBLASTINEAMIDE Chemical Properties
- Melting point:
- 230-232°
- alpha
- D25 +39.4° (c = 1.0 in methanol)
- Density
- 1.41±0.1 g/cm3(Predicted)
- pka
- pKa (DMF 66%) 5.39, 7.36; (H2O) 6.04, 7.67(at 25℃)
Safety Information
- RIDADR
- 1544
- HazardClass
- 6.1(a)
- PackingGroup
- II
- Hazardous Substances Data
- 53643-48-4(Hazardous Substances Data)
DESACETYLVINBLASTINEAMIDE Usage And Synthesis
Originator
Eldisine,Lilly ,France,1980
Uses
Antineoplastic.
Definition
ChEBI: Vindesine is a vinca alkaloid, a methyl ester, an organic heterotetracyclic compound, an organic heteropentacyclic compound, a tertiary alcohol, a tertiary amino compound and a primary carboxamide. It has a role as an antineoplastic agent. It is functionally related to a vincaleukoblastine.
Manufacturing Process
About 10 g of VLB (vincaleucoblastine or simply vinblastine) sulfate were converted by standard procedures to VLB free base. The free base, obtained as a residue after evaporation of the dried ethereal solvent, was dissolved in about 200 ml of anhydrous methanol. Anhydrous liquid ammonia (300 ml) was added, and the reaction mixture sealed and maintained at about 100°C for 60 hours. The reaction vessel was opened, and the contents removed and evaporated to dryness in vacuo. The resulting residue, containing 4-desacetyI VLB C-3 carboxamide, as shown by thin layer chromatography, were combined and the solvent evaporated therefrom in vacuo, yielding asa residue purified 4-desacetyl VLB C-3 carboxamide free base. The NMR and IR spectra of the solid free base confirmed the structure indicated. The free base showed a band in the infrared at 1,687 cm -l , characteristic of the amide function. The molecular weight of the free base determined by mass spectroscopy was 753 which is in agreement with theoretical value calculated for C 43 H 55 N 5 O 7 .
brand name
Eldisine (Lilly).
Therapeutic Function
Antineoplastic
DESACETYLVINBLASTINEAMIDE Preparation Products And Raw materials
Raw materials
DESACETYLVINBLASTINEAMIDESupplier
- Tel
- 028-83311324 1278112614
- climaxbiotech@gmail.com
- Tel
- +86-021-50935922
- Tel
- +86 (20) 28996708,29078958,28139708,29076128,28133708,28139728,28139738,28133718,021-31663278,021-31663578,021-60538387
- Tel
- 028-81700200 18116577057
- 3003855609@qq.com
- Tel
- 400-1166-196 13458535857
- cdhxsj@163.com
DESACETYLVINBLASTINEAMIDE(53643-48-4)Related Product Information
- Vinblastine sulfate
- Vincristine
- Dexrazoxane
- Vinorelbine tartrate
- Vindesine sulfate
- 1,3,3,5,5-PENTAMETHYLCYCLOHEXANOL
- TRIMETHYLHEXAMETHYLENEDIAMINE
- TRANS-2-AMINOMETHYL-1-CYCLOHEXANOL
- DESACETYLVINBLASTINEAMIDE
- P-(TRANS-4-HYDROXYCYCLOHEXYL)PHENOL
- (2-METHOXY-5-METHYLPHENYL)ACETIC ACID
- TRANS-2-HYDROXY-1-CYCLOHEXANECARBOXAMIDE
- CIS-2-AMINO-1-CYCLOHEXANECARBOXAMIDE
- 1-(2-(2-Methyl-1H-indol-3-yl)ethyl)-3-piperidinol
- 2-METHOXY-5-METHYL-BENZENEACETIC ACID METHYL ESTER
- Propionic acid, 2-(4-(isopropylamino)phenyl)-
- 2-Methyl-3-(2-(3-methyl-1-piperidinyl)ethyl)-1H-indole
- 2,4-BIS(1-METHYLBUTYL)PHENOL