ChemicalBook >> CAS DataBase List >>Stallimycin

Stallimycin

CAS No.
636-47-5
Chemical Name:
Stallimycin
Synonyms
Distamycin;Stallimycin;Distamycin-3;3-[4-[4-[4-(Formylamino)-1-methyl-1H-pyrrole-2-ylcarbonylamino]-1-methyl-1H-pyrrole-2-ylcarbonylamino]-1-methyl-1H-pyrrole-2-ylcarbonylamino]propanamidine;N-[5-[[(3-Amino-3-iminopropyl)amino]carbonyl]-1-methyl-1H-pyrrol-3-yl]-4-[[[4-(formylamino)-1-methyl-1H-pyrrol-2-yl]carbonyl]amino]-1-methyl-1H-pyrrole-2-carboxamide;1H-Pyrrole-2-carboxamide, N-[5-[[(3-amino-3-iminopropyl)amino]carbonyl]-1-methyl-1H-pyrrol-3-yl]-4-[[[4-(formylamino)-1-methyl-1H-pyrrol-2-yl]carbonyl]amino]-1-methyl-
CBNumber:
CB51179775
Molecular Formula:
C22H27N9O4
Molecular Weight:
481.51
MDL Number:
MOL File:
636-47-5.mol
Last updated:2022-12-21 16:56:50

Stallimycin Properties

Melting point 154-156°
Boiling point 579.2°C (rough estimate)
Density 1.3298 (rough estimate)
refractive index 1.6910 (estimate)
EWG's Food Scores 1
FDA UNII 80O63P88IS

Stallimycin Chemical Properties,Uses,Production

Originator

Herperal,Farmitalia,Italy,1978

Manufacturing Process

A spore suspension obtained upon washing a culture of Streptomyces distallicus is added to 3,000 ml of a sterile medium consisting of the following:Dextrose 2% Corn steep liquor extract 2% CaCO3 1% (NH4)2SO4 0.3% NaCl 0.3%Fermentation is continued at 28°C for 40 hours at a stirring rate of 150 to 250 rpm and a rate of air flow of 1 to 2 l/min/l of culture medium.
300 ml of a suspension of the vegetative mycelium of this culture are used for inoculating 6,000 ml of a similar sterile culture medium. At this production stage, the culture is kept fermenting for 85 to 100 hours (pH 7.6 at 28°C) at a stirring rate of 350 to 450 rpm and a rate of air flow of 1 to 1.5 l/min/l of culture medium.
To 17 l of a culture obtained by submerged fermentation as mentioned above, siliceous earth is added and the batch is filtered. The mixture of mycelium and the siliceous earth are agitated for 1 hour with 2.5 l of butanol. This treatment is repeated twice. The butanolic extracts are combined, washed with water, evaporated to dryness (about 10 g) and boiled with acetone (80 ml). The 5 g of distamycin is extracted six times with ethanol. The ethanolic extracts are combined, concentrated and filtered through a column containing 70 g of alumina. Elution is carried out with the same solvent. The effluent (central fractions) is collected and evaporated to dryness to yield 0.43 g of pure distamycin A: decomposition point, 183°C to 185°C. The product can be further purified by crystallization from aqueous n-butanol.

Therapeutic Function

Antibiotic

Stallimycin Preparation Products And Raw materials

Raw materials

Preparation Products

Stallimycin Suppliers

Global( 9)Suppliers
Supplier Tel Email Country ProdList Advantage
BOC Sciences 1-631-485-4226; 16314854226 info@bocsci.com United States 14059 65
ChemStrong Scientific Co.,Ltd 0755-0755-66853366 13670046396 sales@chem-strong.com China 17994 56
Zhejiang Huida Biotech Co., LTD 0571-89903882 13626641628 jiangnan@huidabiotech.com China 3661 58
Hubei Zhongshan Medical Technology Co., Ltd 027-61907345 13397111514 w13397111514@163.com China 1006 58
Zhejiang Huida Biotech Co., LTD 0571-0571-89903882 15990081639 sunshixuan@huidabiotech.com China 3705 58
Hangzhou Hesheng Taiyi Biotechnology Co. , Ltd. 15868607770 hstysales@126.com China 1160 58
Shanghai Yanchun Biopharmaceutical Technology Co., Ltd 4001-009266 17349750668 product@sci-e.com China 2812 58
Hangzhou Huiyi Biotechnology Co., LTD 0571-89918262 13357170655 chenlingwei@hizyme.com China 556 58
Stallimycin 3-[4-[4-[4-(Formylamino)-1-methyl-1H-pyrrole-2-ylcarbonylamino]-1-methyl-1H-pyrrole-2-ylcarbonylamino]-1-methyl-1H-pyrrole-2-ylcarbonylamino]propanamidine Distamycin Distamycin-3 N-[5-[[(3-Amino-3-iminopropyl)amino]carbonyl]-1-methyl-1H-pyrrol-3-yl]-4-[[[4-(formylamino)-1-methyl-1H-pyrrol-2-yl]carbonyl]amino]-1-methyl-1H-pyrrole-2-carboxamide 1H-Pyrrole-2-carboxamide, N-[5-[[(3-amino-3-iminopropyl)amino]carbonyl]-1-methyl-1H-pyrrol-3-yl]-4-[[[4-(formylamino)-1-methyl-1H-pyrrol-2-yl]carbonyl]amino]-1-methyl- 636-47-5 C22H27N9O4