BBM-928 A

BBM-928 A Suppliers list
Company Name: BOC Sciences
Tel: +16314854226
Email: inquiry@bocsci.com
Products Intro: Product Name:Luzopeptin A
CAS:75580-37-9
Purity:>99% by HPLC Remarks:BOC Sciences also provides custom synthesis services for Luzopeptin A.
Company Name: Aladdin Scientific
Tel: +1-833-552-7181
Email: sales@aladdinsci.com
Products Intro: Product Name:Luzopeptin A
CAS:75580-37-9
Purity:>99% Package:$1099.9/1mg;Bulk package Remarks:>99%
Company Name: Lynnchem  
Tel: 86-(0)29-85992781 17792393971
Email: info@lynnchem.com
Products Intro: Product Name:BBM-928 A
CAS:75580-37-9
Purity:>99% by HPLC Package:1mg;5mg
Company Name: Novachemistry  
Tel: 44-20819178-90 02081917890
Email: info@novachemistry.com
Products Intro: Product Name:Luzopeptin A
CAS:75580-37-9
Purity:>99% by HPLC Package:1mg;5mg
Company Name: Shenzhen Polymeri Biochemical Technology Co., Ltd.  
Tel: +86-400-002-6226 13028896684
Email: sales@rrkchem.com
Products Intro: Product Name:Luzopeptin A
CAS:75580-37-9
BBM-928 A Basic information
Product Name:BBM-928 A
Synonyms:BBM-928 A;2-Quinolinecarboxamide, N,N'-[4,23-bis(acetyloxy)-4,4A,5,6,7,8,9,10,11,12,13,14,17,18,23,23A,24,25,26,27,28,29,30,31,32,33,36,37-octacosahydro-13,32-bis(1-hydroxy-1-methylethyl)-9,12,28,31-tetramethyl-5,8,11,14,18,24,27,30,33,37-decaoxo-3H,16H,22H,35H-dipyridazino[6,1-L:6',1'-B1][1,17,4,7,10,13,20,23,26,29]dioxaoctaazacyclodotriacontine-17,36-diyl]bis[3-hydroxy-6-methoxy-, [4S-(4R*,4ar*,13R*,17S*,23R*,23ar*,32R*,36S*)]-;85255-31-8 (Deleted);Aids082344;Aids-082344;Antibiotic bbm 928C, 2,7-diacetate;Antibiotic bbm-928a;Diacetyl-luzopeptin c
CAS:75580-37-9
MF:C64H78N14O24
MW:1427.38
EINECS:
Product Categories:
Mol File:75580-37-9.mol
BBM-928 A Structure
BBM-928 A Chemical Properties
density 1.50±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO;Soluble in dimethyl formamide
form solid
pka6.75±0.40(Predicted)
color tan
Safety Information
MSDS Information
BBM-928 A Usage And Synthesis
UsesLuzopeptin A is an inhibitor of HIV-1 and HIV-2 reverse transcriptase.
UsesLuzopeptin A is a cyclic depsipeptide antibiotic first isolated from an actinomycete strain. It displays antitumor activity, as it is highly active in mice against a variety of experimental tumors. Luzopeptin A acts as a bifunctional DNA intercalator that strongly binds DNA and forms crosslinks between DNA molecules. It also inhibits reverse transcriptases from HIV-1 and HIV-2 (IC50s = 7 and 68 nM, respectively), as well as cellular DNA polymerases.[Cayman Chemical]
UsesLuzopeptin A is a member of the echinomycin (quinomycin A) class of antitumor and antibiotic agents that act by forming a stable DNA complex by bis-intercalation. Luzopeptin A is alsoa potent inhibitor of HIV-1 reverse transcriptase.
Biological Activityluzopeptin a is a cyclic depsipeptide antibiotic.a depsipeptide is a peptide in which one or more of its amide groups are replaced by the corresponding ester, or more generally, is a molecule that has both peptide and ester linkages in proximity in the same amino acid-containing small molecule or chain.
in vitroprevious study found that luzopeptin a treatment could produce additional dna bands which were the products of type ii biintercalation. the types of restriction fragments involved were identified. maximal type ii biintercalation occurred at a luzopeptin a/dna range of 0.14 to 0.18, at which more than 50% of the total dna molecules were involved. type ii products were gradually converted to type i products upon prolonged incubation at 37 degrees, maybe due to the tendency for intermolecular bonds to disrupt. echinomycin treatment failed to produce type ii products, probably because of a dna-binding affinity weaker than that of luzopeptin a [1].
in vivoanimal study showed that when administered as a suspension in 0.9% nacl solution, luzopeptin a demonstrated good activity against i.p. b16 melanoma and i.p. p388 leukemia and weak activity versus i.v. p388, i.p. l1210 leukemia, lewis lung, and madison 109 lung carcinomas. in terms of tumor cell kill, luzopeptin a induced net reductions in the body burdens of l1210 and p388 leukemias following single-drug injections but failed to yield net reductions following multiple-injection therapies [2].
references[1] huang, c. h.,mirabelli, c.k.,mong, s., et al. intermolecular cross-linking of dna through bifunctional intercalation of an antitumor antibiotic, luzopeptin a (bbm-928a). cancer research 43, 2718-2724 (1983).
[2] rose wc, schurig je, huftalen jb, bradner wt. experimental antitumor activity and toxicity of a new chemotherapeutic agent, bbm 928a. cancer res. 1983 apr;43(4):1504-10.
BBM-928 A Preparation Products And Raw materials
Tag:BBM-928 A(75580-37-9) Related Product Information
BBM-928 A BBM-928 B 6-METHOXY-QUINOLINE-2-CARBALDEHYDE 3-Hydroxyquinoline BBM-928 C (R)-2-Amino-3-hydroxy-3-methylbutanoic acid 3-HYDROXYPICOLINAMIDE