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Luzopeptin A is a cyclic depsipeptide antibiotic produced by an actinomycete strain. It has anti-tumor activity. It is a potent inhibitor of HIV-1 reverse transcriptase. Synonyms: Luzopeptin A; 75580-37-9; Bbm-928 A; BBM-928A; Diacetyl-luzopeptin C; [(3R,7S,16S,17S,23R,27S,36S,37S)-37-acetyloxy-3,23-bis[(3-hydroxy-6-methoxyquinoline-2-carbonyl)amino]-7,27-bis(2-hydroxypropan-2-yl)-8,11,28,31-tetramethyl-2,6,9,12,15,22,26,29,32,35-decaoxo-5,25-dioxa-1,8,11,14,20,21,28,31,34,40-decazatricyclo[34.4.0.016,21]tetraconta-19,39-dien-17-yl] acetate; Luzopeptin C, 2,7-diacetate; Antibiotic BBM 928C, 2,7-diacetate; [37-Acetyloxy-3,23-bis[(3-hydroxy-6-methoxyquinoline-2-carbonyl)amino]-7,27-bis(2-hydroxypropan-2-yl)-8,11,28,31-tetramethyl-2,6,9,12,15,22,26,29,32,35-decaoxo-5,25-dioxa-1,8,11,14,20,21,28,31,34,40-decazatricyclo[34.4.0.016,21]tetraconta-19,39-dien-17-yl] acetate; Antibiotic BBM 928A; BRN 5725577; BBM 928A; SCHEMBL20614463; CHEBI:223532; DTXSID401317872; NSC308312; HY-130050; CS-0104626. Grade: >99% by HPLC. CAS No. 75580-37-9. Molecular formula: C24H32O6. Mole weight: 416.5.
Luzopeptin A (Antibiotic BBM-928A)
Luzopeptin is a member of the echinomycin (quinomycin A) class of antitumor and antibiotic agents that act by formation of a stable DNA complex by bis-intercalation. Luzopeptin A has also been shown to be a potent inhibitor of HIV-1 reverse transcriptase. Group: Biochemicals. Alternative Names: Antibiotic BBM-928A. Grades: Highly Purified. CAS No. 75580-37-9. Pack Sizes: 1mg. US Biological Life Sciences.
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(1R, 2R) -2- methyl cyclopropanecarboxylic Acid
(1R, 2R) -2- methyl cyclopropanecarboxylic Acid, is an intermediate used for the synthesis of (1R,2R)-trans-1-(Chloromethyl)-2-methylcyclopropane (C369820). It can also be used for the preparation of Luzopeptin A-C and Quinoxapeptin A-C, acting as potent inhibitors of HIV-1 reverse transcriptase. Group: Biochemicals. Grades: Highly Purified. CAS No. 10487-86-2. Pack Sizes: 500mg, 5g. Molecular Formula: C5H8O2, Molecular Weight: 100.12. US Biological Life Sciences.
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Quinaldopeptin
It is a symmetrical, cyclic decapeptide from an amycolatopsis sp. This is a bis-intercalator of DNA. It exhibits strong in vitro antimicrobial and cytotoxic activity. It significantly prolongs the survival time of mice inoculated with a murine tumour, and also shows weak nematocidal activity. It is related to the luzopeptins and sandramycin. Synonyms: Antibiotic BMY 28662; Antibiotic BU 3845T; BMY 28662; BU 3845T. Grade: >95% by HPLC. CAS No. 130743-07-6. Molecular formula: C62H78N14O14. Mole weight: 1243.37.
Quinaldopeptin (Antibiotic BMY 28662, Antibiotic BU 3845T)
Quinaldopeptin is a symmetrical cyclic decapeptide from an Amycolatopsis sp. that is a bis-intercalator of DNA. It exhibits strong in vitro antimicrobial and cytotoxic activity and significantly prolonged the survival time of mice inoculated with a murine tumor. Quinaldopeptin also shows weak nematocidal activity and is related to the luzopeptins and sandramycin. Group: Biochemicals. Alternative Names: Antibiotic BMY 28662, Antibiotic BU 3845T. Grades: Highly Purified. CAS No. 130743-07-6. Pack Sizes: 500ug. US Biological Life Sciences.
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