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REBECCAMYCIN

CAS No.
93908-02-2
Chemical Name:
REBECCAMYCIN
Synonyms
NSC 359079;chrysomycin;REBECCAMYCIN;dro-12-(4-o-methyl-beta-d-glucopyranosyl)-;REBECCAMYCIN, SACCHAROTHRIX AEROCOLONIGENES;5h-indolo(2,3-a)pyrrolo(3,4-c)carbazole-5,7(6h)-dione,1,11-dichloro-12,13-dihy;1,11-Dichloro-12,13-dihydro-12-(4-O-methyl-β-D-glucopyranosyl)-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-dione;5H-Indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-dione, 1,11-dichloro-12,13-dihydro-12-(4-O-methyl-β-D-glucopyranosyl)-;7,10-Dichloro-8-(3,4-dihydroxy-6-(hydroxymethyl)-5-methoxytetrahydro-2H-pyran-2-yl)-8,9-dihydro-1H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-1,3(2H)-dione
CBNumber:
CB7747508
Molecular Formula:
C27H21Cl2N3O7
Molecular Weight:
570.38
MDL Number:
MFCD23105147
MOL File:
93908-02-2.mol
MSDS File:
SDS
Last updated:2023-06-30 15:45:59

REBECCAMYCIN Properties

storage temp. −20°C
solubility DMSO: ≥3 mg/mL
form solid
color yellow
NCI Dictionary of Cancer Terms rebeccamycin
FDA UNII Y96MQM21V9

SAFETY

Risk and Safety Statements

WGK Germany  -

REBECCAMYCIN price More Price(6)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 17914 Rebeccamycin ≥99% 93908-02-2 500μg $178 2024-03-01 Buy
Cayman Chemical 17914 Rebeccamycin ≥99% 93908-02-2 2.5mg $793 2024-03-01 Buy
TRC R140000 Rebeccamycin 93908-02-2 0.5mg $125 2021-12-16 Buy
Usbiological 207378 Rebeccamycin 93908-02-2 250ug $337 2021-12-16 Buy
Usbiological R1281-15 Rebeccamycin 93908-02-2 500ug $482 2021-12-16 Buy
Product number Packaging Price Buy
17914 500μg $178 Buy
17914 2.5mg $793 Buy
R140000 0.5mg $125 Buy
207378 250ug $337 Buy
R1281-15 500ug $482 Buy

REBECCAMYCIN Chemical Properties,Uses,Production

Uses

Rebeccamycin is a novel indolocarbazole topoisomerase I inhibitor.

Uses

Rebeccamycin is an indolocarbazole isolated from Lechevalieria aerocolonigenes. Rebeccamycin displays selective antitumour activity against several cell lines. Rebeccamycin's primary mechanism of action is via strong DNA intercalation resulting in the potent catalytic inhibition of both topoisomerases I and II. Analogues of rebecamycin have beend tested in clinical trials for cancer therapy.

Definition

ChEBI: An N-glycosyl compound consisting of a heteropolycyclic ring system with a glucosyl group attached to one of the indolic nitrogens.

storage

+4°C

REBECCAMYCIN Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 61)Suppliers
Supplier Tel Email Country ProdList Advantage
Fuxin Pharmaceutical
+86-021-021-50872116 +8613122107989 contact@fuxinpharm.com China 10297 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
BOC Sciences
+16314854226 inquiry@bocsci.com United States 19743 58
Shaanxi Cuikang Pharmaceutical Technology Co., Ltd
+86-19164747840 +86-13119157289 13119157289@163.com China 2971 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 52927 58
Shanghai Tauto Biotech Co., Ltd. 021-51320588 tauto@tautobiotech.com China 3989 66
Guangzhou Isun Pharmaceutical Co., Ltd 020-39119399 18927568969 isunpharm@qq.com China 4428 55
ChemStrong Scientific Co.,Ltd 0755-66853366 13670046396 sales@chem-strong.com China 17982 56
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9709 58
Beijing Jin Ming Biotechnology Co., Ltd. 010-60605840 18892239720 psaitong@jm-bio.com China 12308 58
5h-indolo(2,3-a)pyrrolo(3,4-c)carbazole-5,7(6h)-dione,1,11-dichloro-12,13-dihy dro-12-(4-o-methyl-beta-d-glucopyranosyl)- REBECCAMYCIN REBECCAMYCIN, SACCHAROTHRIX AEROCOLONIGENES 1,11-Dichloro-12,13-dihydro-12-(4-O-methyl-β-D-glucopyranosyl)-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-dione NSC 359079 7,10-Dichloro-8-(3,4-dihydroxy-6-(hydroxymethyl)-5-methoxytetrahydro-2H-pyran-2-yl)-8,9-dihydro-1H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-1,3(2H)-dione 5H-Indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-dione, 1,11-dichloro-12,13-dihydro-12-(4-O-methyl-β-D-glucopyranosyl)- chrysomycin 93908-02-2 C27H21Cl2N3O7 BioChemical Antibiotics A to Z Antibiotics Antibiotics N-S