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esperamicin A1

CAS No.
99674-26-7
Chemical Name:
esperamicin A1
Synonyms
speramicin;esperamicin A1;Eesperamicin A1;Esperamicin A1 (BMY 28175);Carbamic acid, N-[(1R,4Z,8S,12S,13E)-8-[[4,6-dideoxy-2-O-[2,4-dideoxy-3-O-methyl-4-[(1-methylethyl)amino]-α-L-threo-pentopyranosyl]-4-[[(2,6-dideoxy-4-S-methyl-4-thio-β-D-ribo-hexopyranosyl)oxy]amino]-β-D-glucopyranosyl]oxy]-12-[[2,6-dideoxy-3-O-[4,5-dimethoxy-2-[(2-methoxy-1-oxo-2-propen-1-yl)amino...
CBNumber:
CB21371312
Molecular Formula:
C59H80N4O22S4
Molecular Weight:
1325.54
MDL Number:
MFCD34469160
MOL File:
99674-26-7.mol
MSDS File:
SDS
Last updated:2025-04-17 18:22:24

esperamicin A1 Properties

Density 1.43±0.1 g/cm3(Predicted)
pka 6.67±0.70(Predicted)
CAS DataBase Reference 99674-26-7
FDA UNII PLX8T21X8G

esperamicin A1 price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0011364 ESPERAMICIN A1 95.00% 99674-26-7 5MG $495.78 2021-12-16 Buy
Product number Packaging Price Buy
API0011364 5MG $495.78 Buy

esperamicin A1 Chemical Properties,Uses,Production

Uses

Esperamicin A1, as an extremely potent antitumor antibiotic, is isolated from cultures of Actinomadura verrucosospora. Esperamicin A1 can be used for the research of antitumor[1]. Eesperamicin A1 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

Definition

ChEBI: A naturally occurring antibiotic and antitumor agent isolated from Actinomadura verrucosopora. Its chemical structure consists of a core bicyclo[7.3.1]tridecadiynene moiety containing a 1,5-diyn-3-ene as part of a ten-membered ring, a lpha,beta-unsaturated ketone with a bridgehead double bond and an attached allylic trisulfide. This ring system is attached at one end by a trisaccharide moiety and at the opposite end by a 2-deoxy-L-fucose-anthra ilate moiety. The trisaccharide consists of a hydroxyamino sugar which is connected to a isopropylamino sugar through a glycosidic linkage and a thiomethyl sugar through an NH1O linkage.

References

[1] Lam, K. S., et al. Biosynthesis of esperamicin A1, an enediyne antitumor antibiotic. Journal of the American Chemical Society, 115(26), 12340–12345.

esperamicin A1 Preparation Products And Raw materials

Raw materials

Preparation Products

esperamicin A1 Suppliers

Global( 23)Suppliers
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BOC Sciences
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Shanghai Minbiotech Co., Ltd.
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AFINE CHEMICALS LIMITED
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ShangHai Caerulum Pharma Discovery Co., Ltd. 18149758185 18149758185 sales-cpd@caerulumpharma.com China 3467 58
Sichuan Wei Keqi Biological Technology Co., Ltd. 028-81700200 18116577057 3003855609@qq.com China 7787 56
Shanghai Lollane Biological Technology Co.,Ltd. 021-52996696,15000506266 15000506266 China 4621 55
Wellman Pharmaceutical Group Limited 027-83778875 15807197853 15807197853@163.com China 3935 58
esperamicin A1 Esperamicin A1 (BMY 28175) Carbamic acid, N-[(1R,4Z,8S,12S,13E)-8-[[4,6-dideoxy-2-O-[2,4-dideoxy-3-O-methyl-4-[(1-methylethyl)amino]-α-L-threo-pentopyranosyl]-4-[[(2,6-dideoxy-4-S-methyl-4-thio-β-D-ribo-hexopyranosyl)oxy]amino]-β-D-glucopyranosyl]oxy]-12-[[2,6-dideoxy-3-O-[4,5-dimethoxy-2-[(2-methoxy-1-oxo-2-propen-1-yl)amino... speramicin Eesperamicin A1 99674-26-7 C59H80N4O22S4