himastatin

Modify Date: 2024-01-11 16:15:30

himastatin Structure
himastatin structure
Common Name himastatin
CAS Number 126775-74-4 Molecular Weight 2971.356
Density N/A Boiling Point N/A
Molecular Formula C144H208N28O40 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of himastatin


Himastatin is a antitumor antibiotic produced by a strain of S. hygroscopicus sp. Himastatin is a dimeric cyclohexadepsipeptide containing piperazic acid and a unique central aromatic core[1].

 Names

Name (5E,5'E,8E,8'E,19E,19'E)-3,3',5,5',8,8',17b,17b',19,19'-Decahydroxy-10,10'-bis(1-hydroxyethyl)-7,7'-diisobutyl-21,21',24,24'-tetraisopropyl-2,2',3,3',4,4',4a,4a',7,7',10,10',17b,17b',18,18',18a,18a',21,21'-icosahydro-12aH,12a'H-16,16'-bipyridazino[6'',1'':15',16'][1,4,7,10,13,16]oxapentaazacyclooctadecino[7',6':1,5]pyrrolo[2,3-b]indole-11,11',22,22',25,25'(1H,1'H,13H,13'H,24H,24'H)-hexone-(7E,20E,23E,39E,52E,55E)-4,7,17,20,23,36,39,49,52,55-decahydroxy-25,57-bis(1-hydroxyethyl)-22,54-diisobutyl-9,12,41,44-tetraisopropyl-11,43-dioxa-8,14,15,21,24,27,29,40,46,47,53,56,59,61-tetradecaazadecacyclo[31.31.0.03,62.04,60.06,59.014,19.027,38.028,36.030,35.046,51]tetrahexaconta-1(64),2,7,20,23,30,32,34,39,52,55,62-dodecaene-10,13,26,42,45,58-hexone (1:1)

 himastatin Biological Activity

Description Himastatin is a antitumor antibiotic produced by a strain of S. hygroscopicus sp. Himastatin is a dimeric cyclohexadepsipeptide containing piperazic acid and a unique central aromatic core[1].
Related Catalog
References

[1]. Leet JE, Schroeder DR, Krishnan BS, Matson JA. Himastatin, a new antitumor antibiotic from Streptomyces hygroscopicus. II. Isolation and characterization. J Antibiot (Tokyo). 1990;43(8):961-966.

 Chemical & Physical Properties

Molecular Formula C144H208N28O40
Molecular Weight 2971.356
Exact Mass 2969.510254
InChIKey OZPNLJQULOIOGU-IEGPOQBUSA-N
SMILES CC(C)CC1NC(=O)C2CC(O)CNN2C(=O)C(C(C)C)OC(=O)C(C(C)C)NC(=O)C2CC3(O)c4cc(-c5ccc6c(c5)C5(O)CC7C(=O)NC(C(C)C)C(=O)OC(C(C)C)C(=O)N8NCC(O)CC8C(=O)NC(CC(C)C)C(=O)NC(C(C)O)C(=O)N7C5N6)ccc4NC3N2C(=O)C(C(C)O)NC1=O
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