(Q105386341)

English

ZYQCEUUNWXOPRE-UPKPQOFHSA-N

chemical compound

In more languages

Statements

type of chemical entity

0 references

tryptamine alkaloid

0 references

1,329.141779948 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₆₁H₄₉Cl₆N₇O₁₅

0 references

canonical SMILES

CN(C(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(Cc1c[nH]c2ccccc12)NC(=O)C(=O)c1cc(Cl)c(O)c(Cl)c1)c1cc(Cl)c(O)c(Cl)c1)c1ccc(O)cc1)c1cc(Cl)c(O)c(Cl)c1)C(Cc1ccc(O)cc1)C(=O)NC(C(=O)O)c1ccc(O)cc1

0 references

isomeric SMILES

CN(C(=O)[C@H](NC(=O)[C@H](NC(=O)[C@@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(=O)c1cc(Cl)c(O)c(Cl)c1)c1cc(Cl)c(O)c(Cl)c1)c1ccc(O)cc1)c1cc(Cl)c(O)c(Cl)c1)[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](C(=O)O)c1ccc(O)cc1

0 references

Streptomyces lividans

1 reference

Generation of New Complestatin Analogues by Heterologous Expression of the Complestatin Biosynthetic Gene Cluster from Streptomyces chartreusis AN1542.

Streptomyces anthocyanicus

1 reference

Generation of New Complestatin Analogues by Heterologous Expression of the Complestatin Biosynthetic Gene Cluster from Streptomyces chartreusis AN1542.

Identifiers

InChI=1S/C61H49Cl6N7O15/c1-74(46(18-27-6-12-34(75)13-7-27)56(83)73-50(61(88)89)29-10-16-36(77)17-11-29)60(87)49(31-21-40(64)53(80)41(65)22-31)72-57(84)47(28-8-14-35(76)15-9-28)71-58(85)48(30-19-38(62)52(79)39(63)20-30)70-55(82)45(25-33-26-68-44-5-3-2-4-37(33)44)69-59(86)51(78)32-23-42(66)54(81)43(67)24-32/h2-17,19-24,26,45-50,68,75-77,79-81H,18,25H2,1H3,(H,69,86)(H,70,82)(H,71,85)(H,72,84)(H,73,83)(H,88,89)/t45-,46-,47+,48-,49+,50+/m0/s1

0 references

ZYQCEUUNWXOPRE-UPKPQOFHSA-N

0 references

1 reference

15 September 2022

1 reference

15 September 2022

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q105386341&oldid=2011129384"