Skip Navigation
ChemIDplus A TOXNET DATABASE LiteBrowseAdvanced

Substance Name: Racemomycin E
RN: 3484-68-2
InChIKey: SFBVRPSSMVXTDR-PTESPJIQSA-N

Classification Code

  • Natural Product

Molecular Formula

  • C43-H82-N16-O12

Molecular Weight

  • 1015.22
 
* denotes mobile formatted website

Links to Resources

NLM Resources (File Locators)

Other Resources (Internet Locators)


Search for this InChIKey on the Web

Names and Synonyms

Results Name

  • Racemomycin E

Synonyms

  • 4H-Imidazo(4,5-c)pyridin-4-one, 2-((4-O-(aminocarbonyl)-2-deoxy-2-((3,10,17,24,31,34-hexaamino-1,8,15,22,29-pentaoxo-7,14,21,28-tetraazatetratriacont-1-yl)amino)-beta-D-gulopyranosyl)amino)-1,3a,5,6,7,7a-hexahydro-7-hydroxy-, (3aS-(2(3R*,10R*,17R*,24R*,31R*),3aalpha,7alpha,7abeta))-
  • A 53930C
  • Racemomycin E
  • Streptothricin B

Systematic Names

  • 4H-Imidazo(4,5-c)pyridin-4-one, 2-((2-(3-amino-6-(3-amino-6-(3-amino-6-(3-amino-6-(3,6-diaminohexanamido)hexanamido)hexanamido)hexanamido)hexanamido)-2-deoxy-beta-D-gulopyranosyl)amino)-3,3a,5,6,7,7a-hexahydro-7-hydroxy-, 6'-carbamate
  • 4H-Imidazo(4,5-c)pyridin-4-one, 2-((4-O-(aminocarbonyl)-2-deoxy-2-(((3S,10S,17S,24S,31S)-3,10,17,24,31,34-hexaamino-1,8,15,22,29-pentaoxo-7,14,21,28-tetraazatetratriacont-1-yl)amino)-beta-D-gulopyranosyl)amino)-1,3a,5,6,7,7a-hexahydro-7-hydroxy-, (3aS,7R,7aS)-

Registry Numbers

CAS Registry Number

  • 3484-68-2

System Generated Number

  • 0003484682

Structure Descriptors

InChI

1S/C43H82N16O12/c44-11-1-6-23(45)16-30(62)51-12-2-7-24(46)17-31(63)52-13-3-8-25(47)18-32(64)53-14-4-9-26(48)19-33(65)54-15-5-10-27(49)20-34(66)56-37-38(67)39(71-42(50)69)29(22-60)70-41(37)59-43-57-35-28(61)21-55-40(68)36(35)58-43/h23-29,35-39,41,60-61,67H,1-22,44-49H2,(H2,50,69)(H,51,62)(H,52,63)(H,53,64)(H,54,65)(H,55,68)(H,56,66)(H2,57,58,59)/t23-,24-,25-,26-,27-,28+,29+,35+,36-,37+,38-,39-,41+/m0/s1

InChIKey

SFBVRPSSMVXTDR-PTESPJIQSA-N

Smiles

N[C@@H](CCCN)CC(NCCC[C@@H](CC(NCCC[C@H](N)CC(NCCC[C@@H](CC(NCCC[C@@H](CC(N[C@H]1[C@H](NC=2N[C@@H]3[C@@H](CNC([C@@H]3N2)=O)O)O[C@@H]([C@@H]([C@H]1O)OC(=O)N)CO)=O)N)=O)N)=O)=O)N)=O

Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 subcutaneous 55800mg/kg (55800mg/kg)   Antibiotiki. Vol. 14, Pg. 48, 1969.
mouse LDLo intravenous 208ug/kg (0.208mg/kg)   Journal of Antibiotics. Vol. 3, Pg. 232, 1950.