Skip Navigation
ChemIDplus A TOXNET DATABASE LiteBrowseAdvanced

Substance Name: Luteoskyrin
RN: 21884-44-6
InChIKey: KXNUPFFSGSRABD-UHFFFAOYSA-N

Note

  • Mycotoxin from Penicillium islandicum; pollutant of stored rice.

Molecular Formula

  • C30-H22-O12

Molecular Weight

  • 574.492
 

Classification Codes

Classification Codes

  • Mutation Data
  • Natural Product
  • Tumor Data

Superlist Classification Code

  • Overall Carcinogenic Evaluation: Group 3
* denotes mobile formatted website

Links to Resources

NLM Resources (File Locators)

Regulatory Agencies (Superlist Locators)

Other Resources (Internet Locators)


Search for this InChIKey on the Web

Names and Synonyms

Name of Substance

  • Luteoskyrin

Synonyms

  • (1beta,1'beta,3beta,3'beta)-8,8'-Dihydroxy-rugulosin
  • 2,2',3,3'-Tetrahydro-2,2',4,4',5,5',8,8'-octahydroxy-7,7'-dimethyl-(1,1'-bianthracene)-9,9',10,10'-tetrone
  • 2,2',4,4'5,5',8,8'-Octahydroxy-2,2',3,3'-tetrahydro-7,7'-dimethyl-1,1'-bianthraquinone
  • 5H,6H-6,13a,5a,14-(1,2,3,4)Butanetetraylcycloocta(1,2-b:5,6-b')dinaphthalene-5,8,13,16(14H)-tetrone, 1,4,7,9,12,15,17,20-octahydroxy-3,11-dimethyl-
  • 8,8'-Dihydroxy-rugulosin
  • CCRIS 365
  • EINECS 244-631-1
  • Flavomycelin
  • HSDB 3508
  • Luteoskyrin
  • NSC 160879
  • RUGULOSIN, 8,8'-DEHYDROXY-
  • Rugulosin, 8,8'-dihydroxy-
  • Rugulosin, 8,8'-dihydroxy-, (1S,1'S,2R,2'R,3S,3'S,9aR,9'aR)-

Systematic Names

  • 5H,6H-6,13a,5a,14-(1,2,3,4)Butanetetraylcycloocta(1,2-b:5,6-b')dinaphthalene-5,8,13,16(14H)-tetrone, 1,4,7,9,12,15,17,20-octahydroxy-3,11-dimethyl- (8CI)
  • 5H,6H-6,5a,13a,14-(1,2,3,4)Butanetetraylcycloocta(1,2-b:5,6-b')dinaphthalene-5,8,13,16(14H)-tetrone, 1,4,7,9,12,15,17,20-octahydroxy-3,11-dimethyl-, (5aR- (5aR*,6S*,13aR*,14S*,17R*,18S*,19S*,20R*))-
  • Luteoskyrin
  • Rugulosin, 8,8'-dihydroxy-, (1S,1'S,2R,2'R,3S,3'S,9aR,9'aR)-

Superlist Name

  • Luteoskyrin

Registry Numbers

CAS Registry Number

  • 21884-44-6

Other Registry Numbers

  • 10088-79-6
  • 1402-11-5
  • 27618-64-0

System Generated Number

  • 0021884446

Structure Descriptors

InChI

1S/C30H22O12/c1-5-3-7(31)9-11(19(5)33)27(41)29-13-14-24(38)17(29)26(40)16-22(36)10-8(32)4-6(2)20(34)12(10)28(42)30(14,16)18(23(13)37)25(39)15(29)21(9)35/h3-4,13-14,17-18,23-24,31-34,37-40H,1-2H3

InChIKey

KXNUPFFSGSRABD-UHFFFAOYSA-N

Smiles

C=12[C@@]3([C@@H]4[C@@H]5[C@@]6(C(c7c(c(C)cc(c7C(C6=C([C@@H]3[C@@H]5O)O)=O)O)O)=O)[C@@H]([C@@H]4O)C1O)C(c1c(c(C)cc(c1C2=O)O)O)=O

Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 41mg/kg (41mg/kg)   Japanese Journal of Experimental Medicine. Vol. 41, Pg. 177, 1971.
mouse LD50 intravenous 6650ug/kg (6.65mg/kg) LIVER: LIVER FUNCTION TESTS IMPAIRED

LIVER: "HEPATITIS (HEPATOCELLULAR NECROSIS), ZONAL"

LIVER: FATTY LIVER DEGERATION
Food and Cosmetics Toxicology. Vol. 10, Pg. 193, 1972.
mouse LD50 oral 220mg/kg (220mg/kg)   Alimentation et la Vie. Vol. 50, Pg. 77, 1962.
mouse LD50 subcutaneous 146mg/kg (146mg/kg)   Japanese Journal of Experimental Medicine. Vol. 42, Pg. 91, 1972.