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1165-39-5 molecular structure
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(3S,7R)-11-methoxy-6,8,16,20-tetraoxapentacyclo[10.8.0.02,9.03,7.013,18]icosa-1,4,9,11,13(18)-pentaene-17,19-dione

ChemBase ID: 159586
Molecular Formular: C17H12O7
Molecular Mass: 328.27298
Monoisotopic Mass: 328.05830272
SMILES and InChIs

SMILES:
c12c(cc(c3c1oc(=O)c1c3CCOC1=O)OC)O[C@@H]1[C@H]2C=CO1
Canonical SMILES:
COc1cc2O[C@@H]3[C@H](c2c2c1c1CCOC(=O)c1c(=O)o2)C=CO3
InChI:
InChI=1S/C17H12O7/c1-20-9-6-10-12(8-3-5-22-17(8)23-10)14-11(9)7-2-4-21-15(18)13(7)16(19)24-14/h3,5-6,8,17H,2,4H2,1H3/t8-,17+/m0/s1
InChIKey:
XWIYFDMXXLINPU-WNWIJWBNSA-N

Cite this record

CBID:159586 http://www.chembase.cn/molecule-159586.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(3S,7R)-11-methoxy-6,8,16,20-tetraoxapentacyclo[10.8.0.02,9.03,7.013,18]icosa-1,4,9,11,13(18)-pentaene-17,19-dione
IUPAC Traditional name
(3S,7R)-11-methoxy-6,8,16,20-tetraoxapentacyclo[10.8.0.02,9.03,7.013,18]icosa-1,4,9,11,13(18)-pentaene-17,19-dione
Synonyms
(7aR,10aS)-3,4,7a,10a-Tetrahydro-5-methoxy-1H,12H-furo[3’,2’:4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione
Aflatoxin G1
CAS Number
1165-39-5
PubChem SID
162253721
PubChem CID
2724361

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
TRC A357480 external link Add to cart
PubChem 2724361 external link
Data Source Data ID Price
TRC
A357480 external link Add to cart Please log in.
Data Source Data ID
PubChem 2724361 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
H Acceptors H Donor
LogD (pH = 5.5) 1.3682086  LogD (pH = 7.4) 1.3682086 
Log P 1.3682086  Molar Refractivity 79.8478 cm3
Polarizability 30.937191 Å3 Polar Surface Area 80.29 Å2
Rotatable Bonds Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
Chloroform expand Show data source
Apperance
Light Yellow Solid expand Show data source
Melting Point
240-244°C expand Show data source
Storage Condition
-20°C Freezer, Under Inert Atmosphere expand Show data source
MSDS Link
Download expand Show data source
Certificate of Analysis
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DETAILS

DETAILS

TRC TRC
Toronto Research Chemicals - A357480 external link
Aflatoxins B1, B2, G1, G2 as secondary metabolites of fungal species such as Aspergillus flavus or Aspergillus parasiticus growing on a variety of foods (peanuts, nuts, spices, cereals). Aflatoxins are a group of very carcinogenic mycotoxins with hepatot

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Cifford, R., et al.: Nature, 209, 312 (1966)
  • • Wogan, et al.: Food Cosmet. Toxicol., 12, 681 (1966)
  • • Sinz, M.W., et al.: J. Toxicol. Toxin Rev., 10, 87 (1966)
  • • Shantha, T., et al.: Nat. Toxins, 7, 175 (1966)
  • • Kim, J., et al.: J. Food Prod., 63, 1295 (2000)
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PATENTS

PATENTS

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INTERNET

INTERNET

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