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Technology Process of Quartromicin A1

Quartromicin A1

Base Information
  • Chemical Name:Quartromicin A1
  • CAS No.:136765-19-0
  • Molecular Formula:C77H98O30-4
  • Molecular Weight:1503.5862
  • Hs Code.:
  • Metabolomics Workbench ID:102834
Quartromicin A1

Synonyms:Quartromicin A1;BU-3889V A1;136765-19-0;4a,7:14a,17:26a,29:36a,39-Tetrametheno-6H,16H,28H,38H-tetrabenzo(b,j,t,b1)(1,9,19,27)tetraoxacyclohexatriacontin-12,34-dicarboxaldehyde, 2,24-bis((alpha-D-galactopyranosyloxy)methyl)-3,4,8,10a,13,14,18,22a,25,26,30,32a,35,36,40,44a-hexadecahydro-45,46,47,48-tetrahydroxy-3,10a,13,19,22a,25,32a,35,41,44a-decamethyl-6,8,16,18,28,30,38,40-octaoxo-;4a,7:14a,17:26a,29:36a,39-Tetrametheno-6H,16H,28H,38H-tetrabenzo[b,j,t,b1][1,9,19,27]tetraoxacyclohexatriacontin-12,34-dicarboxaldehyde, 2,24-bis[(.alpha.-D-galactopyranosyloxy)methyl]-3,4,8,10a,13,14,18,22a,25,26,30,32a,35,36,40,44a-hexadecahydro-45,46,47,48-tetrahydroxy-3,10a,13,19,22a,25,32a,35,41,44a-decamethyl-6,8,16,18,28,30,38,40-octaoxo-;octahydroxy-nonamethyl-tetraoxo-bis[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxymethyl][?]dicarbaldehyde

Suppliers and Price of Quartromicin A1
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Quartromicin A1
Chemical Property:
  • PKA:4.20±1.00(Predicted) 
  • Density:1.54±0.1 g/cm3(Predicted) 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:12
  • Hydrogen Bond Acceptor Count:30
  • Rotatable Bond Count:10
  • Exact Mass:1502.61429170
  • Heavy Atom Count:107
  • Complexity:3760
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1CC23C(C=CC=C(C(C4C(OC5(C4=O)CC(C(=CC5(C=CC(C6C(OC7(C6=O)CC(C(=CC7(C=CC=C(C(C8C(OC9(C8=O)CC(C(=CC9(C=CC(C(C2=O)C(O3)[O-])O)C)C=O)C)[O-])O)C)C)COC2C(C(C(C(O2)CO)O)O)O)C)[O-])O)C)C=O)C)[O-])O)C)C=C1COC1C(C(C(C(O1)CO)O)O)O
  • Isomeric SMILES:CC1CC23C(/C=C/C=C(/C(C4C(OC5(C4=O)CC(C(=CC5(/C=C/C(C6C(OC7(C6=O)CC(C(=CC7(/C=C/C=C(/C(C8C(OC9(C8=O)CC(C(=CC9(/C=C/C(C(C2=O)C(O3)[O-])O)C)C=O)C)[O-])O)\C)C)CO[C@@H]2[C@@H]([C@H]([C@H]([C@H](O2)CO)O)O)O)C)[O-])O)C)C=O)C)[O-])O)\C)C=C1CO[C@@H]1[C@@H]([C@H]([C@H]([C@H](O1)CO)O)O)O
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