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6377-18-0 molecular structure
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3-{[(2S,3R,4S,5R,6R)-3-{[(2R,3R,4S,5S,6R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-8-hydroxy-15-methyl-11,18-dioxapentacyclo[10.6.2.02,7.09,19.016,20]icosa-1(19),2,4,6,8,12,14,16(20)-octaene-10,17-dione

ChemBase ID: 153416
Molecular Formular: C32H32O14
Molecular Mass: 640.58808
Monoisotopic Mass: 640.1792057
SMILES and InChIs

SMILES:
Cc1ccc2c3c1c(=O)oc1c3c(c(c3c1c(ccc3)O[C@H]1[C@@H]([C@H]([C@H]([C@H](O1)C)O)O)O[C@@H]1[C@@H]([C@H]([C@H]([C@H](O1)C)O)OC)O)O)c(=O)o2
Canonical SMILES:
CO[C@@H]1[C@@H](O)[C@@H](O[C@H]2[C@@H](O[C@@H]([C@@H]([C@@H]2O)O)C)Oc2cccc3c2c2oc(=O)c4c5c2c(c3O)c(=O)oc5ccc4C)O[C@@H]([C@@H]1O)C
InChI:
InChI=1S/C32H32O14/c1-10-8-9-15-18-16(10)29(38)45-26-17-13(23(35)20(19(18)26)30(39)43-15)6-5-7-14(17)44-32-28(24(36)21(33)11(2)42-32)46-31-25(37)27(40-4)22(34)12(3)41-31/h5-9,11-12,21-22,24-25,27-28,31-37H,1-4H3/t11-,12-,21+,22+,24+,25-,27+,28-,31-,32+/m1/s1
InChIKey:
PONPPNYZKHNPKZ-RYBWXQSLSA-N

Cite this record

CBID:153416 http://www.chembase.cn/molecule-153416.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
3-{[(2S,3R,4S,5R,6R)-3-{[(2R,3R,4S,5S,6R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-8-hydroxy-15-methyl-11,18-dioxapentacyclo[10.6.2.02,7.09,19.016,20]icosa-1(19),2,4,6,8,12,14,16(20)-octaene-10,17-dione
IUPAC Traditional name
3-{[(2S,3R,4S,5R,6R)-3-{[(2R,3R,4S,5S,6R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-8-hydroxy-15-methyl-11,18-dioxapentacyclo[10.6.2.02,7.09,19.016,20]icosa-1(19),2,4,6,8,12,14,16(20)-octaene-10,17-dione
Synonyms
Lambdamycin
Chartreusin from Streptomyces chartreusis
CAS Number
6377-18-0
MDL Number
MFCD00467138
PubChem SID
162247555
PubChem CID
5281394

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
C8448 external link Add to cart Please log in.
Data Source Data ID
PubChem 5281394 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 9.06726  H Acceptors 12 
H Donor LogD (pH = 5.5) 2.4738772 
LogD (pH = 7.4) 2.4648292  Log P 2.473994 
Molar Refractivity 154.3587 cm3 Polarizability 63.375305 Å3
Polar Surface Area 199.9 Å2 Rotatable Bonds
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
RTECS
FL7350000 expand Show data source
European Hazard Symbols
Harmful Harmful (Xn) expand Show data source
MSDS Link
Download expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
40 expand Show data source
Safety Statements
22-36/37/39-45 expand Show data source
GHS Pictograms
GHS08 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H351 expand Show data source
GHS Precautionary statements
P281 expand Show data source
Personal Protective Equipment
Eyeshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges expand Show data source
Storage Temperature
2-8°C expand Show data source
Empirical Formula (Hill Notation)
C32H32O14 expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - C8448 external link
Biochem/physiol Actions
Antitumor antibiotic which induces single-strand scission in DNA in the presence of reducing agents.1

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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