-
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
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
|
|
MDL Number
|
|
PubChem SID
|
|
PubChem CID
|
|
DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
Acid pKa
|
9.06726
|
H Acceptors
|
12
|
H Donor
|
5
|
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
|
5
|
Lipinski's Rule of Five
|
false
|
DETAILS
DETAILS
Sigma Aldrich
Sigma Aldrich -
C8448
|
Biochem/physiol Actions Antitumor antibiotic which induces single-strand scission in DNA in the presence of reducing agents.1 |
PATENTS
PATENTS
PubChem Patent
Google Patent