-
2-[(1S,2R,3R,7R,8S,9S,10R,12R,14Z,16S)-9-{[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde
-
ChemBase ID:
133863
-
Molecular Formular:
C31H51NO9
-
Molecular Mass:
581.73794
-
Monoisotopic Mass:
581.35638222
-
SMILES and InChIs
SMILES:
CC[C@@H]1[C@H]([C@H]2[C@@](O2)(/C=C\C(=O)[C@@H](C[C@@H]([C@@H]([C@H]([C@@H](CC(=O)O1)O)C)O[C@H]1[C@@H]([C@H](C[C@H](O1)C)N(C)C)O)CC=O)C)C)C
Canonical SMILES:
O=CC[C@H]1C[C@@H](C)C(=O)/C=C\[C@]2(C)O[C@H]2[C@@H]([C@H](OC(=O)C[C@H]([C@@H]([C@H]1O[C@@H]1O[C@H](C)C[C@@H]([C@H]1O)N(C)C)C)O)CC)C
InChI:
InChI=1S/C31H51NO9/c1-9-25-20(5)29-31(6,41-29)12-10-23(34)17(2)14-21(11-13-33)28(19(4)24(35)16-26(36)39-25)40-30-27(37)22(32(7)8)15-18(3)38-30/h10,12-13,17-22,24-25,27-30,35,37H,9,11,14-16H2,1-8H3/b12-10-/t17-,18-,19+,20-,21+,22+,24-,25-,27-,28-,29+,30+,31+/m1/s1
InChIKey:
IUPCWCLVECYZRV-MCECKBPDSA-N
-
Cite this record
CBID:133863 http://www.chembase.cn/molecule-133863.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
|
2-[(1S,2R,3R,7R,8S,9S,10R,12R,14Z,16S)-9-{[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde
|
|
|
IUPAC Traditional name
|
2-[(1S,2R,3R,7R,8S,9S,10R,12R,14Z,16S)-9-{[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde
|
|
|
Synonyms
|
Juvenimicin A3
|
Rosaramicin
|
Rosamicin
|
|
|
CAS Number
|
|
EC Number
|
|
MDL Number
|
|
Beilstein Number
|
|
PubChem SID
|
|
PubChem CID
|
|
DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
Acid pKa
|
12.79468
|
H Acceptors
|
9
|
H Donor
|
2
|
LogD (pH = 5.5)
|
0.51455915
|
LogD (pH = 7.4)
|
2.2145782
|
Log P
|
2.6783903
|
Molar Refractivity
|
153.4187 cm3
|
Polarizability
|
61.214565 Å3
|
Polar Surface Area
|
135.13 Å2
|
Rotatable Bonds
|
6
|
Lipinski's Rule of Five
|
false
|
DETAILS
DETAILS
Sigma Aldrich
Sigma Aldrich -
R2636
|
Biochem/physiol Actions Macrolide antibiotic similar to erythromycin, and with a similar spectrum of bactericidal activity.1 Against a wide variety of anaerobes, rosamicin is at least as potent as, and in some cases more potent than, erythromycin.2 |
PATENTS
PATENTS
PubChem Patent
Google Patent