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1405-37-4 molecular structure
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(2S)-2,5-diamino-N-{[(2S,5R,8Z,11S,15R)-15-amino-8-[(carbamoylamino)methylidene]-2-(hydroxymethyl)-11-(2-imino-1,3-diazinan-4-yl)-3,6,9,12,16-pentaoxo-1,4,7,10,13-pentaazacyclohexadecan-5-yl]methyl}pentanamide; sulfuric acid

ChemBase ID: 132489
Molecular Formular: C24H44N14O12S
Molecular Mass: 752.75776
Monoisotopic Mass: 752.29838392
SMILES and InChIs

SMILES:
C1CNC(=N)NC1[C@H]1C(=O)NC[C@H](C(=O)N[C@H](C(=O)N[C@@H](C(=O)N/C(=C\NC(=O)N)/C(=O)N1)CNC(=O)[C@H](CCCN)N)CO)N.OS(=O)(=O)O
Canonical SMILES:
OS(=O)(=O)O.NCCC[C@@H](C(=O)NC[C@H]1NC(=O)[C@H](CO)NC(=O)[C@H](N)CNC(=O)[C@@H](NC(=O)/C(=C/NC(=O)N)/NC1=O)C1CCNC(=N)N1)N
InChI:
InChI=1S/C24H42N14O8.H2O4S/c25-4-1-2-10(26)17(40)32-7-13-19(42)34-14(8-33-24(29)46)20(43)38-16(12-3-5-30-23(28)37-12)22(45)31-6-11(27)18(41)36-15(9-39)21(44)35-13;1-5(2,3)4/h8,10-13,15-16,39H,1-7,9,25-27H2,(H,31,45)(H,32,40)(H,34,42)(H,35,44)(H,36,41)(H,38,43)(H3,28,30,37)(H3,29,33,46);(H2,1,2,3,4)/b14-8-;/t10-,11+,12?,13+,15-,16-;/m0./s1
InChIKey:
LFFNIXQXRKNZCE-UBBQZPMLSA-N

Cite this record

CBID:132489 http://www.chembase.cn/molecule-132489.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(2S)-2,5-diamino-N-{[(2S,5R,8Z,11S,15R)-15-amino-8-[(carbamoylamino)methylidene]-2-(hydroxymethyl)-11-(2-imino-1,3-diazinan-4-yl)-3,6,9,12,16-pentaoxo-1,4,7,10,13-pentaazacyclohexadecan-5-yl]methyl}pentanamide; sulfuric acid
IUPAC Traditional name
(2S)-2,5-diamino-N-{[(2S,5R,8Z,11S,15R)-15-amino-8-[(carbamoylamino)methylidene]-2-(hydroxymethyl)-11-(2-imino-1,3-diazinan-4-yl)-3,6,9,12,16-pentaoxo-1,4,7,10,13-pentaazacyclohexadecan-5-yl]methyl}pentanamide; sulfuric acid
Synonyms
Capreomycin sulfate from Streptomyces capreolus
CAS Number
1405-37-4
EC Number
215-776-8
MDL Number
MFCD00079032
PubChem SID
24892668
162226766
PubChem CID
16219119

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
C4142 external link Add to cart Please log in.
Data Source Data ID
PubChem 16219119 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 10.393468  H Acceptors 14 
H Donor 15  LogD (pH = 5.5) -19.886066 
LogD (pH = 7.4) -16.16658  Log P -11.034652 
Molar Refractivity 167.8734 cm3 Polarizability 61.442654 Å3
Polar Surface Area 375.92 Å2 Rotatable Bonds
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Safety Information Bioassay(PubChem)
RTECS
EX8930000 expand Show data source
European Hazard Symbols
Toxic Toxic (T) expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
61-20/21/22 expand Show data source
Safety Statements
53-22-36/37/39-45 expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS08 expand Show data source
GHS Signal Word
Danger expand Show data source
GHS Hazard statements
H302-H312-H332-H360 expand Show data source
GHS Precautionary statements
P201-P280-P308 + P313 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
-20°C expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - C4142 external link
Application
Capreomycin is a cyclic peptide antibiotic that is often grouped with aminoglycosides. It is a second line antibiotic and is used to study multidrug-resistant tuberculosis 1,2.
Capreomycin sulfate is used to study bacterial ribosomal subunit interactions and translocation processes during protein synthesis.
Biochem/physiol Actions
Capreomycin sulfate binds across the ribosomal interface involving 23S rRNA helix 69 (H69) and 16S rRNA helix 44 (h44) 3.

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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