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37517-28-5(anhydrous) molecular structure
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(2S)-4-amino-N-[(1R,2S,3S,4R,5S)-5-amino-2-{[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4-{[(2R,3R,4S,5S,6R)-6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-hydroxycyclohexyl]-2-hydroxybutanamide hydrate

ChemBase ID: 132448
Molecular Formular: C22H45N5O14
Molecular Mass: 603.6178
Monoisotopic Mass: 603.29630115
SMILES and InChIs

SMILES:
C1[C@@H]([C@H]([C@@H]([C@H]([C@@H]1NC(=O)[C@H](CCN)O)O[C@@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)N)O)O)O[C@@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CN)O)O)O)N.O
Canonical SMILES:
NCC[C@@H](C(=O)N[C@@H]1C[C@H](N)[C@H]([C@@H]([C@H]1O[C@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)N)O)O)O[C@H]1O[C@H](CN)[C@H]([C@@H]([C@H]1O)O)O)O.O
InChI:
InChI=1S/C22H43N5O13.H2O/c23-2-1-8(29)20(36)27-7-3-6(25)18(39-22-16(34)15(33)13(31)9(4-24)37-22)17(35)19(7)40-21-14(32)11(26)12(30)10(5-28)38-21;/h6-19,21-22,28-35H,1-5,23-26H2,(H,27,36);1H2/t6-,7+,8-,9+,10+,11-,12+,13+,14+,15-,16+,17-,18+,19-,21+,22+;/m0./s1
InChIKey:
DTSOZYYWEZJFSS-XTHCGPPUSA-N

Cite this record

CBID:132448 http://www.chembase.cn/molecule-132448.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(2S)-4-amino-N-[(1R,2S,3S,4R,5S)-5-amino-2-{[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4-{[(2R,3R,4S,5S,6R)-6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-hydroxycyclohexyl]-2-hydroxybutanamide hydrate
IUPAC Traditional name
amikacin hydrate
Synonyms
N1-[(S)-4-Amino-2-hydroxybutyryl]kanamycin A
Amikacin hydrate
CAS Number
37517-28-5(anhydrous)
EC Number
253-538-5
MDL Number
MFCD11045969
Beilstein Number
1445422
PubChem SID
162226725
24890796
PubChem CID
16218899

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
A3650 external link Add to cart Please log in.
Data Source Data ID
PubChem 16218899 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 12.104234  H Acceptors 17 
H Donor 13  LogD (pH = 5.5) -20.16644 
LogD (pH = 7.4) -15.099279  Log P -8.584383 
Molar Refractivity 129.841 cm3 Polarizability 54.552784 Å3
Polar Surface Area 331.94 Å2 Rotatable Bonds 10 
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Safety Information Bioassay(PubChem)
RTECS
WK1955000 expand Show data source
German water hazard class
2 expand Show data source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source
Storage Temperature
2-8°C expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - A3650 external link
Application
Amikacin hydrate is used in antimicrobial susceptibility studies of organisms such as Mycobacterium tuberculosis1and Ehrlichia phagocytophila.2
Biochem/physiol Actions
Amikacin prevents bacterial protein synthesis by binding to the 30S ribosome subunit and inducing mRNA misreading.

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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