Kanamycin

Details

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Internal ID a3f8cf43-8b1e-4f1f-96fa-c435552cd9fb
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > 2-deoxystreptamine aminoglycosides > 4,6-disubstituted 2-deoxystreptamines
IUPAC Name (2R,3S,4S,5R,6R)-2-(aminomethyl)-6-[(1R,2R,3S,4R,6S)-4,6-diamino-3-[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxyoxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H36N4O11/c19-2-6-10(25)12(27)13(28)18(30-6)33-16-5(21)1-4(20)15(14(16)29)32-17-11(26)8(22)9(24)7(3-23)31-17/h4-18,23-29H,1-3,19-22H2/t4-,5+,6-,7-,8+,9-,10-,11-,12+,13-,14-,15+,16-,17-,18-/m1/s1
InChI Key SBUJHOSQTJFQJX-NOAMYHISSA-N
Popularity 42,322 references in papers

Physical and Chemical Properties

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Molecular Formula C18H36N4O11
Molecular Weight 484.50 g/mol
Exact Mass 484.23805798 g/mol
Topological Polar Surface Area (TPSA) 283.00 Ų
XlogP -6.90

Synonyms

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Kanamicina
Kanamycine
Kanamycinum
8063-07-8
Kanamycins
(2R,3S,4S,5R,6R)-2-(aminomethyl)-6-[(1R,2R,3S,4R,6S)-4,6-diamino-3-[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxyoxane-3,4,5-triol
D-Streptamine, O-3-amino-3-deoxy-alpha-D-glucopyranosyl-(1-6)-O-(6-amino-6-deoxy-alpha-D-glucopyranosyl-(1-4))-2-deoxy-
(2R,3S,4S,5R,6R)-2-(aminomethyl)-6-{[(1R,2R,3S,4R,6S)-4,6-diamino-3-{[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexyl]oxy}oxane-3,4,5-triol
Kanamycin Complex
(2R,3S,4S,5R,6R)-2-(aminomethyl)-6-(((1R,2R,3S,4R,6S)-4,6-diamino-3-(((2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy)-2-hydroxycyclohexyl)oxy)oxane-3,4,5-triol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Kanamycin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3137262 O60341 LSD1/CoREST complex 97.33% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.25% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 92.72% 95.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.45% 96.09%
CHEMBL3589 P55263 Adenosine kinase 91.51% 98.05%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 86.66% 95.58%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.52% 86.92%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.84% 96.21%
CHEMBL4101 P17612 cAMP-dependent protein kinase alpha-catalytic subunit 81.95% 82.86%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.89% 96.61%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.34% 95.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Elateriospermum tapos

Cross-Links

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PubChem 6032
LOTUS LTS0046726
wikiData Q27094615