IMPPAT Phytochemical information: 
Kinetin

Kinetin
Summary

SMILES: c1coc(c1)CNc1ncnc2c1[nH]cn2
InChI: InChI=1S/C10H9N5O/c1-2-7(16-3-1)4-11-9-8-10(13-5-12-8)15-6-14-9/h1-3,5-6H,4H2,(H2,11,12,13,14,15)
InChIKey: QANMHLXAZMSUEX-UHFFFAOYSA-N
DeepSMILES: ccocc5)CNcncncc6[nH]cn5
Scaffold Graph/Node/Bond level: c1coc(CNc2ncnc3nc[nH]c23)c1
Scaffold Graph/Node level: C1COC(CNC2NCNC3NCNC32)C1
Scaffold Graph level: C1CCC(CCC2CCCC3CCCC32)C1
Functional groups: coc; cNC; cnc; c[nH]c
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Organoheterocyclic compounds
ClassyFire Class: Imidazopyrimidines
ClassyFire Subclass: Purines and purine derivatives
NP Classifier Biosynthetic pathway: Alkaloids
NP Classifier Superclass: Pseudoalkaloids
NP Classifier Class: Purine alkaloids
Synonymous chemical names:
kinetin, cytokinin
External chemical identifiers:
CID:CID_3830; ChEMBL:CHEMBL228792; ChEBI:CHEBI:27407; ZINC:ZINC000000001601; FDASRS:P39Y9652YJ; SureChEMBL:SCHEMBL15705; MolPort-006-111-624
Chemical structure download


Kinetin
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 215.22
Log P RDKit 1.56
Topological polar surface area (Å2) RDKit 79.63
Number of hydrogen bond acceptors RDKit 5
Number of hydrogen bond donors RDKit 2
Number of carbon atoms RDKit 10
Number of heavy atoms RDKit 16
Number of heteroatoms RDKit 6
Number of nitrogen atoms RDKit 5
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 0
Stereochemical complexity RDKit 0
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 9
Number of sp3 hybridized carbon atoms RDKit 1
Shape complexity RDKit 0.1
Number of rotatable bonds RDKit 3
Number of aliphatic carbocycles RDKit 0
Number of aliphatic heterocycles RDKit 0
Number of aliphatic rings RDKit 0
Number of aromatic carbocycles RDKit 0
Number of aromatic heterocycles RDKit 3
Number of aromatic rings RDKit 3
Total number of rings RDKit 3
Number of saturated carbocycles RDKit 0
Number of saturated heterocycles RDKit 0
Number of saturated rings RDKit 0
Number of Smallest Set of Smallest Rings (SSSR) RDKit 3


Kinetin
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 0
Lipinski’s rule of 5 filter RDKit Passed
Number of Ghose filter violations RDKit 0
Ghose filter RDKit Passed
Veber filter RDKit Good
Pfizer 3/75 filter RDKit Good
GSK 4/400 filter RDKit Good
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.692593


Kinetin
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Soluble
Solubility class [Silicos-IT] SwissADME Moderately soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME High
Log Kp (Skin permeation, cm/s) SwissADME -6.90
Number of PAINS structural alerts SwissADME 0
Number of Brenk structural alerts SwissADME 0
CYP1A2 inhibitor SwissADME Yes
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME No
CYP2D6 inhibitor SwissADME Yes
CYP3A4 inhibitor SwissADME Yes
P-glycoprotein substrate SwissADME Yes


Kinetin
Human target proteins
Protein identifierHGNC symbolCombined score from STITCH database
ENSP00000343925ESR2800
ENSP00000363779IKBKAP950
ENSP00000426909GNB2L1800
ENSP00000350387HYAL2953
ENSP00000345849SPAM1940
ENSP00000223026HYAL4712
ENSP00000206249ESR1800
The human target proteins were predicted using STITCH, a database of Chemical-Protein interaction networks.