Kazinol J

Details

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Internal ID 41c9df90-5828-4a4e-a6e1-1059f49e0b46
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Cinnamylphenols
IUPAC Name 5-[3-(4-hydroxy-2-methoxyphenyl)propyl]-3,4-bis(3-methylbut-2-enyl)benzene-1,2-diol
SMILES (Canonical) CC(=CCC1=C(C(=C(C=C1CCCC2=C(C=C(C=C2)O)OC)O)O)CC=C(C)C)C
SMILES (Isomeric) CC(=CCC1=C(C(=C(C=C1CCCC2=C(C=C(C=C2)O)OC)O)O)CC=C(C)C)C
InChI InChI=1S/C26H34O4/c1-17(2)9-13-22-20(15-24(28)26(29)23(22)14-10-18(3)4)8-6-7-19-11-12-21(27)16-25(19)30-5/h9-12,15-16,27-29H,6-8,13-14H2,1-5H3
InChI Key BUWRWZUUCOLPSX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H34O4
Molecular Weight 410.50 g/mol
Exact Mass 410.24570956 g/mol
Topological Polar Surface Area (TPSA) 69.90 Ų
XlogP 7.40
Atomic LogP (AlogP) 6.00
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 9

Synonyms

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CHEMBL464845

2D Structure

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2D Structure of Kazinol J

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9747 97.47%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8805 88.05%
OATP2B1 inhibitior - 0.8497 84.97%
OATP1B1 inhibitior + 0.8425 84.25%
OATP1B3 inhibitior + 0.9163 91.63%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.9562 95.62%
P-glycoprotein inhibitior + 0.8535 85.35%
P-glycoprotein substrate - 0.5185 51.85%
CYP3A4 substrate + 0.5311 53.11%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate + 0.3868 38.68%
CYP3A4 inhibition - 0.7074 70.74%
CYP2C9 inhibition + 0.6222 62.22%
CYP2C19 inhibition + 0.7487 74.87%
CYP2D6 inhibition - 0.7278 72.78%
CYP1A2 inhibition + 0.7014 70.14%
CYP2C8 inhibition + 0.7791 77.91%
CYP inhibitory promiscuity + 0.5467 54.67%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8386 83.86%
Carcinogenicity (trinary) Non-required 0.7291 72.91%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.6661 66.61%
Skin irritation - 0.7819 78.19%
Skin corrosion - 0.9204 92.04%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8990 89.90%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.6997 69.97%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.7402 74.02%
Acute Oral Toxicity (c) III 0.5940 59.40%
Estrogen receptor binding + 0.9320 93.20%
Androgen receptor binding + 0.8724 87.24%
Thyroid receptor binding + 0.7423 74.23%
Glucocorticoid receptor binding + 0.8100 81.00%
Aromatase binding + 0.7129 71.29%
PPAR gamma + 0.7930 79.30%
Honey bee toxicity - 0.8684 86.84%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.48% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.26% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.91% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.23% 99.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 92.08% 89.62%
CHEMBL2581 P07339 Cathepsin D 91.74% 98.95%
CHEMBL3194 P02766 Transthyretin 91.51% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 89.49% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.43% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.50% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.84% 97.21%
CHEMBL1255126 O15151 Protein Mdm4 82.93% 90.20%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.46% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.03% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.55% 95.56%
CHEMBL2535 P11166 Glucose transporter 80.16% 98.75%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.04% 95.17%

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.
Broussonetia kazinoki
Broussonetia papyrifera

Cross-Links

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PubChem 21637732
NPASS NPC15543
LOTUS LTS0124131
wikiData Q104946368