kosamol R

Details

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Internal ID fd9cb6a3-d654-460e-b2e8-610ff6c5f7df
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 8-prenylated flavans > 8-prenylated flavanones
IUPAC Name 7-hydroxy-2-(2-hydroxyphenyl)-5-methoxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H30O5/c1-15(2)10-11-17(16(3)4)12-19-21(28)13-24(30-5)25-22(29)14-23(31-26(19)25)18-8-6-7-9-20(18)27/h6-10,13,17,23,27-28H,3,11-12,14H2,1-2,4-5H3
InChI Key NREGVTHCHKOXLC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H30O5
Molecular Weight 422.50 g/mol
Exact Mass 422.20932405 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 5.90
Atomic LogP (AlogP) 5.90
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of kosamol R

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9880 98.80%
Caco-2 + 0.5234 52.34%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7997 79.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8428 84.28%
OATP1B3 inhibitior + 0.9045 90.45%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9265 92.65%
P-glycoprotein inhibitior + 0.7667 76.67%
P-glycoprotein substrate - 0.6105 61.05%
CYP3A4 substrate + 0.6482 64.82%
CYP2C9 substrate - 0.7880 78.80%
CYP2D6 substrate - 0.7350 73.50%
CYP3A4 inhibition - 0.7286 72.86%
CYP2C9 inhibition + 0.8193 81.93%
CYP2C19 inhibition + 0.9223 92.23%
CYP2D6 inhibition - 0.5613 56.13%
CYP1A2 inhibition + 0.8118 81.18%
CYP2C8 inhibition + 0.6224 62.24%
CYP inhibitory promiscuity + 0.8899 88.99%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.7143 71.43%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.8210 82.10%
Skin irritation - 0.7884 78.84%
Skin corrosion - 0.9443 94.43%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7901 79.01%
Micronuclear - 0.5141 51.41%
Hepatotoxicity + 0.7302 73.02%
skin sensitisation - 0.8234 82.34%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5472 54.72%
Estrogen receptor binding + 0.8352 83.52%
Androgen receptor binding + 0.6325 63.25%
Thyroid receptor binding + 0.6464 64.64%
Glucocorticoid receptor binding + 0.8370 83.70%
Aromatase binding - 0.5510 55.10%
PPAR gamma + 0.7860 78.60%
Honey bee toxicity - 0.6901 69.01%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9930 99.30%

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 99.33% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.60% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.84% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.08% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.03% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.75% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.58% 99.17%
CHEMBL240 Q12809 HERG 89.18% 89.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.93% 86.33%
CHEMBL2535 P11166 Glucose transporter 88.16% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.56% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 84.89% 94.73%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.35% 91.07%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.31% 89.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.98% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.09% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.00% 97.14%

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.
Sophora flavescens

Cross-Links

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PubChem 74819350
LOTUS LTS0000823
wikiData Q105184458