(8R)-8-hydroxy-2-nonyl-5,6,7,8-tetrahydrochromen-4-one

Details

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Internal ID 20db82b2-6c3f-47f9-8541-7d95d4f45746
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name (8R)-8-hydroxy-2-nonyl-5,6,7,8-tetrahydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H28O3/c1-2-3-4-5-6-7-8-10-14-13-17(20)15-11-9-12-16(19)18(15)21-14/h13,16,19H,2-12H2,1H3/t16-/m1/s1
InChI Key UCVKCMREOJPPIO-MRXNPFEDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H28O3
Molecular Weight 292.40 g/mol
Exact Mass 292.20384475 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.30
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8R)-8-hydroxy-2-nonyl-5,6,7,8-tetrahydrochromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.5761 57.61%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.5191 51.91%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.9121 91.21%
OATP1B3 inhibitior + 0.9309 93.09%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5590 55.90%
P-glycoprotein inhibitior - 0.7565 75.65%
P-glycoprotein substrate - 0.7408 74.08%
CYP3A4 substrate + 0.5115 51.15%
CYP2C9 substrate - 0.6200 62.00%
CYP2D6 substrate - 0.7902 79.02%
CYP3A4 inhibition - 0.8126 81.26%
CYP2C9 inhibition - 0.8382 83.82%
CYP2C19 inhibition + 0.6098 60.98%
CYP2D6 inhibition - 0.9059 90.59%
CYP1A2 inhibition + 0.6952 69.52%
CYP2C8 inhibition - 0.7350 73.50%
CYP inhibitory promiscuity - 0.8170 81.70%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6419 64.19%
Eye corrosion - 0.9815 98.15%
Eye irritation - 0.5725 57.25%
Skin irritation - 0.5447 54.47%
Skin corrosion - 0.8532 85.32%
Ames mutagenesis - 0.7315 73.15%
Human Ether-a-go-go-Related Gene inhibition + 0.7733 77.33%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5578 55.78%
skin sensitisation - 0.7653 76.53%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8400 84.00%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.7274 72.74%
Acute Oral Toxicity (c) III 0.5654 56.54%
Estrogen receptor binding + 0.6067 60.67%
Androgen receptor binding + 0.5525 55.25%
Thyroid receptor binding + 0.5883 58.83%
Glucocorticoid receptor binding - 0.5775 57.75%
Aromatase binding - 0.7950 79.50%
PPAR gamma + 0.8492 84.92%
Honey bee toxicity - 0.9791 97.91%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.6569 65.69%
Fish aquatic toxicity + 0.9463 94.63%

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 98.21% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.67% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 90.97% 89.63%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.56% 90.71%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 90.56% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.51% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.36% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.12% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.98% 94.45%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.44% 92.08%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.45% 97.09%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 85.67% 80.33%
CHEMBL240 Q12809 HERG 85.05% 89.76%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 84.78% 90.24%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.25% 92.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.37% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.84% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 82.52% 94.73%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 82.26% 90.24%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.74% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.35% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.15% 93.56%
CHEMBL5255 O00206 Toll-like receptor 4 80.86% 92.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.01% 89.00%

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.
Horsfieldia irya

Cross-Links

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PubChem 162879351
LOTUS LTS0020702
wikiData Q105270168