10-(4-Hydroxyphenyl)-3,5,6-trimethyl-3-(4,8,12-trimethyltridecyl)-1,2,9,10-tetrahydropyrano[3,2-f]chromen-8-one

Details

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Internal ID 55964904-8ece-4b7a-8878-b2bda976a259
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name 10-(4-hydroxyphenyl)-3,5,6-trimethyl-3-(4,8,12-trimethyltridecyl)-1,2,9,10-tetrahydropyrano[3,2-f]chromen-8-one
SMILES (Canonical) CC1=C(C2=C(C(CC(=O)O2)C3=CC=C(C=C3)O)C4=C1OC(CC4)(C)CCCC(C)CCCC(C)CCCC(C)C)C
SMILES (Isomeric) CC1=C(C2=C(C(CC(=O)O2)C3=CC=C(C=C3)O)C4=C1OC(CC4)(C)CCCC(C)CCCC(C)CCCC(C)C)C
InChI InChI=1S/C37H54O4/c1-24(2)11-8-12-25(3)13-9-14-26(4)15-10-21-37(7)22-20-31-34-32(29-16-18-30(38)19-17-29)23-33(39)40-36(34)28(6)27(5)35(31)41-37/h16-19,24-26,32,38H,8-15,20-23H2,1-7H3
InChI Key OIWXAKXWTNBOBE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C37H54O4
Molecular Weight 562.80 g/mol
Exact Mass 562.40221020 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 11.50
Atomic LogP (AlogP) 9.97
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10-(4-Hydroxyphenyl)-3,5,6-trimethyl-3-(4,8,12-trimethyltridecyl)-1,2,9,10-tetrahydropyrano[3,2-f]chromen-8-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9825 98.25%
Caco-2 - 0.7081 70.81%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.8405 84.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8691 86.91%
OATP1B3 inhibitior + 0.9064 90.64%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9838 98.38%
P-glycoprotein inhibitior + 0.7649 76.49%
P-glycoprotein substrate + 0.5275 52.75%
CYP3A4 substrate + 0.6881 68.81%
CYP2C9 substrate - 0.5914 59.14%
CYP2D6 substrate - 0.7327 73.27%
CYP3A4 inhibition - 0.7392 73.92%
CYP2C9 inhibition - 0.8516 85.16%
CYP2C19 inhibition - 0.9240 92.40%
CYP2D6 inhibition - 0.9471 94.71%
CYP1A2 inhibition - 0.8771 87.71%
CYP2C8 inhibition + 0.6948 69.48%
CYP inhibitory promiscuity - 0.9180 91.80%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7442 74.42%
Eye corrosion - 0.9936 99.36%
Eye irritation - 0.9223 92.23%
Skin irritation - 0.7752 77.52%
Skin corrosion - 0.9575 95.75%
Ames mutagenesis - 0.7837 78.37%
Human Ether-a-go-go-Related Gene inhibition + 0.8179 81.79%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.7425 74.25%
skin sensitisation - 0.9045 90.45%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.8890 88.90%
Acute Oral Toxicity (c) III 0.5207 52.07%
Estrogen receptor binding + 0.8534 85.34%
Androgen receptor binding + 0.8254 82.54%
Thyroid receptor binding + 0.5192 51.92%
Glucocorticoid receptor binding + 0.7536 75.36%
Aromatase binding + 0.6727 67.27%
PPAR gamma + 0.5254 52.54%
Honey bee toxicity - 0.8629 86.29%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9962 99.62%

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 99.05% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.53% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.58% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.03% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.81% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 93.02% 90.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.84% 96.09%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 89.97% 85.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.84% 89.00%
CHEMBL242 Q92731 Estrogen receptor beta 88.98% 98.35%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.72% 93.56%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 87.53% 85.00%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 87.15% 90.93%
CHEMBL1907 P15144 Aminopeptidase N 86.48% 93.31%
CHEMBL1951 P21397 Monoamine oxidase A 86.23% 91.49%
CHEMBL3902 P09211 Glutathione S-transferase Pi 85.89% 93.81%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.29% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.10% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.39% 86.33%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.47% 100.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.40% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 80.05% 97.79%

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.
Prunus grayana

Cross-Links

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PubChem 14580537
LOTUS LTS0132341
wikiData Q105192902