2,7-dihydroxy-9-methyl-3,6-di(undecyl)-9H-xanthene-1,4,5,8-tetrone

Details

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Internal ID 34599b38-28e0-4bc9-81da-58d60236372d
Taxonomy Organoheterocyclic compounds > Pyrans
IUPAC Name 2,7-dihydroxy-9-methyl-3,6-di(undecyl)-9H-xanthene-1,4,5,8-tetrone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C36H52O7/c1-4-6-8-10-12-14-16-18-20-22-25-29(37)33(41)27-24(3)28-34(42)30(38)26(32(40)36(28)43-35(27)31(25)39)23-21-19-17-15-13-11-9-7-5-2/h24,37-38H,4-23H2,1-3H3
InChI Key PSIOYNVYDPZURD-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C36H52O7
Molecular Weight 596.80 g/mol
Exact Mass 596.37130399 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP 11.50
Atomic LogP (AlogP) 8.93
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 20

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,7-dihydroxy-9-methyl-3,6-di(undecyl)-9H-xanthene-1,4,5,8-tetrone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9739 97.39%
Caco-2 - 0.7507 75.07%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6853 68.53%
OATP2B1 inhibitior - 0.5697 56.97%
OATP1B1 inhibitior + 0.9013 90.13%
OATP1B3 inhibitior + 0.9294 92.94%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.7564 75.64%
BSEP inhibitior - 0.5233 52.33%
P-glycoprotein inhibitior + 0.5862 58.62%
P-glycoprotein substrate - 0.8383 83.83%
CYP3A4 substrate - 0.5110 51.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8681 86.81%
CYP3A4 inhibition + 0.5769 57.69%
CYP2C9 inhibition - 0.8010 80.10%
CYP2C19 inhibition - 0.7499 74.99%
CYP2D6 inhibition - 0.8227 82.27%
CYP1A2 inhibition - 0.6716 67.16%
CYP2C8 inhibition - 0.8556 85.56%
CYP inhibitory promiscuity - 0.7435 74.35%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6569 65.69%
Eye corrosion - 0.9873 98.73%
Eye irritation - 0.6551 65.51%
Skin irritation - 0.5288 52.88%
Skin corrosion - 0.9304 93.04%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5653 56.53%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.5331 53.31%
skin sensitisation - 0.7926 79.26%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.7319 73.19%
Acute Oral Toxicity (c) III 0.4644 46.44%
Estrogen receptor binding + 0.6448 64.48%
Androgen receptor binding + 0.6770 67.70%
Thyroid receptor binding - 0.5680 56.80%
Glucocorticoid receptor binding - 0.5254 52.54%
Aromatase binding - 0.5600 56.00%
PPAR gamma + 0.5554 55.54%
Honey bee toxicity - 0.9697 96.97%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.7682 76.82%
Fish aquatic toxicity + 0.9936 99.36%

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
CHEMBL2581 P07339 Cathepsin D 96.76% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.33% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.62% 97.25%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.07% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 90.14% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.94% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.06% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.31% 95.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.18% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.53% 99.17%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 80.11% 96.37%

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.
Myrsine africana

Cross-Links

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PubChem 101762593
NPASS NPC93334
LOTUS LTS0141444
wikiData Q105214198