3-Undecylcyclohexa-2,5-diene-1,2,4,5-tetrol

Details

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Internal ID 032511e0-2e8d-444a-9e94-9e56e9882dae
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name 3-undecylcyclohexa-2,5-diene-1,2,4,5-tetrol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H30O4/c1-2-3-4-5-6-7-8-9-10-11-13-16(20)14(18)12-15(19)17(13)21/h12,14,17-21H,2-11H2,1H3
InChI Key DXYGFEDLPPKUBI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H30O4
Molecular Weight 298.40 g/mol
Exact Mass 298.21440943 g/mol
Topological Polar Surface Area (TPSA) 80.90 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Undecylcyclohexa-2,5-diene-1,2,4,5-tetrol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9009 90.09%
Caco-2 - 0.7782 77.82%
Blood Brain Barrier - 0.6879 68.79%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.6916 69.16%
OATP2B1 inhibitior - 0.8514 85.14%
OATP1B1 inhibitior + 0.8773 87.73%
OATP1B3 inhibitior + 0.9555 95.55%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7588 75.88%
BSEP inhibitior - 0.9126 91.26%
P-glycoprotein inhibitior - 0.9108 91.08%
P-glycoprotein substrate - 0.7525 75.25%
CYP3A4 substrate - 0.5441 54.41%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.7519 75.19%
CYP3A4 inhibition - 0.7916 79.16%
CYP2C9 inhibition - 0.8205 82.05%
CYP2C19 inhibition - 0.7965 79.65%
CYP2D6 inhibition - 0.5533 55.33%
CYP1A2 inhibition - 0.8144 81.44%
CYP2C8 inhibition - 0.7000 70.00%
CYP inhibitory promiscuity - 0.6528 65.28%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9023 90.23%
Carcinogenicity (trinary) Non-required 0.6623 66.23%
Eye corrosion - 0.9671 96.71%
Eye irritation - 0.6515 65.15%
Skin irritation - 0.5529 55.29%
Skin corrosion - 0.8986 89.86%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4280 42.80%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5670 56.70%
skin sensitisation + 0.5421 54.21%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.5876 58.76%
Acute Oral Toxicity (c) III 0.6721 67.21%
Estrogen receptor binding + 0.6481 64.81%
Androgen receptor binding - 0.7130 71.30%
Thyroid receptor binding + 0.7040 70.40%
Glucocorticoid receptor binding - 0.4646 46.46%
Aromatase binding - 0.7237 72.37%
PPAR gamma + 0.6526 65.26%
Honey bee toxicity - 0.9391 93.91%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.8326 83.26%
Fish aquatic toxicity + 0.9903 99.03%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.73% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.42% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 93.18% 89.63%
CHEMBL2996 Q05655 Protein kinase C delta 92.42% 97.79%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.22% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.01% 92.86%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.35% 91.11%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.84% 97.29%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 87.28% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.74% 97.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.58% 99.17%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.41% 91.81%
CHEMBL3401 O75469 Pregnane X receptor 80.83% 94.73%

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.
Embelia ribes

Cross-Links

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PubChem 11255005
LOTUS LTS0246697
wikiData Q104991259