(1R,2R)-5-ethenyl-3,3-dimethylcyclohex-4-ene-1,2-diol

Details

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Internal ID aa89d95b-b422-4e37-98ec-45691b56a336
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Polyols > 1,2-diols
IUPAC Name (1R,2R)-5-ethenyl-3,3-dimethylcyclohex-4-ene-1,2-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O2/c1-4-7-5-8(11)9(12)10(2,3)6-7/h4,6,8-9,11-12H,1,5H2,2-3H3/t8-,9+/m1/s1
InChI Key LGRVNVACYBVGTJ-BDAKNGLRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O2
Molecular Weight 168.23 g/mol
Exact Mass 168.115029749 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.25
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,2R)-5-ethenyl-3,3-dimethylcyclohex-4-ene-1,2-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9865 98.65%
Caco-2 + 0.7645 76.45%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6828 68.28%
OATP2B1 inhibitior - 0.8612 86.12%
OATP1B1 inhibitior + 0.9158 91.58%
OATP1B3 inhibitior + 0.9625 96.25%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9016 90.16%
P-glycoprotein inhibitior - 0.9791 97.91%
P-glycoprotein substrate - 0.8832 88.32%
CYP3A4 substrate - 0.5795 57.95%
CYP2C9 substrate - 0.8196 81.96%
CYP2D6 substrate - 0.7665 76.65%
CYP3A4 inhibition - 0.8651 86.51%
CYP2C9 inhibition - 0.8547 85.47%
CYP2C19 inhibition - 0.7976 79.76%
CYP2D6 inhibition - 0.9287 92.87%
CYP1A2 inhibition - 0.8931 89.31%
CYP2C8 inhibition - 0.9614 96.14%
CYP inhibitory promiscuity - 0.8764 87.64%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.5856 58.56%
Eye corrosion - 0.9292 92.92%
Eye irritation + 0.7025 70.25%
Skin irritation - 0.5661 56.61%
Skin corrosion - 0.7305 73.05%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6316 63.16%
Micronuclear - 0.6968 69.68%
Hepatotoxicity + 0.6178 61.78%
skin sensitisation + 0.8671 86.71%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.5674 56.74%
Acute Oral Toxicity (c) III 0.8102 81.02%
Estrogen receptor binding - 0.7785 77.85%
Androgen receptor binding - 0.8798 87.98%
Thyroid receptor binding - 0.8347 83.47%
Glucocorticoid receptor binding - 0.7606 76.06%
Aromatase binding - 0.8692 86.92%
PPAR gamma - 0.7045 70.45%
Honey bee toxicity - 0.9116 91.16%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.7657 76.57%

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 97.20% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.09% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.83% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.78% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.78% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.69% 95.89%
CHEMBL1951 P21397 Monoamine oxidase A 82.10% 91.49%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.61% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 21603645
LOTUS LTS0150408
wikiData Q105151556