(-)-2,6,6-Trimethyl-2(R)-vinyltetrahydropyran-5-one

Details

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Internal ID 5abbd510-d457-4f3f-8ec0-bfd82377b99f
Taxonomy Organoheterocyclic compounds > Oxanes
IUPAC Name (6R)-6-ethenyl-2,2,6-trimethyloxan-3-one
SMILES (Canonical) CC1(C(=O)CCC(O1)(C)C=C)C
SMILES (Isomeric) C[C@@]1(CCC(=O)C(O1)(C)C)C=C
InChI InChI=1S/C10H16O2/c1-5-10(4)7-6-8(11)9(2,3)12-10/h5H,1,6-7H2,2-4H3/t10-/m0/s1
InChI Key ATQPZCOAQSYTPR-JTQLQIEISA-N
Popularity 1 reference 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) 26.30 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.09
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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(-)-2,6,6-TRIMETHYL-2(R)-VINYLTETRAHYDROPYRAN-5-ONE
[2R,(?)]-2,6,6-Trimethyl-2beta-vinyl-3,4,5,6-tetrahydro-2H-pyran-5-one

2D Structure

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2D Structure of (-)-2,6,6-Trimethyl-2(R)-vinyltetrahydropyran-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 + 0.8006 80.06%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.6416 64.16%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.9420 94.20%
OATP1B3 inhibitior + 0.9486 94.86%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9360 93.60%
P-glycoprotein inhibitior - 0.9797 97.97%
P-glycoprotein substrate - 0.9884 98.84%
CYP3A4 substrate - 0.5358 53.58%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.7887 78.87%
CYP3A4 inhibition - 0.7077 70.77%
CYP2C9 inhibition - 0.9061 90.61%
CYP2C19 inhibition - 0.7511 75.11%
CYP2D6 inhibition - 0.9096 90.96%
CYP1A2 inhibition - 0.5677 56.77%
CYP2C8 inhibition - 0.9403 94.03%
CYP inhibitory promiscuity - 0.9444 94.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8228 82.28%
Carcinogenicity (trinary) Non-required 0.5707 57.07%
Eye corrosion - 0.8796 87.96%
Eye irritation + 0.7571 75.71%
Skin irritation + 0.6751 67.51%
Skin corrosion - 0.8199 81.99%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7315 73.15%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.6251 62.51%
skin sensitisation + 0.8090 80.90%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.7655 76.55%
Acute Oral Toxicity (c) III 0.8382 83.82%
Estrogen receptor binding - 0.8677 86.77%
Androgen receptor binding - 0.8125 81.25%
Thyroid receptor binding - 0.8721 87.21%
Glucocorticoid receptor binding - 0.8156 81.56%
Aromatase binding - 0.8286 82.86%
PPAR gamma - 0.8161 81.61%
Honey bee toxicity - 0.9116 91.16%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.7096 70.96%

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 92.91% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.45% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 85.83% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.36% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.22% 93.04%
CHEMBL2581 P07339 Cathepsin D 80.81% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.38% 100.00%

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.
Artemisia scoparia
Ficus carica
Tanacetum vulgare

Cross-Links

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PubChem 101607907
NPASS NPC240492
LOTUS LTS0171025
wikiData Q63391926