Bornane-2,6-dione

Details

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Internal ID 6e061742-c87f-48c8-bf4c-dcd42c42e086
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 1,7,7-trimethylbicyclo[2.2.1]heptane-2,6-dione
SMILES (Canonical) CC1(C2CC(=O)C1(C(=O)C2)C)C
SMILES (Isomeric) CC1(C2CC(=O)C1(C(=O)C2)C)C
InChI InChI=1S/C10H14O2/c1-9(2)6-4-7(11)10(9,3)8(12)5-6/h6H,4-5H2,1-3H3
InChI Key PCEVUTCFZAQRKV-UHFFFAOYSA-N
Popularity 16 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O2
Molecular Weight 166.22 g/mol
Exact Mass 166.099379685 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.58
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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6-Oxocamphor
2,6-dioxobornane
2,6-diketobornane
NSC670164
1,7,7-Trimethylbicyclo[2.2.1]heptane-2,6-dione
1935-17-7
CHEBI:64893
SCHEMBL5986109
CHEMBL1999760
DTXSID90327612
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Bornane-2,6-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9953 99.53%
Caco-2 + 0.5773 57.73%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.6506 65.06%
OATP2B1 inhibitior - 0.8568 85.68%
OATP1B1 inhibitior + 0.9706 97.06%
OATP1B3 inhibitior + 0.9658 96.58%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9240 92.40%
P-glycoprotein inhibitior - 0.9718 97.18%
P-glycoprotein substrate - 0.9671 96.71%
CYP3A4 substrate - 0.6465 64.65%
CYP2C9 substrate - 0.7800 78.00%
CYP2D6 substrate - 0.8045 80.45%
CYP3A4 inhibition - 0.9539 95.39%
CYP2C9 inhibition - 0.9120 91.20%
CYP2C19 inhibition - 0.8936 89.36%
CYP2D6 inhibition - 0.9616 96.16%
CYP1A2 inhibition - 0.9095 90.95%
CYP2C8 inhibition - 0.9944 99.44%
CYP inhibitory promiscuity - 0.9795 97.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7713 77.13%
Carcinogenicity (trinary) Non-required 0.6057 60.57%
Eye corrosion - 0.8094 80.94%
Eye irritation + 0.9476 94.76%
Skin irritation + 0.6927 69.27%
Skin corrosion - 0.8302 83.02%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7021 70.21%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.7642 76.42%
skin sensitisation + 0.8235 82.35%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.7444 74.44%
Acute Oral Toxicity (c) II 0.6547 65.47%
Estrogen receptor binding - 0.8575 85.75%
Androgen receptor binding - 0.6180 61.80%
Thyroid receptor binding - 0.8239 82.39%
Glucocorticoid receptor binding - 0.8688 86.88%
Aromatase binding - 0.7789 77.89%
PPAR gamma - 0.8049 80.49%
Honey bee toxicity - 0.9096 90.96%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.8006 80.06%

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
CHEMBL1937 Q92769 Histone deacetylase 2 88.31% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.91% 91.11%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.49% 85.30%
CHEMBL2581 P07339 Cathepsin D 85.12% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.44% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.72% 99.23%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 81.10% 85.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.90% 96.09%

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.
Mesua ferrea
Salvia officinalis

Cross-Links

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PubChem 382555
LOTUS LTS0242482
wikiData Q105185545