cis-Carvenone oxide

Details

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Internal ID f1ac6f56-d712-4498-b89f-68811d259db4
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name (1R,3S,6S)-3-methyl-6-propan-2-yl-7-oxabicyclo[4.1.0]heptan-2-one
SMILES (Canonical) CC1CCC2(C(C1=O)O2)C(C)C
SMILES (Isomeric) C[C@H]1CC[C@@]2([C@H](C1=O)O2)C(C)C
InChI InChI=1S/C10H16O2/c1-6(2)10-5-4-7(3)8(11)9(10)12-10/h6-7,9H,4-5H2,1-3H3/t7-,9-,10-/m0/s1
InChI Key ROVXCLHKSQINCN-HGNGGELXSA-N
Popularity 0 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) 29.60 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.78
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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ROVXCLHKSQINCN-HGNGGELXSA-N

2D Structure

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2D Structure of cis-Carvenone oxide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9894 98.94%
Caco-2 + 0.5588 55.88%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5122 51.22%
OATP2B1 inhibitior - 0.8375 83.75%
OATP1B1 inhibitior + 0.9289 92.89%
OATP1B3 inhibitior + 0.9784 97.84%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9348 93.48%
P-glycoprotein inhibitior - 0.9626 96.26%
P-glycoprotein substrate - 0.9314 93.14%
CYP3A4 substrate - 0.5599 55.99%
CYP2C9 substrate - 0.6063 60.63%
CYP2D6 substrate - 0.7560 75.60%
CYP3A4 inhibition - 0.8896 88.96%
CYP2C9 inhibition - 0.8200 82.00%
CYP2C19 inhibition - 0.7307 73.07%
CYP2D6 inhibition - 0.9292 92.92%
CYP1A2 inhibition - 0.5146 51.46%
CYP2C8 inhibition - 0.9820 98.20%
CYP inhibitory promiscuity - 0.9762 97.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5919 59.19%
Eye corrosion - 0.9184 91.84%
Eye irritation + 0.6794 67.94%
Skin irritation + 0.6391 63.91%
Skin corrosion - 0.8190 81.90%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7839 78.39%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.6409 64.09%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.6506 65.06%
Acute Oral Toxicity (c) III 0.5841 58.41%
Estrogen receptor binding - 0.7747 77.47%
Androgen receptor binding - 0.5616 56.16%
Thyroid receptor binding - 0.7791 77.91%
Glucocorticoid receptor binding - 0.8834 88.34%
Aromatase binding - 0.8697 86.97%
PPAR gamma - 0.6970 69.70%
Honey bee toxicity - 0.8751 87.51%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity - 0.5122 51.22%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.47% 97.25%
CHEMBL2581 P07339 Cathepsin D 88.86% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.64% 93.04%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.73% 97.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.33% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.12% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.47% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.80% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.76% 96.77%
CHEMBL4588 P22894 Matrix metalloproteinase 8 81.07% 94.66%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.99% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.51% 95.89%
CHEMBL4072 P07858 Cathepsin B 80.28% 93.67%

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.
Allium victorialis
Blepharis scindica
Ciliosemina pedunculata
Frullania brittoniae
Latua pubiflora
Leionema gracile
Podophyllum hexandrum
Potentilla indica
Rhododendron groenlandicum
Rhododendron tomentosum
Rudbeckia hirta
Schraderanthus viscosa
Solanum stramoniifolium

Cross-Links

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PubChem 6430794
NPASS NPC179574
LOTUS LTS0185223
wikiData Q105242498