hydron;7-oxo-5-propan-2-ylcyclohepta-1,3,5-trien-1-olate

Details

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Internal ID 3f3f4c37-5f58-44f5-8c04-00a798fe1d2d
Taxonomy Hydrocarbon derivatives > Tropones > Tropolones
IUPAC Name hydron;7-oxo-5-propan-2-ylcyclohepta-1,3,5-trien-1-olate
SMILES (Canonical) [H+].CC(C)C1=CC(=O)C(=CC=C1)[O-]
SMILES (Isomeric) [H+].CC(C)C1=CC(=O)C(=CC=C1)[O-]
InChI InChI=1S/C10H12O2/c1-7(2)8-4-3-5-9(11)10(12)6-8/h3-7H,1-2H3,(H,11,12)
InChI Key FUWUEFKEXZQKKA-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O2
Molecular Weight 164.20 g/mol
Exact Mass 164.083729621 g/mol
Topological Polar Surface Area (TPSA) 40.10 Ų
XlogP 0.00
Atomic LogP (AlogP) 1.36
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of hydron;7-oxo-5-propan-2-ylcyclohepta-1,3,5-trien-1-olate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 + 0.8476 84.76%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.8403 84.03%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9575 95.75%
OATP1B3 inhibitior + 0.9631 96.31%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9412 94.12%
P-glycoprotein inhibitior - 0.9689 96.89%
P-glycoprotein substrate - 0.9249 92.49%
CYP3A4 substrate - 0.6790 67.90%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.8548 85.48%
CYP3A4 inhibition - 0.9381 93.81%
CYP2C9 inhibition - 0.8630 86.30%
CYP2C19 inhibition - 0.7430 74.30%
CYP2D6 inhibition - 0.9091 90.91%
CYP1A2 inhibition + 0.6453 64.53%
CYP2C8 inhibition - 0.9872 98.72%
CYP inhibitory promiscuity - 0.8633 86.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.6304 63.04%
Eye corrosion + 0.8018 80.18%
Eye irritation + 0.9884 98.84%
Skin irritation + 0.6407 64.07%
Skin corrosion + 0.7128 71.28%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8560 85.60%
Micronuclear - 0.6226 62.26%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.6414 64.14%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.4505 45.05%
Acute Oral Toxicity (c) III 0.8449 84.49%
Estrogen receptor binding - 0.8188 81.88%
Androgen receptor binding - 0.6054 60.54%
Thyroid receptor binding - 0.6552 65.52%
Glucocorticoid receptor binding - 0.8787 87.87%
Aromatase binding - 0.7847 78.47%
PPAR gamma - 0.8322 83.22%
Honey bee toxicity - 0.8914 89.14%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.8651 86.51%

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
CHEMBL2581 P07339 Cathepsin D 97.09% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.69% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 89.08% 93.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.97% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 87.22% 94.73%
CHEMBL2535 P11166 Glucose transporter 86.86% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.66% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.41% 91.11%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.95% 94.80%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.79% 93.40%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.75% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.29% 94.45%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.21% 100.00%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 82.05% 97.23%
CHEMBL1907588 P02708 Acetylcholine receptor; alpha1/beta1/delta/gamma 81.53% 98.33%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.30% 93.56%

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 71773484
NPASS NPC46565
ChEMBL CHEMBL48310