2,5,9-Trimethylcycloundeca-4,8 dienone

Details

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Internal ID 9dabf276-a7cf-4662-ba82-75dfb2941ada
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name (4Z,8Z)-2,5,9-trimethylcycloundeca-4,8-dien-1-one
SMILES (Canonical) CC1CC=C(CCC=C(CCC1=O)C)C
SMILES (Isomeric) CC1C/C=C(\CC/C=C(\CCC1=O)/C)/C
InChI InChI=1S/C14H22O/c1-11-5-4-6-12(2)8-10-14(15)13(3)9-7-11/h6-7,13H,4-5,8-10H2,1-3H3/b11-7-,12-6-
InChI Key ORGDBIUCLXNWCK-ADUATRDFSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H22O
Molecular Weight 206.32 g/mol
Exact Mass 206.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.80
Atomic LogP (AlogP) 4.05
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,5,9-Trimethylcycloundeca-4,8 dienone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.9484 94.84%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.4618 46.18%
OATP2B1 inhibitior - 0.8451 84.51%
OATP1B1 inhibitior + 0.9658 96.58%
OATP1B3 inhibitior + 0.9384 93.84%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.6428 64.28%
P-glycoprotein inhibitior - 0.9629 96.29%
P-glycoprotein substrate - 0.9366 93.66%
CYP3A4 substrate - 0.5882 58.82%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.7997 79.97%
CYP3A4 inhibition - 0.8980 89.80%
CYP2C9 inhibition - 0.9150 91.50%
CYP2C19 inhibition - 0.8537 85.37%
CYP2D6 inhibition - 0.9463 94.63%
CYP1A2 inhibition - 0.5894 58.94%
CYP2C8 inhibition - 0.9580 95.80%
CYP inhibitory promiscuity - 0.8721 87.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5448 54.48%
Eye corrosion - 0.8151 81.51%
Eye irritation + 0.5842 58.42%
Skin irritation + 0.6761 67.61%
Skin corrosion - 0.9580 95.80%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6431 64.31%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6535 65.35%
skin sensitisation + 0.9270 92.70%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.5787 57.87%
Acute Oral Toxicity (c) III 0.5547 55.47%
Estrogen receptor binding - 0.9643 96.43%
Androgen receptor binding - 0.8033 80.33%
Thyroid receptor binding - 0.8439 84.39%
Glucocorticoid receptor binding - 0.8146 81.46%
Aromatase binding - 0.8290 82.90%
PPAR gamma - 0.8287 82.87%
Honey bee toxicity - 0.9278 92.78%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9556 95.56%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.61% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.70% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.58% 97.25%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.57% 86.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.10% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.09% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.55% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.49% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.74% 96.77%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.28% 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.
Cyperus rotundus

Cross-Links

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PubChem 21160296
LOTUS LTS0225335
wikiData Q105197536