3,7-Cyclodecadien-1-one, 10-(1-methylethenyl)-, (E,E)-

Details

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Internal ID 9ba3510e-023d-4442-8012-d45aa39786c4
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name (3E,7E)-10-prop-1-en-2-ylcyclodeca-3,7-dien-1-one
SMILES (Canonical) CC(=C)C1CC=CCCC=CCC1=O
SMILES (Isomeric) CC(=C)C1C/C=C/CC/C=C/CC1=O
InChI InChI=1S/C13H18O/c1-11(2)12-9-7-5-3-4-6-8-10-13(12)14/h5-8,12H,1,3-4,9-10H2,2H3/b7-5+,8-6+
InChI Key VJWZVZISFZTZGU-KQQUZDAGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H18O
Molecular Weight 190.28 g/mol
Exact Mass 190.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.43
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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VJWZVZISFZTZGU-KQQUZDAGSA-N
10-Isopropenyl-3,7-cyclodecadien-1-one #

2D Structure

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2D Structure of 3,7-Cyclodecadien-1-one, 10-(1-methylethenyl)-, (E,E)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 - 0.5568 55.68%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.5284 52.84%
OATP2B1 inhibitior - 0.8582 85.82%
OATP1B1 inhibitior + 0.9642 96.42%
OATP1B3 inhibitior + 0.8985 89.85%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8319 83.19%
P-glycoprotein inhibitior - 0.9899 98.99%
P-glycoprotein substrate - 0.9382 93.82%
CYP3A4 substrate - 0.5681 56.81%
CYP2C9 substrate - 0.8176 81.76%
CYP2D6 substrate - 0.8065 80.65%
CYP3A4 inhibition - 0.9399 93.99%
CYP2C9 inhibition - 0.9224 92.24%
CYP2C19 inhibition - 0.8204 82.04%
CYP2D6 inhibition - 0.9387 93.87%
CYP1A2 inhibition - 0.6199 61.99%
CYP2C8 inhibition - 0.9597 95.97%
CYP inhibitory promiscuity - 0.8349 83.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.5915 59.15%
Eye corrosion - 0.5952 59.52%
Eye irritation + 0.8867 88.67%
Skin irritation + 0.5433 54.33%
Skin corrosion - 0.9388 93.88%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5511 55.11%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.7086 70.86%
skin sensitisation + 0.8824 88.24%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.6368 63.68%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6061 60.61%
Acute Oral Toxicity (c) III 0.7649 76.49%
Estrogen receptor binding - 0.9491 94.91%
Androgen receptor binding - 0.6827 68.27%
Thyroid receptor binding - 0.8473 84.73%
Glucocorticoid receptor binding - 0.7005 70.05%
Aromatase binding - 0.8679 86.79%
PPAR gamma - 0.7311 73.11%
Honey bee toxicity - 0.8846 88.46%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9501 95.01%

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 94.73% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.58% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.66% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.43% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.78% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.53% 85.14%

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.
Curcuma kwangsiensis
Curcuma phaeocaulis
Curcuma wenyujin
Curcuma zedoaria

Cross-Links

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PubChem 5369944
NPASS NPC71995