(Z)-9-Cycloheptadecen-1-one

Details

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Internal ID 1adff287-4478-403c-a169-ed8a85c811e2
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name (9E)-cycloheptadec-9-en-1-one
SMILES (Canonical) C1CCCC=CCCCCCCCC(=O)CCC1
SMILES (Isomeric) C1CCC/C=C/CCCCCCCC(=O)CCC1
InChI InChI=1S/C17H30O/c18-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-17/h1-2H,3-16H2/b2-1+
InChI Key ZKVZSBSZTMPBQR-OWOJBTEDSA-N
Popularity 151 references in papers

Physical and Chemical Properties

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Molecular Formula C17H30O
Molecular Weight 250.40 g/mol
Exact Mass 250.229665576 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 6.10
Atomic LogP (AlogP) 5.59
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Zibeton
9-CYCLOHEPTADECEN-1-ONE
(9Z)-9-Cycloheptadecen-1-one
(9E)-cycloheptadec-9-en-1-one
cis-9-Cycloheptadecen-1-one
trans-Civetone
trans-9-cycloheptadecen-1-one
(Z) - 9 - cycloheptadecen - 1 - one
alpha-trans-Civettone
1502-37-0
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (Z)-9-Cycloheptadecen-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 + 0.8436 84.36%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Mitochondria 0.4821 48.21%
OATP2B1 inhibitior - 0.8526 85.26%
OATP1B1 inhibitior + 0.9654 96.54%
OATP1B3 inhibitior + 0.9635 96.35%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6622 66.22%
P-glycoprotein inhibitior - 0.9129 91.29%
P-glycoprotein substrate - 0.9950 99.50%
CYP3A4 substrate - 0.7761 77.61%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7747 77.47%
CYP3A4 inhibition - 0.9694 96.94%
CYP2C9 inhibition - 0.8779 87.79%
CYP2C19 inhibition - 0.9382 93.82%
CYP2D6 inhibition - 0.9685 96.85%
CYP1A2 inhibition - 0.8439 84.39%
CYP2C8 inhibition - 0.9825 98.25%
CYP inhibitory promiscuity - 0.9199 91.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.6687 66.87%
Eye corrosion + 0.9863 98.63%
Eye irritation + 0.9775 97.75%
Skin irritation + 0.6897 68.97%
Skin corrosion - 0.9640 96.40%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7049 70.49%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.6803 68.03%
skin sensitisation + 0.6916 69.16%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.4582 45.82%
Acute Oral Toxicity (c) II 0.5437 54.37%
Estrogen receptor binding - 0.8197 81.97%
Androgen receptor binding - 0.8974 89.74%
Thyroid receptor binding - 0.7377 73.77%
Glucocorticoid receptor binding - 0.8745 87.45%
Aromatase binding - 0.8435 84.35%
PPAR gamma + 0.6635 66.35%
Honey bee toxicity - 0.9172 91.72%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity - 0.5525 55.25%

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 93.65% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.28% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.65% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 84.06% 89.63%

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.
Eucommia ulmoides

Cross-Links

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PubChem 11334208
NPASS NPC127524