Pregeijerene

Details

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Internal ID 68f0cc7a-0e75-420c-9d15-58734a2ada48
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name (1Z,3Z,7Z)-1,7-dimethylcyclodeca-1,3,7-triene
SMILES (Canonical) CC1=CCCC(=CC=CCC1)C
SMILES (Isomeric) C/C/1=C/CC/C(=C\C=C/CC1)/C
InChI InChI=1S/C12H18/c1-11-7-4-3-5-8-12(2)10-6-9-11/h3-4,7,10H,5-6,8-9H2,1-2H3/b4-3-,11-7-,12-10-
InChI Key ACTKFDMFHYIKRY-MBDGBGPPSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C12H18
Molecular Weight 162.27 g/mol
Exact Mass 162.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 4.01
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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(1Z,3Z,7Z)-1,7-dimethylcyclodeca-1,3,7-triene
CHEBI:191546
1,5-dimethylcyclodeca-1,5,7-triene
1,7-Dimethyl-1,3,7-cyclodecatriene

2D Structure

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2D Structure of Pregeijerene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.9789 97.89%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.6417 64.17%
OATP2B1 inhibitior - 0.8594 85.94%
OATP1B1 inhibitior + 0.9749 97.49%
OATP1B3 inhibitior + 0.9594 95.94%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8467 84.67%
P-glycoprotein inhibitior - 0.9889 98.89%
P-glycoprotein substrate - 0.9624 96.24%
CYP3A4 substrate - 0.6663 66.63%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7788 77.88%
CYP3A4 inhibition - 0.9438 94.38%
CYP2C9 inhibition - 0.9178 91.78%
CYP2C19 inhibition - 0.8973 89.73%
CYP2D6 inhibition - 0.9355 93.55%
CYP1A2 inhibition - 0.6809 68.09%
CYP2C8 inhibition - 0.9329 93.29%
CYP inhibitory promiscuity - 0.7420 74.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Warning 0.4778 47.78%
Eye corrosion + 0.7256 72.56%
Eye irritation + 0.9908 99.08%
Skin irritation + 0.7557 75.57%
Skin corrosion - 0.9628 96.28%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3955 39.55%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5798 57.98%
skin sensitisation + 0.9491 94.91%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.7270 72.70%
Acute Oral Toxicity (c) III 0.8254 82.54%
Estrogen receptor binding - 0.9827 98.27%
Androgen receptor binding - 0.7838 78.38%
Thyroid receptor binding - 0.8605 86.05%
Glucocorticoid receptor binding - 0.8702 87.02%
Aromatase binding - 0.8870 88.70%
PPAR gamma - 0.8234 82.34%
Honey bee toxicity - 0.9361 93.61%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9928 99.28%

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 88.70% 95.56%
CHEMBL4208 P20618 Proteasome component C5 82.99% 90.00%

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.
Lallemantia peltata
Pimpinella anisum
Ruta graveolens

Cross-Links

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PubChem 21160126
LOTUS LTS0256071
wikiData Q76511975