5-Ethylidene-1-methylcycloheptene

Details

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Internal ID 705d9779-ed43-4a2a-b613-7c08966e90dc
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 5-ethylidene-1-methylcycloheptene
SMILES (Canonical) CC=C1CCC=C(CC1)C
SMILES (Isomeric) CC=C1CCC=C(CC1)C
InChI InChI=1S/C10H16/c1-3-10-6-4-5-9(2)7-8-10/h3,5H,4,6-8H2,1-2H3
InChI Key HQVYRYNHRRUKSO-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H16
Molecular Weight 136.23 g/mol
Exact Mass 136.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.45
H-Bond Acceptor 0
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 5-Ethylidene-1-methylcycloheptene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9892 98.92%
Caco-2 + 0.9323 93.23%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.6337 63.37%
OATP2B1 inhibitior - 0.8474 84.74%
OATP1B1 inhibitior + 0.9574 95.74%
OATP1B3 inhibitior + 0.9439 94.39%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8895 88.95%
P-glycoprotein inhibitior - 0.9844 98.44%
P-glycoprotein substrate - 0.9619 96.19%
CYP3A4 substrate - 0.6815 68.15%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.7601 76.01%
CYP3A4 inhibition - 0.9712 97.12%
CYP2C9 inhibition - 0.9303 93.03%
CYP2C19 inhibition - 0.9251 92.51%
CYP2D6 inhibition - 0.9335 93.35%
CYP1A2 inhibition - 0.7377 73.77%
CYP2C8 inhibition - 0.9538 95.38%
CYP inhibitory promiscuity - 0.8178 81.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Warning 0.4507 45.07%
Eye corrosion + 0.7670 76.70%
Eye irritation + 0.9437 94.37%
Skin irritation + 0.8093 80.93%
Skin corrosion - 0.9721 97.21%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5526 55.26%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.9238 92.38%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.5556 55.56%
Acute Oral Toxicity (c) III 0.8849 88.49%
Estrogen receptor binding - 0.9826 98.26%
Androgen receptor binding - 0.8663 86.63%
Thyroid receptor binding - 0.9267 92.67%
Glucocorticoid receptor binding - 0.9038 90.38%
Aromatase binding - 0.8931 89.31%
PPAR gamma - 0.8782 87.82%
Honey bee toxicity - 0.9197 91.97%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9929 99.29%

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 89.22% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 83.63% 94.73%

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.
Chrysanthemum indicum

Cross-Links

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PubChem 27253
LOTUS LTS0119180
wikiData Q105032459