Cyclohexene, 1-propyl-

Details

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Internal ID 155c2396-7cd1-4af3-a01d-d7113901139c
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1-propylcyclohexene
SMILES (Canonical) CCCC1=CCCCC1
SMILES (Isomeric) CCCC1=CCCCC1
InChI InChI=1S/C9H16/c1-2-6-9-7-4-3-5-8-9/h7H,2-6,8H2,1H3
InChI Key WCPWJMLXSZIWOP-UHFFFAOYSA-N
Popularity 31 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16
Molecular Weight 124.22 g/mol
Exact Mass 124.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.29
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Cyclohexene,1-propyl-
2539-75-5
1-propylcyclohexene
1-Propyl-1-cyclohexene
propylcyclohexene
1-Propylcyclohexene-1
1-Propyl-1-cyclohexene #
DTXSID80180036
WCPWJMLXSZIWOP-UHFFFAOYSA-N

2D Structure

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2D Structure of Cyclohexene, 1-propyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.9778 97.78%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Plasma membrane 0.3680 36.80%
OATP2B1 inhibitior - 0.8384 83.84%
OATP1B1 inhibitior + 0.9291 92.91%
OATP1B3 inhibitior + 0.9331 93.31%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9371 93.71%
P-glycoprotein inhibitior - 0.9876 98.76%
P-glycoprotein substrate - 0.9392 93.92%
CYP3A4 substrate - 0.7288 72.88%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9338 93.38%
CYP2C9 inhibition - 0.9230 92.30%
CYP2C19 inhibition - 0.9220 92.20%
CYP2D6 inhibition - 0.9243 92.43%
CYP1A2 inhibition - 0.6269 62.69%
CYP2C8 inhibition - 0.8753 87.53%
CYP inhibitory promiscuity + 0.6432 64.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Warning 0.5515 55.15%
Eye corrosion + 0.8791 87.91%
Eye irritation + 0.9878 98.78%
Skin irritation + 0.6753 67.53%
Skin corrosion - 0.9834 98.34%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5088 50.88%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.9678 96.78%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.7821 78.21%
Acute Oral Toxicity (c) III 0.9346 93.46%
Estrogen receptor binding - 0.9793 97.93%
Androgen receptor binding - 0.8914 89.14%
Thyroid receptor binding - 0.9092 90.92%
Glucocorticoid receptor binding - 0.9097 90.97%
Aromatase binding - 0.8521 85.21%
PPAR gamma - 0.8900 89.00%
Honey bee toxicity - 0.9681 96.81%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9933 99.33%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.34% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.17% 97.25%
CHEMBL2581 P07339 Cathepsin D 92.14% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 88.37% 89.63%
CHEMBL4208 P20618 Proteasome component C5 88.05% 90.00%
CHEMBL221 P23219 Cyclooxygenase-1 81.86% 90.17%

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.
Caryocar coriaceum

Cross-Links

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PubChem 107833
LOTUS LTS0009520
wikiData Q81985484