1-Acetyl-4-isopropylidene-cyclopentene

Details

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Internal ID 8a9c6fee-e23f-40c4-95c9-0be6d3ce2b51
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name 1-(4-propan-2-ylidenecyclopenten-1-yl)ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O/c1-7(2)9-4-5-10(6-9)8(3)11/h5H,4,6H2,1-3H3
InChI Key CGJITSGJZMOQEU-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.63
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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55873-39-7
DTXSID80286507
1-(4-propan-2-ylidenecyclopenten-1-yl)ethanone
RefChem:227311
DTXCID40237656
NSC46245
SCHEMBL6114233
NSC-46245
1-[4-(Propan-2-ylidene)cyclopent-1-en-1-yl]ethan-1-one

2D Structure

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2D Structure of 1-Acetyl-4-isopropylidene-cyclopentene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.8079 80.79%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.4059 40.59%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.9523 95.23%
OATP1B3 inhibitior + 0.9513 95.13%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8166 81.66%
P-glycoprotein inhibitior - 0.9828 98.28%
P-glycoprotein substrate - 0.9629 96.29%
CYP3A4 substrate - 0.6676 66.76%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate - 0.8550 85.50%
CYP3A4 inhibition - 0.9306 93.06%
CYP2C9 inhibition - 0.8399 83.99%
CYP2C19 inhibition - 0.7907 79.07%
CYP2D6 inhibition - 0.9378 93.78%
CYP1A2 inhibition - 0.7045 70.45%
CYP2C8 inhibition - 0.9839 98.39%
CYP inhibitory promiscuity - 0.6282 62.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6217 62.17%
Carcinogenicity (trinary) Non-required 0.5132 51.32%
Eye corrosion + 0.6327 63.27%
Eye irritation + 0.9818 98.18%
Skin irritation + 0.8384 83.84%
Skin corrosion - 0.8430 84.30%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6404 64.04%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.7439 74.39%
skin sensitisation + 0.9043 90.43%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.4902 49.02%
Acute Oral Toxicity (c) III 0.5432 54.32%
Estrogen receptor binding - 0.9771 97.71%
Androgen receptor binding - 0.7819 78.19%
Thyroid receptor binding - 0.9397 93.97%
Glucocorticoid receptor binding - 0.8842 88.42%
Aromatase binding - 0.8430 84.30%
PPAR gamma - 0.9153 91.53%
Honey bee toxicity - 0.9797 97.97%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9383 93.83%

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 93.51% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.45% 91.11%
CHEMBL4208 P20618 Proteasome component C5 84.64% 90.00%
CHEMBL2581 P07339 Cathepsin D 82.63% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 80.38% 91.19%

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.
Boswellia sacra

Cross-Links

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PubChem 240188
LOTUS LTS0115412
wikiData Q82022262