3-Cyclopentene-1-acetaldehyde

Details

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Internal ID 87d8e8a2-85e7-4e70-979b-e1ac380de13a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Alpha-hydrogen aldehydes
IUPAC Name 2-cyclopent-3-en-1-ylacetaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H10O/c8-6-5-7-3-1-2-4-7/h1-2,6-7H,3-5H2
InChI Key KMTDBJYJLPMQIB-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H10O
Molecular Weight 110.15 g/mol
Exact Mass 110.073164938 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.54
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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14055-37-9
DTXSID90472979
RefChem:278822
DTXCID80423793
2-(CYCLOPENT-3-EN-1-YL)ACETALDEHYDE
2-cyclopent-3-en-1-ylacetaldehyde
SCHEMBL3355258

2D Structure

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2D Structure of 3-Cyclopentene-1-acetaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.6537 65.37%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Plasma membrane 0.4766 47.66%
OATP2B1 inhibitior - 0.8662 86.62%
OATP1B1 inhibitior + 0.9537 95.37%
OATP1B3 inhibitior + 0.9551 95.51%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9265 92.65%
P-glycoprotein inhibitior - 0.9838 98.38%
P-glycoprotein substrate - 0.9734 97.34%
CYP3A4 substrate - 0.6567 65.67%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.7735 77.35%
CYP3A4 inhibition - 0.9438 94.38%
CYP2C9 inhibition - 0.8948 89.48%
CYP2C19 inhibition - 0.8404 84.04%
CYP2D6 inhibition - 0.9605 96.05%
CYP1A2 inhibition - 0.6186 61.86%
CYP2C8 inhibition - 0.9786 97.86%
CYP inhibitory promiscuity - 0.7409 74.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5317 53.17%
Carcinogenicity (trinary) Non-required 0.5733 57.33%
Eye corrosion + 0.9971 99.71%
Eye irritation + 0.9892 98.92%
Skin irritation + 0.9170 91.70%
Skin corrosion + 0.8418 84.18%
Ames mutagenesis - 0.7254 72.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6979 69.79%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.9063 90.63%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.5393 53.93%
Acute Oral Toxicity (c) III 0.7248 72.48%
Estrogen receptor binding - 0.9178 91.78%
Androgen receptor binding - 0.8984 89.84%
Thyroid receptor binding - 0.8586 85.86%
Glucocorticoid receptor binding - 0.8162 81.62%
Aromatase binding - 0.7396 73.96%
PPAR gamma - 0.8390 83.90%
Honey bee toxicity - 0.7542 75.42%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.6730 67.30%

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 84.49% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.63% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.36% 95.56%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.05% 90.24%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.88% 97.25%

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.
Abrus melanospermus subsp. melanospermus

Cross-Links

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PubChem 11804701
NPASS NPC230102