Acenaphthene

Details

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Internal ID bea4168c-4061-4c4e-a98c-3a3ebb88c570
Taxonomy Benzenoids > Naphthalenes
IUPAC Name 1,2-dihydroacenaphthylene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H10/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-6H,7-8H2
InChI Key CWRYPZZKDGJXCA-UHFFFAOYSA-N
Popularity 4,817 references in papers

Physical and Chemical Properties

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Molecular Formula C12H10
Molecular Weight 154.21 g/mol
Exact Mass 154.078250319 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 2.94
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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83-32-9
1,2-Dihydroacenaphthylene
1,8-Ethylenenaphthalene
peri-Ethylenenaphthalene
Naphthyleneethylene
Acenaphthylene, 1,2-dihydro-
Ethylenenaphthalene
1,8-Dihydroacenaphthalene
DTXSID3021774
V8UT1GAC5Y
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Acenaphthene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.9499 94.99%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.7726 77.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9781 97.81%
OATP1B3 inhibitior + 0.9631 96.31%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7317 73.17%
P-glycoprotein inhibitior - 0.9732 97.32%
P-glycoprotein substrate - 0.9855 98.55%
CYP3A4 substrate - 0.7600 76.00%
CYP2C9 substrate - 0.8117 81.17%
CYP2D6 substrate + 0.4387 43.87%
CYP3A4 inhibition - 0.9025 90.25%
CYP2C9 inhibition - 0.8775 87.75%
CYP2C19 inhibition - 0.7473 74.73%
CYP2D6 inhibition - 0.8845 88.45%
CYP1A2 inhibition + 0.6978 69.78%
CYP2C8 inhibition - 0.9704 97.04%
CYP inhibitory promiscuity + 0.5649 56.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Warning 0.4287 42.87%
Eye corrosion + 0.5636 56.36%
Eye irritation + 0.9950 99.50%
Skin irritation + 0.8623 86.23%
Skin corrosion - 0.8692 86.92%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6241 62.41%
Micronuclear - 0.7514 75.14%
Hepatotoxicity + 0.8194 81.94%
skin sensitisation + 0.8445 84.45%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.5408 54.08%
Acute Oral Toxicity (c) III 0.7135 71.35%
Estrogen receptor binding - 0.4788 47.88%
Androgen receptor binding - 0.8011 80.11%
Thyroid receptor binding - 0.6943 69.43%
Glucocorticoid receptor binding - 0.7539 75.39%
Aromatase binding - 0.6314 63.14%
PPAR gamma - 0.5713 57.13%
Honey bee toxicity - 0.9505 95.05%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.9500 95.00%
Fish aquatic toxicity + 0.9559 95.59%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.74% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 88.46% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.76% 95.56%
CHEMBL3959 P16083 Quinone reductase 2 83.45% 89.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.81% 86.33%
CHEMBL2535 P11166 Glucose transporter 80.05% 98.75%

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.
Artemisia scoparia
Gossypium hirsutum
Salvia coccinea

Cross-Links

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PubChem 6734
NPASS NPC1901
LOTUS LTS0041036
wikiData Q415103