Acenaphthylene

Details

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Internal ID 9661a739-c38e-4207-89bd-ca0440fdc8cf
Taxonomy Benzenoids > Acenaphthylenes
IUPAC Name acenaphthylene
SMILES (Canonical) C1=CC2=C3C(=C1)C=CC3=CC=C2
SMILES (Isomeric) C1=CC2=C3C(=C1)C=CC3=CC=C2
InChI InChI=1S/C12H8/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-8H
InChI Key HXGDTGSAIMULJN-UHFFFAOYSA-N
Popularity 3,196 references in papers

Physical and Chemical Properties

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Molecular Formula C12H8
Molecular Weight 152.19 g/mol
Exact Mass 152.062600255 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.32
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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208-96-8
Acenaphthalene
Cyclopenta[de]naphthalene
Cyclopenta(de)naphthalene
HSDB 2661
EINECS 205-917-1
NSC 59821
DTXSID3023845
CHEBI:33081
Acenaphthylene, radical ion(1-)
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Acenaphthylene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.9475 94.75%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.7258 72.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9768 97.68%
OATP1B3 inhibitior + 0.9625 96.25%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7321 73.21%
P-glycoprotein inhibitior - 0.9786 97.86%
P-glycoprotein substrate - 0.9797 97.97%
CYP3A4 substrate - 0.7650 76.50%
CYP2C9 substrate - 0.6241 62.41%
CYP2D6 substrate - 0.7140 71.40%
CYP3A4 inhibition - 0.8030 80.30%
CYP2C9 inhibition - 0.7644 76.44%
CYP2C19 inhibition + 0.5205 52.05%
CYP2D6 inhibition - 0.8605 86.05%
CYP1A2 inhibition + 0.7893 78.93%
CYP2C8 inhibition - 0.9421 94.21%
CYP inhibitory promiscuity + 0.7643 76.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Warning 0.4026 40.26%
Eye corrosion + 0.5205 52.05%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8623 86.23%
Skin corrosion - 0.8760 87.60%
Ames mutagenesis + 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7342 73.42%
Micronuclear - 0.6533 65.33%
Hepatotoxicity + 0.8625 86.25%
skin sensitisation + 0.9445 94.45%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.7458 74.58%
Acute Oral Toxicity (c) III 0.8000 80.00%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.6724 67.24%
Thyroid receptor binding - 0.6189 61.89%
Glucocorticoid receptor binding - 0.7233 72.33%
Aromatase binding - 0.6612 66.12%
PPAR gamma - 0.5854 58.54%
Honey bee toxicity - 0.9392 93.92%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.8600 86.00%
Fish aquatic toxicity + 0.9919 99.19%

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 85.29% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.07% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 82.93% 91.49%
CHEMBL3959 P16083 Quinone reductase 2 80.51% 89.49%

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 capillaris
Cornus officinalis
Trichosanthes kirilowii

Cross-Links

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PubChem 9161
NPASS NPC251490
LOTUS LTS0083093
wikiData Q415128