2-Dec-9-enylphenanthrene

Details

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Internal ID 419bf212-eedc-4a55-bfd1-23a887dd6232
Taxonomy Benzenoids > Phenanthrenes and derivatives
IUPAC Name 2-dec-9-enylphenanthrene
SMILES (Canonical) C=CCCCCCCCCC1=CC2=C(C=C1)C3=CC=CC=C3C=C2
SMILES (Isomeric) C=CCCCCCCCCC1=CC2=C(C=C1)C3=CC=CC=C3C=C2
InChI InChI=1S/C24H28/c1-2-3-4-5-6-7-8-9-12-20-15-18-24-22(19-20)17-16-21-13-10-11-14-23(21)24/h2,10-11,13-19H,1,3-9,12H2
InChI Key QCSSPUSNCHKEOS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H28
Molecular Weight 316.50 g/mol
Exact Mass 316.219100893 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 9.40
Atomic LogP (AlogP) 7.45
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Dec-9-enylphenanthrene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 - 0.5448 54.48%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Plasma membrane 0.5422 54.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8965 89.65%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.8876 88.76%
P-glycoprotein inhibitior + 0.7420 74.20%
P-glycoprotein substrate - 0.8188 81.88%
CYP3A4 substrate + 0.5063 50.63%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate + 0.4550 45.50%
CYP3A4 inhibition - 0.8456 84.56%
CYP2C9 inhibition - 0.7508 75.08%
CYP2C19 inhibition - 0.5111 51.11%
CYP2D6 inhibition - 0.8793 87.93%
CYP1A2 inhibition + 0.6436 64.36%
CYP2C8 inhibition + 0.7424 74.24%
CYP inhibitory promiscuity + 0.7846 78.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.4274 42.74%
Eye corrosion + 0.5000 50.00%
Eye irritation + 0.7029 70.29%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.7482 74.82%
Ames mutagenesis + 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9061 90.61%
Micronuclear - 0.8678 86.78%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation + 0.8057 80.57%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.8215 82.15%
Acute Oral Toxicity (c) III 0.8648 86.48%
Estrogen receptor binding + 0.9678 96.78%
Androgen receptor binding + 0.9635 96.35%
Thyroid receptor binding + 0.7269 72.69%
Glucocorticoid receptor binding + 0.7793 77.93%
Aromatase binding + 0.8821 88.21%
PPAR gamma + 0.8498 84.98%
Honey bee toxicity - 0.7734 77.34%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.8300 83.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL240 Q12809 HERG 99.20% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.44% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.81% 92.08%
CHEMBL2581 P07339 Cathepsin D 91.78% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 91.73% 91.49%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 90.81% 85.94%
CHEMBL1914 P06276 Butyrylcholinesterase 90.79% 95.00%
CHEMBL2039 P27338 Monoamine oxidase B 88.43% 92.51%
CHEMBL3902 P09211 Glutathione S-transferase Pi 87.82% 93.81%
CHEMBL2885 P07451 Carbonic anhydrase III 87.70% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.67% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.41% 95.56%
CHEMBL4296013 Q5VWK5 Interleukin-23 receptor 86.98% 88.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.65% 86.33%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 84.76% 83.57%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.80% 96.25%
CHEMBL3401 O75469 Pregnane X receptor 83.35% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.28% 95.50%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.94% 93.99%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 82.24% 85.49%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.22% 91.71%
CHEMBL3959 P16083 Quinone reductase 2 81.15% 89.49%
CHEMBL3891 P07384 Calpain 1 81.13% 93.04%

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.
Kalanchoe pinnata

Cross-Links

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PubChem 129682058
LOTUS LTS0141256
wikiData Q105218554