2-(9-Undecenyl)-phenanthrene

Details

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Internal ID e29c775e-4b86-4f83-8ecc-f8c0e4f6c9d9
Taxonomy Benzenoids > Phenanthrenes and derivatives
IUPAC Name 2-undec-9-enylphenanthrene
SMILES (Canonical) CC=CCCCCCCCCC1=CC2=C(C=C1)C3=CC=CC=C3C=C2
SMILES (Isomeric) CC=CCCCCCCCCC1=CC2=C(C=C1)C3=CC=CC=C3C=C2
InChI InChI=1S/C25H30/c1-2-3-4-5-6-7-8-9-10-13-21-16-19-25-23(20-21)18-17-22-14-11-12-15-24(22)25/h2-3,11-12,14-20H,4-10,13H2,1H3
InChI Key KOFSDGBVOUVLSD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C25H30
Molecular Weight 330.50 g/mol
Exact Mass 330.234750957 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 9.60
Atomic LogP (AlogP) 7.84
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-(9-Undecenyl)-phenanthrene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.6250 62.50%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Lysosomes 0.5571 55.71%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.7938 79.38%
OATP1B3 inhibitior + 0.9508 95.08%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9617 96.17%
P-glycoprotein inhibitior + 0.8430 84.30%
P-glycoprotein substrate - 0.7180 71.80%
CYP3A4 substrate + 0.5281 52.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3646 36.46%
CYP3A4 inhibition - 0.9128 91.28%
CYP2C9 inhibition - 0.8591 85.91%
CYP2C19 inhibition - 0.6480 64.80%
CYP2D6 inhibition - 0.9043 90.43%
CYP1A2 inhibition + 0.6367 63.67%
CYP2C8 inhibition + 0.6330 63.30%
CYP inhibitory promiscuity + 0.7051 70.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Danger 0.4033 40.33%
Eye corrosion - 0.6650 66.50%
Eye irritation - 0.6512 65.12%
Skin irritation - 0.5240 52.40%
Skin corrosion - 0.8155 81.55%
Ames mutagenesis + 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9457 94.57%
Micronuclear - 0.9084 90.84%
Hepatotoxicity - 0.6769 67.69%
skin sensitisation + 0.8438 84.38%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.7386 73.86%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.8940 89.40%
Acute Oral Toxicity (c) III 0.7376 73.76%
Estrogen receptor binding + 0.9355 93.55%
Androgen receptor binding + 0.9669 96.69%
Thyroid receptor binding + 0.7130 71.30%
Glucocorticoid receptor binding + 0.6800 68.00%
Aromatase binding + 0.7120 71.20%
PPAR gamma + 0.8328 83.28%
Honey bee toxicity - 0.9039 90.39%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.8700 87.00%
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 96.93% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.73% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.70% 92.08%
CHEMBL2581 P07339 Cathepsin D 95.29% 98.95%
CHEMBL1914 P06276 Butyrylcholinesterase 94.90% 95.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.73% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.47% 95.56%
CHEMBL4296013 Q5VWK5 Interleukin-23 receptor 89.13% 88.00%
CHEMBL3401 O75469 Pregnane X receptor 88.04% 94.73%
CHEMBL2039 P27338 Monoamine oxidase B 87.58% 92.51%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.70% 86.33%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 85.36% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.05% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 84.79% 87.45%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.91% 96.25%
CHEMBL1951 P21397 Monoamine oxidase A 83.09% 91.49%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.91% 95.50%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 82.85% 100.00%
CHEMBL1781 P11387 DNA topoisomerase I 82.47% 97.00%
CHEMBL3902 P09211 Glutathione S-transferase Pi 81.96% 93.81%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.75% 96.00%
CHEMBL1907 P15144 Aminopeptidase N 80.66% 93.31%
CHEMBL2535 P11166 Glucose transporter 80.00% 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.
Kalanchoe pinnata

Cross-Links

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PubChem 163192410
LOTUS LTS0118999
wikiData Q105143788