Biphenanthrene

Details

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Internal ID f9d69f97-80bf-44c8-96c9-12efa92c52dd
Taxonomy Benzenoids > Phenanthrenes and derivatives
IUPAC Name 1-phenanthren-1-ylphenanthrene
SMILES (Canonical) C1=CC=C2C(=C1)C=CC3=C2C=CC=C3C4=CC=CC5=C4C=CC6=CC=CC=C65
SMILES (Isomeric) C1=CC=C2C(=C1)C=CC3=C2C=CC=C3C4=CC=CC5=C4C=CC6=CC=CC=C65
InChI InChI=1S/C28H18/c1-3-9-21-19(7-1)15-17-27-23(21)11-5-13-25(27)26-14-6-12-24-22-10-4-2-8-20(22)16-18-28(24)26/h1-18H
InChI Key VQECOUFHPVSSCD-UHFFFAOYSA-N
Popularity 33 references in papers

Physical and Chemical Properties

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Molecular Formula C28H18
Molecular Weight 354.40 g/mol
Exact Mass 354.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 8.50
Atomic LogP (AlogP) 7.97
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1-phenanthren-1-ylphenanthrene

2D Structure

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2D Structure of Biphenanthrene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.5586 55.86%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.6636 66.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9588 95.88%
OATP1B3 inhibitior + 0.9614 96.14%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.9200 92.00%
P-glycoprotein inhibitior - 0.7350 73.50%
P-glycoprotein substrate - 0.9515 95.15%
CYP3A4 substrate - 0.6578 65.78%
CYP2C9 substrate - 0.8170 81.70%
CYP2D6 substrate + 0.3939 39.39%
CYP3A4 inhibition - 0.9183 91.83%
CYP2C9 inhibition - 0.8551 85.51%
CYP2C19 inhibition - 0.8271 82.71%
CYP2D6 inhibition - 0.9437 94.37%
CYP1A2 inhibition + 0.6163 61.63%
CYP2C8 inhibition - 0.8137 81.37%
CYP inhibitory promiscuity + 0.6193 61.93%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Warning 0.4549 45.49%
Eye corrosion - 0.6144 61.44%
Eye irritation + 0.9887 98.87%
Skin irritation + 0.8188 81.88%
Skin corrosion - 0.8667 86.67%
Ames mutagenesis + 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6907 69.07%
Micronuclear - 0.6376 63.76%
Hepatotoxicity + 0.8323 83.23%
skin sensitisation + 0.8595 85.95%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5887 58.87%
Acute Oral Toxicity (c) III 0.7630 76.30%
Estrogen receptor binding + 0.9742 97.42%
Androgen receptor binding + 0.9400 94.00%
Thyroid receptor binding + 0.7722 77.22%
Glucocorticoid receptor binding + 0.8492 84.92%
Aromatase binding + 0.8510 85.10%
PPAR gamma + 0.8789 87.89%
Honey bee toxicity - 0.9229 92.29%
Biodegradation - 1.0000 100.00%
Crustacea aquatic toxicity + 0.9700 97.00%
Fish aquatic toxicity + 0.9820 98.20%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.76% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.36% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 86.67% 91.49%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 84.96% 96.67%
CHEMBL2581 P07339 Cathepsin D 82.99% 98.95%
CHEMBL2535 P11166 Glucose transporter 82.57% 98.75%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 82.18% 94.67%

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.
Bletilla striata

Cross-Links

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PubChem 21709721
LOTUS LTS0011276
wikiData Q105291196