Phenanthren-2-ol

Details

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Internal ID bc631d54-b464-48bc-9d9f-909c9cacb4b4
Taxonomy Benzenoids > Phenanthrenes and derivatives > Phenanthrols
IUPAC Name phenanthren-2-ol
SMILES (Canonical) C1=CC=C2C(=C1)C=CC3=C2C=CC(=C3)O
SMILES (Isomeric) C1=CC=C2C(=C1)C=CC3=C2C=CC(=C3)O
InChI InChI=1S/C14H10O/c15-12-7-8-14-11(9-12)6-5-10-3-1-2-4-13(10)14/h1-9,15H
InChI Key YPWLZGITFNGGKW-UHFFFAOYSA-N
Popularity 103 references in papers

Physical and Chemical Properties

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Molecular Formula C14H10O
Molecular Weight 194.23 g/mol
Exact Mass 194.073164938 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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605-55-0
2-Phenanthrenol
2-Phenanthrol
2-hydroxyphenanthrene
2-Hydroxy-phenanthrene
PHENANTHRENOL
JZU8H3H6VM
NSC-2576
2-Hydroxyphenanthrene 10 microg/mL in Acetonitrile
NSC 2576
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Phenanthren-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8013 80.13%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.4551 45.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8857 88.57%
OATP1B3 inhibitior + 0.9539 95.39%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6447 64.47%
P-glycoprotein inhibitior - 0.9650 96.50%
P-glycoprotein substrate - 0.9605 96.05%
CYP3A4 substrate - 0.6605 66.05%
CYP2C9 substrate - 0.8333 83.33%
CYP2D6 substrate + 0.3949 39.49%
CYP3A4 inhibition - 0.9377 93.77%
CYP2C9 inhibition - 0.8050 80.50%
CYP2C19 inhibition - 0.6429 64.29%
CYP2D6 inhibition - 0.9245 92.45%
CYP1A2 inhibition + 0.9600 96.00%
CYP2C8 inhibition + 0.4948 49.48%
CYP inhibitory promiscuity - 0.6796 67.96%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7071 70.71%
Carcinogenicity (trinary) Warning 0.4595 45.95%
Eye corrosion - 0.8863 88.63%
Eye irritation + 0.9961 99.61%
Skin irritation + 0.7297 72.97%
Skin corrosion - 0.9640 96.40%
Ames mutagenesis + 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8076 80.76%
Micronuclear - 0.6909 69.09%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.7001 70.01%
Acute Oral Toxicity (c) III 0.8093 80.93%
Estrogen receptor binding + 0.9370 93.70%
Androgen receptor binding + 0.9563 95.63%
Thyroid receptor binding + 0.7512 75.12%
Glucocorticoid receptor binding + 0.7718 77.18%
Aromatase binding + 0.8584 85.84%
PPAR gamma + 0.9060 90.60%
Honey bee toxicity - 0.9476 94.76%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9206 92.06%

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 97.65% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.71% 95.56%
CHEMBL242 Q92731 Estrogen receptor beta 86.98% 98.35%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.61% 94.62%
CHEMBL2535 P11166 Glucose transporter 84.34% 98.75%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 80.61% 94.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.43% 86.33%

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.
Tripterygium wilfordii

Cross-Links

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PubChem 69061
LOTUS LTS0170541
wikiData Q27109246