Flavanthrinin

Details

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Internal ID 1b05c734-ef16-454a-9d87-4c1a56993c29
Taxonomy Benzenoids > Phenanthrenes and derivatives > Phenanthrols
IUPAC Name 4-methoxyphenanthrene-2,7-diol
SMILES (Canonical) COC1=C2C(=CC(=C1)O)C=CC3=C2C=CC(=C3)O
SMILES (Isomeric) COC1=C2C(=CC(=C1)O)C=CC3=C2C=CC(=C3)O
InChI InChI=1S/C15H12O3/c1-18-14-8-12(17)7-10-3-2-9-6-11(16)4-5-13(9)15(10)14/h2-8,16-17H,1H3
InChI Key CJYQJCATAOEZRC-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O3
Molecular Weight 240.25 g/mol
Exact Mass 240.078644241 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.41
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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130827-45-1
4-methoxyphenanthrene-2,7-diol
CHEMBL447210
2,7-dihydroxy-4-methoxyphenanthrene
AKOS040762938

2D Structure

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2D Structure of Flavanthrinin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.7889 78.89%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7458 74.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8976 89.76%
OATP1B3 inhibitior + 0.9844 98.44%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6490 64.90%
P-glycoprotein inhibitior - 0.8941 89.41%
P-glycoprotein substrate - 0.7231 72.31%
CYP3A4 substrate - 0.6112 61.12%
CYP2C9 substrate - 0.7933 79.33%
CYP2D6 substrate + 0.4916 49.16%
CYP3A4 inhibition - 0.8396 83.96%
CYP2C9 inhibition - 0.6087 60.87%
CYP2C19 inhibition + 0.6820 68.20%
CYP2D6 inhibition - 0.9039 90.39%
CYP1A2 inhibition + 0.9713 97.13%
CYP2C8 inhibition + 0.6721 67.21%
CYP inhibitory promiscuity + 0.5370 53.70%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6786 67.86%
Carcinogenicity (trinary) Warning 0.4842 48.42%
Eye corrosion - 0.9716 97.16%
Eye irritation + 0.9898 98.98%
Skin irritation - 0.5423 54.23%
Skin corrosion - 0.9577 95.77%
Ames mutagenesis + 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6493 64.93%
Micronuclear - 0.5241 52.41%
Hepatotoxicity - 0.5291 52.91%
skin sensitisation - 0.8474 84.74%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6347 63.47%
Acute Oral Toxicity (c) III 0.7381 73.81%
Estrogen receptor binding + 0.9220 92.20%
Androgen receptor binding + 0.8682 86.82%
Thyroid receptor binding + 0.6429 64.29%
Glucocorticoid receptor binding + 0.8512 85.12%
Aromatase binding + 0.8229 82.29%
PPAR gamma + 0.7634 76.34%
Honey bee toxicity - 0.9338 93.38%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.7351 73.51%
Fish aquatic toxicity + 0.8679 86.79%

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 94.78% 91.11%
CHEMBL242 Q92731 Estrogen receptor beta 90.16% 98.35%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.75% 94.45%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 89.45% 89.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.89% 94.00%
CHEMBL2535 P11166 Glucose transporter 87.93% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.96% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.38% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.00% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 84.80% 90.20%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.44% 95.56%
CHEMBL4208 P20618 Proteasome component C5 82.13% 90.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.82% 92.94%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 80.02% 91.79%

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.
Agrostophyllum brevipes
Bletilla striata
Bulbophyllum reptans
Bulbophyllum vaginatum
Cremastra appendiculata
Dendrobium nobile
Dioscorea bulbifera
Pinalia acervata
Pleione bulbocodioides
Pleione yunnanensis
Sophora tomentosa
Syzygium aromaticum

Cross-Links

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PubChem 14777892
NPASS NPC53781
LOTUS LTS0027244
wikiData Q104961946