Coeloginanthrin

Details

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Internal ID f0f4aef4-ce84-4de1-bd1a-9fb080addab0
Taxonomy Benzenoids > Phenanthrenes and derivatives > Phenanthrols
IUPAC Name 7,8-dimethoxyphenanthrene-2,4,6-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H14O5/c1-20-15-10-4-3-8-5-9(17)6-12(18)14(8)11(10)7-13(19)16(15)21-2/h3-7,17-19H,1-2H3
InChI Key RPXPLEKXBFYMQL-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O5
Molecular Weight 286.28 g/mol
Exact Mass 286.08412354 g/mol
Topological Polar Surface Area (TPSA) 79.20 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.13
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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7,8-dimethoxyphenanthrene-2,4,6-triol
RefChem:127393
382145-13-3
DTXSID101031837
3,5,7-trihydroxy-1,2-dimethoxyphenanthrene
Q17332620

2D Structure

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2D Structure of Coeloginanthrin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9755 97.55%
Caco-2 + 0.8630 86.30%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5988 59.88%
OATP2B1 inhibitior - 0.7137 71.37%
OATP1B1 inhibitior + 0.9188 91.88%
OATP1B3 inhibitior + 0.9514 95.14%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6320 63.20%
P-glycoprotein inhibitior - 0.8401 84.01%
P-glycoprotein substrate - 0.8529 85.29%
CYP3A4 substrate - 0.5658 56.58%
CYP2C9 substrate - 0.7933 79.33%
CYP2D6 substrate + 0.4916 49.16%
CYP3A4 inhibition - 0.5403 54.03%
CYP2C9 inhibition + 0.5152 51.52%
CYP2C19 inhibition + 0.6198 61.98%
CYP2D6 inhibition - 0.6838 68.38%
CYP1A2 inhibition + 0.9269 92.69%
CYP2C8 inhibition + 0.6215 62.15%
CYP inhibitory promiscuity + 0.7330 73.30%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5713 57.13%
Eye corrosion - 0.9725 97.25%
Eye irritation + 0.9113 91.13%
Skin irritation - 0.5648 56.48%
Skin corrosion - 0.8355 83.55%
Ames mutagenesis + 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3935 39.35%
Micronuclear + 0.6700 67.00%
Hepatotoxicity - 0.5178 51.78%
skin sensitisation - 0.7295 72.95%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.7531 75.31%
Acute Oral Toxicity (c) III 0.6266 62.66%
Estrogen receptor binding + 0.8150 81.50%
Androgen receptor binding + 0.5354 53.54%
Thyroid receptor binding + 0.7741 77.41%
Glucocorticoid receptor binding + 0.8187 81.87%
Aromatase binding + 0.7137 71.37%
PPAR gamma + 0.6299 62.99%
Honey bee toxicity - 0.9234 92.34%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity + 0.9407 94.07%

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 98.31% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 94.40% 91.49%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 93.63% 92.68%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.35% 94.45%
CHEMBL1929 P47989 Xanthine dehydrogenase 91.78% 96.12%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.35% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.15% 96.09%
CHEMBL242 Q92731 Estrogen receptor beta 87.11% 98.35%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.26% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.67% 99.17%
CHEMBL4208 P20618 Proteasome component C5 84.42% 90.00%
CHEMBL2535 P11166 Glucose transporter 84.21% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.24% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 82.05% 94.75%
CHEMBL2581 P07339 Cathepsin D 81.53% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.21% 93.99%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.80% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.02% 95.56%

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.
Coelogyne cristata

Cross-Links

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PubChem 10913128
NPASS NPC100449
LOTUS LTS0036856
wikiData Q17332620