Trigonostemone

Details

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Internal ID fe06a185-f61a-4ee6-8c59-47b496128adf
Taxonomy Benzenoids > Phenanthrenes and derivatives > Phenanthrols
IUPAC Name 3,6,9-trimethoxy-1,1,7-trimethylphenanthren-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H22O4/c1-11-7-14-12(8-16(11)22-4)13-9-18(24-6)19(21)20(2,3)15(13)10-17(14)23-5/h7-10H,1-6H3
InChI Key SVSYTLDPFSIEJY-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C20H22O4
Molecular Weight 326.40 g/mol
Exact Mass 326.15180918 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.01
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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RefChem:191655
3,6,9-trimethoxy-1,1,7-trimethylphenanthren-2-one
133084-24-9
CHEMBL1078766
SCHEMBL30750912
BDBM50446569

2D Structure

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2D Structure of Trigonostemone

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 + 0.8788 87.88%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.8069 80.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9171 91.71%
OATP1B3 inhibitior + 0.9761 97.61%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8260 82.60%
P-glycoprotein inhibitior - 0.4908 49.08%
P-glycoprotein substrate - 0.8193 81.93%
CYP3A4 substrate + 0.5606 56.06%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7685 76.85%
CYP3A4 inhibition + 0.9235 92.35%
CYP2C9 inhibition - 0.5954 59.54%
CYP2C19 inhibition + 0.8491 84.91%
CYP2D6 inhibition - 0.8225 82.25%
CYP1A2 inhibition + 0.8869 88.69%
CYP2C8 inhibition - 0.6410 64.10%
CYP inhibitory promiscuity + 0.8499 84.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9163 91.63%
Carcinogenicity (trinary) Non-required 0.4602 46.02%
Eye corrosion - 0.9865 98.65%
Eye irritation + 0.8172 81.72%
Skin irritation - 0.8136 81.36%
Skin corrosion - 0.9854 98.54%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4151 41.51%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.5302 53.02%
skin sensitisation - 0.7817 78.17%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.5914 59.14%
Acute Oral Toxicity (c) III 0.6333 63.33%
Estrogen receptor binding + 0.9118 91.18%
Androgen receptor binding + 0.5955 59.55%
Thyroid receptor binding + 0.7263 72.63%
Glucocorticoid receptor binding + 0.6432 64.32%
Aromatase binding + 0.7912 79.12%
PPAR gamma + 0.6829 68.29%
Honey bee toxicity - 0.8339 83.39%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9959 99.59%

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 96.80% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.07% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.57% 86.33%
CHEMBL2535 P11166 Glucose transporter 90.50% 98.75%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 86.32% 82.38%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.67% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.87% 94.45%
CHEMBL1907 P15144 Aminopeptidase N 84.74% 93.31%
CHEMBL1871 P10275 Androgen Receptor 83.87% 96.43%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.51% 92.94%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.33% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.97% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.81% 95.50%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.26% 93.99%
CHEMBL4208 P20618 Proteasome component C5 80.93% 90.00%
CHEMBL1937 Q92769 Histone deacetylase 2 80.31% 94.75%

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.
Byrsonima coccolobifolia
Strophioblachia fimbricalyx
Trigonostemon reidioides
Trigonostemon viridissimus var. elegantissimus

Cross-Links

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PubChem 14731300
NPASS NPC290601
ChEMBL CHEMBL1078766
LOTUS LTS0149728
wikiData Q104197716