Methyl 6-hydroxy-3,4-dimethoxy-10-nitrophenanthrene-1-carboxylate

Details

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Internal ID fad3da77-a329-4499-81cb-db9bd5ddab32
Taxonomy Benzenoids > Phenanthrenes and derivatives > Aristolochic acids and derivatives
IUPAC Name methyl 6-hydroxy-3,4-dimethoxy-10-nitrophenanthrene-1-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H15NO7/c1-24-14-8-12(18(21)26-3)15-13(19(22)23)6-9-4-5-10(20)7-11(9)16(15)17(14)25-2/h4-8,20H,1-3H3
InChI Key NYRWXSZXODTBSI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H15NO7
Molecular Weight 357.30 g/mol
Exact Mass 357.08485182 g/mol
Topological Polar Surface Area (TPSA) 111.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.41
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 6-hydroxy-3,4-dimethoxy-10-nitrophenanthrene-1-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9393 93.93%
Caco-2 + 0.8333 83.33%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5570 55.70%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8613 86.13%
OATP1B3 inhibitior + 0.9292 92.92%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6255 62.55%
P-glycoprotein inhibitior - 0.5700 57.00%
P-glycoprotein substrate - 0.6485 64.85%
CYP3A4 substrate + 0.5819 58.19%
CYP2C9 substrate - 0.7962 79.62%
CYP2D6 substrate - 0.8331 83.31%
CYP3A4 inhibition - 0.7569 75.69%
CYP2C9 inhibition - 0.7353 73.53%
CYP2C19 inhibition - 0.7167 71.67%
CYP2D6 inhibition - 0.9353 93.53%
CYP1A2 inhibition - 0.6790 67.90%
CYP2C8 inhibition + 0.8461 84.61%
CYP inhibitory promiscuity - 0.8027 80.27%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.5135 51.35%
Carcinogenicity (trinary) Non-required 0.4022 40.22%
Eye corrosion - 0.9805 98.05%
Eye irritation - 0.5956 59.56%
Skin irritation - 0.8206 82.06%
Skin corrosion - 0.9666 96.66%
Ames mutagenesis + 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7305 73.05%
Micronuclear + 0.9600 96.00%
Hepatotoxicity + 0.6659 66.59%
skin sensitisation - 0.9237 92.37%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6425 64.25%
Nephrotoxicity - 0.6448 64.48%
Acute Oral Toxicity (c) III 0.5898 58.98%
Estrogen receptor binding + 0.8066 80.66%
Androgen receptor binding + 0.6430 64.30%
Thyroid receptor binding + 0.5992 59.92%
Glucocorticoid receptor binding + 0.8239 82.39%
Aromatase binding - 0.5627 56.27%
PPAR gamma + 0.7276 72.76%
Honey bee toxicity - 0.9268 92.68%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9910 99.10%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.31% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 94.32% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.65% 99.17%
CHEMBL2535 P11166 Glucose transporter 93.35% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.72% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.36% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.07% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.30% 94.00%
CHEMBL2581 P07339 Cathepsin D 84.10% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.86% 95.56%
CHEMBL4208 P20618 Proteasome component C5 81.16% 90.00%

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.
Aristolochia zollingeriana

Cross-Links

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PubChem 9975595
LOTUS LTS0037028
wikiData Q105187646