1,2,3-Trimethoxy-naphthalene

Details

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Internal ID de5b35d0-b037-4400-abf5-ee97f2794f47
Taxonomy Benzenoids > Naphthalenes
IUPAC Name 1,2,3-trimethoxynaphthalene
SMILES (Canonical) COC1=CC2=CC=CC=C2C(=C1OC)OC
SMILES (Isomeric) COC1=CC2=CC=CC=C2C(=C1OC)OC
InChI InChI=1S/C13H14O3/c1-14-11-8-9-6-4-5-7-10(9)12(15-2)13(11)16-3/h4-8H,1-3H3
InChI Key RANYXVFYAIGDFE-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O3
Molecular Weight 218.25 g/mol
Exact Mass 218.094294304 g/mol
Topological Polar Surface Area (TPSA) 27.70 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.87
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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1,2,3-trimethoxynaphthalene
SCHEMBL2889415
DTXSID40424029
RANYXVFYAIGDFE-UHFFFAOYSA-N
5892-02-4

2D Structure

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2D Structure of 1,2,3-Trimethoxy-naphthalene

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 + 0.8437 84.37%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.7042 70.42%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9497 94.97%
OATP1B3 inhibitior + 0.9852 98.52%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6690 66.90%
P-glycoprotein inhibitior - 0.9506 95.06%
P-glycoprotein substrate - 0.9317 93.17%
CYP3A4 substrate - 0.5785 57.85%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5092 50.92%
CYP3A4 inhibition - 0.7878 78.78%
CYP2C9 inhibition - 0.9044 90.44%
CYP2C19 inhibition - 0.5382 53.82%
CYP2D6 inhibition - 0.9505 95.05%
CYP1A2 inhibition + 0.9695 96.95%
CYP2C8 inhibition + 0.6109 61.09%
CYP inhibitory promiscuity + 0.6700 67.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8328 83.28%
Carcinogenicity (trinary) Warning 0.4868 48.68%
Eye corrosion - 0.9541 95.41%
Eye irritation + 0.9463 94.63%
Skin irritation - 0.6578 65.78%
Skin corrosion - 0.9786 97.86%
Ames mutagenesis + 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4684 46.84%
Micronuclear + 0.5018 50.18%
Hepatotoxicity + 0.6409 64.09%
skin sensitisation - 0.8192 81.92%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.6839 68.39%
Acute Oral Toxicity (c) III 0.5761 57.61%
Estrogen receptor binding + 0.7022 70.22%
Androgen receptor binding + 0.6003 60.03%
Thyroid receptor binding - 0.6221 62.21%
Glucocorticoid receptor binding - 0.8027 80.27%
Aromatase binding + 0.5418 54.18%
PPAR gamma - 0.8527 85.27%
Honey bee toxicity - 0.9238 92.38%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.9900 99.00%
Fish aquatic toxicity + 0.9572 95.72%

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 95.37% 91.11%
CHEMBL2535 P11166 Glucose transporter 89.61% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.42% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.78% 94.00%
CHEMBL4302 P08183 P-glycoprotein 1 85.39% 92.98%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.29% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.38% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 82.73% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.22% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.08% 92.62%
CHEMBL1907 P15144 Aminopeptidase N 81.43% 93.31%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.00% 94.03%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.44% 96.09%

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.
Pseudomarsupidium decipiens
Wettsteinia inversa

Cross-Links

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PubChem 6431118
LOTUS LTS0188252
wikiData Q82236435