1,2,3,4,5,7-Hexamethoxynaphthalene

Details

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Internal ID 880cf30e-1e5d-411d-989a-348a4e77a635
Taxonomy Benzenoids > Naphthalenes
IUPAC Name 1,2,3,4,5,7-hexamethoxynaphthalene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H20O6/c1-17-9-7-10-12(11(8-9)18-2)14(20-4)16(22-6)15(21-5)13(10)19-3/h7-8H,1-6H3
InChI Key LLVYASCUNDOCRV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20O6
Molecular Weight 308.33 g/mol
Exact Mass 308.12598835 g/mol
Topological Polar Surface Area (TPSA) 55.40 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.89
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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928035-91-0
DTXSID60853791
RefChem:71255
DTXCID70804532

2D Structure

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2D Structure of 1,2,3,4,5,7-Hexamethoxynaphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.7792 77.92%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.6311 63.11%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9496 94.96%
OATP1B3 inhibitior + 0.9843 98.43%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6838 68.38%
P-glycoprotein inhibitior - 0.8353 83.53%
P-glycoprotein substrate - 0.8914 89.14%
CYP3A4 substrate - 0.6320 63.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5092 50.92%
CYP3A4 inhibition - 0.5365 53.65%
CYP2C9 inhibition - 0.9304 93.04%
CYP2C19 inhibition - 0.6154 61.54%
CYP2D6 inhibition - 0.9262 92.62%
CYP1A2 inhibition + 0.9676 96.76%
CYP2C8 inhibition - 0.7731 77.31%
CYP inhibitory promiscuity + 0.6937 69.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8328 83.28%
Carcinogenicity (trinary) Non-required 0.4541 45.41%
Eye corrosion - 0.9691 96.91%
Eye irritation + 0.9100 91.00%
Skin irritation - 0.7476 74.76%
Skin corrosion - 0.9831 98.31%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4578 45.78%
Micronuclear + 0.5418 54.18%
Hepatotoxicity + 0.5335 53.35%
skin sensitisation - 0.8653 86.53%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.7460 74.60%
Acute Oral Toxicity (c) III 0.4055 40.55%
Estrogen receptor binding + 0.7371 73.71%
Androgen receptor binding - 0.6405 64.05%
Thyroid receptor binding + 0.6650 66.50%
Glucocorticoid receptor binding + 0.6187 61.87%
Aromatase binding + 0.6463 64.63%
PPAR gamma - 0.5212 52.12%
Honey bee toxicity - 0.8988 89.88%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.8400 84.00%
Fish aquatic toxicity + 0.9663 96.63%

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 91.29% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.08% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.69% 94.00%
CHEMBL2535 P11166 Glucose transporter 85.18% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.48% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.42% 96.00%
CHEMBL1907 P15144 Aminopeptidase N 83.28% 93.31%
CHEMBL4208 P20618 Proteasome component C5 80.99% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.44% 86.33%

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.
Frankenia thymifolia

Cross-Links

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PubChem 71445220
LOTUS LTS0036650
wikiData Q82848139