2,7-Dihydroxy-6-methyl-8-methoxy-1-naphthalenecarbaldehyde

Details

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Internal ID 2677f265-729e-4bd7-97ec-df01aa51650f
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name 2,7-dihydroxy-8-methoxy-6-methylnaphthalene-1-carbaldehyde
SMILES (Canonical) CC1=CC2=C(C(=C(C=C2)O)C=O)C(=C1O)OC
SMILES (Isomeric) CC1=CC2=C(C(=C(C=C2)O)C=O)C(=C1O)OC
InChI InChI=1S/C13H12O4/c1-7-5-8-3-4-10(15)9(6-14)11(8)13(17-2)12(7)16/h3-6,15-16H,1-2H3
InChI Key KCZYFSGCRGWJHZ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12O4
Molecular Weight 232.23 g/mol
Exact Mass 232.07355886 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.38
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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2,7-dihydroxy-6-methyl-8-methoxy-1-naphthalenecarbaldehyde

2D Structure

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2D Structure of 2,7-Dihydroxy-6-methyl-8-methoxy-1-naphthalenecarbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9921 99.21%
Caco-2 - 0.5801 58.01%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8258 82.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8208 82.08%
OATP1B3 inhibitior + 0.9612 96.12%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8842 88.42%
P-glycoprotein inhibitior - 0.9148 91.48%
P-glycoprotein substrate - 0.9537 95.37%
CYP3A4 substrate - 0.5962 59.62%
CYP2C9 substrate - 0.8097 80.97%
CYP2D6 substrate - 0.7962 79.62%
CYP3A4 inhibition - 0.6693 66.93%
CYP2C9 inhibition - 0.5949 59.49%
CYP2C19 inhibition + 0.6611 66.11%
CYP2D6 inhibition - 0.7863 78.63%
CYP1A2 inhibition + 0.9480 94.80%
CYP2C8 inhibition - 0.6110 61.10%
CYP inhibitory promiscuity + 0.5630 56.30%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8820 88.20%
Carcinogenicity (trinary) Non-required 0.5289 52.89%
Eye corrosion - 0.9696 96.96%
Eye irritation + 0.9581 95.81%
Skin irritation + 0.5158 51.58%
Skin corrosion - 0.9637 96.37%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7507 75.07%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8734 87.34%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6687 66.87%
Acute Oral Toxicity (c) III 0.4858 48.58%
Estrogen receptor binding + 0.8453 84.53%
Androgen receptor binding + 0.6907 69.07%
Thyroid receptor binding + 0.6553 65.53%
Glucocorticoid receptor binding + 0.7205 72.05%
Aromatase binding - 0.5209 52.09%
PPAR gamma + 0.5212 52.12%
Honey bee toxicity - 0.9488 94.88%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9664 96.64%

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
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 99.47% 98.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.39% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.36% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 91.49% 91.49%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.98% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.81% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 87.77% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.75% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.54% 96.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.03% 90.24%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 82.40% 80.78%
CHEMBL3194 P02766 Transthyretin 80.56% 90.71%
CHEMBL4208 P20618 Proteasome component C5 80.39% 90.00%
CHEMBL2581 P07339 Cathepsin D 80.26% 98.95%

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.
Abutilon theophrasti
Hibiscus syriacus

Cross-Links

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PubChem 9991528
NPASS NPC202419
LOTUS LTS0009287
wikiData Q105139040