2-Hydroxy-1,4-naphthoquinone

Details

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Internal ID 11f7758f-47e9-4725-aa5e-0272295696fe
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 4-hydroxynaphthalene-1,2-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H6O3/c11-8-5-9(12)10(13)7-4-2-1-3-6(7)8/h1-5,11H
InChI Key WVCHIGAIXREVNS-UHFFFAOYSA-N
Popularity 1,600 references in papers

Physical and Chemical Properties

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Molecular Formula C10H6O3
Molecular Weight 174.15 g/mol
Exact Mass 174.031694049 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.35
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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2-Hydroxy-1,4-naphthoquinone
83-72-7
2-Hydroxynaphthoquinone
2-hydroxynaphthalene-1,4-dione
2-Hydroxy-1,4-naphoquinone
Henna
Mehendi
Lawson
Mendi
HANA
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Hydroxy-1,4-naphthoquinone

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 + 0.8663 86.63%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.7929 79.29%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9498 94.98%
OATP1B3 inhibitior + 0.9732 97.32%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9269 92.69%
P-glycoprotein inhibitior - 0.9690 96.90%
P-glycoprotein substrate - 0.9745 97.45%
CYP3A4 substrate - 0.6782 67.82%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8555 85.55%
CYP3A4 inhibition - 0.9078 90.78%
CYP2C9 inhibition + 0.7177 71.77%
CYP2C19 inhibition - 0.7624 76.24%
CYP2D6 inhibition - 0.8078 80.78%
CYP1A2 inhibition + 0.9206 92.06%
CYP2C8 inhibition - 0.9772 97.72%
CYP inhibitory promiscuity - 0.5311 53.11%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8592 85.92%
Carcinogenicity (trinary) Non-required 0.4980 49.80%
Eye corrosion - 0.9522 95.22%
Eye irritation + 0.9972 99.72%
Skin irritation + 0.8279 82.79%
Skin corrosion - 0.9571 95.71%
Ames mutagenesis + 0.6846 68.46%
Human Ether-a-go-go-Related Gene inhibition - 0.9237 92.37%
Micronuclear + 0.6049 60.49%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.8052 80.52%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.7649 76.49%
Acute Oral Toxicity (c) II 0.4042 40.42%
Estrogen receptor binding + 0.6406 64.06%
Androgen receptor binding + 0.6101 61.01%
Thyroid receptor binding + 0.5211 52.11%
Glucocorticoid receptor binding - 0.5896 58.96%
Aromatase binding - 0.5328 53.28%
PPAR gamma + 0.6212 62.12%
Honey bee toxicity - 0.8574 85.74%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9762 97.62%

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
CHEMBL2581 P07339 Cathepsin D 95.41% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.92% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.19% 95.56%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 91.74% 85.94%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 88.87% 96.67%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.91% 82.69%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.24% 99.23%
CHEMBL2535 P11166 Glucose transporter 80.48% 98.75%
CHEMBL1951 P21397 Monoamine oxidase A 80.09% 91.49%

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.
Impatiens balsamina
Impatiens noli-tangere
Lawsonia inermis
Lomatia ferruginea

Cross-Links

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PubChem 6755
LOTUS LTS0266331
wikiData Q104392899