1,2,3,4-Tetrahydronaphthalene-1,2,4,5-tetrol

Details

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Internal ID 556e53b9-542f-48b1-b694-8edc8bebd805
Taxonomy Benzenoids > Tetralins
IUPAC Name 1,2,3,4-tetrahydronaphthalene-1,2,4,5-tetrol
SMILES (Canonical) C1C(C(C2=C(C1O)C(=CC=C2)O)O)O
SMILES (Isomeric) C1C(C(C2=C(C1O)C(=CC=C2)O)O)O
InChI InChI=1S/C10H12O4/c11-6-3-1-2-5-9(6)7(12)4-8(13)10(5)14/h1-3,7-8,10-14H,4H2
InChI Key GRSZSHKSGISVFX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O4
Molecular Weight 196.20 g/mol
Exact Mass 196.07355886 g/mol
Topological Polar Surface Area (TPSA) 80.90 Ų
XlogP -0.60
Atomic LogP (AlogP) 0.22
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,2,3,4-Tetrahydronaphthalene-1,2,4,5-tetrol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9394 93.94%
Caco-2 - 0.8454 84.54%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.4553 45.53%
OATP2B1 inhibitior - 0.8600 86.00%
OATP1B1 inhibitior + 0.9554 95.54%
OATP1B3 inhibitior + 0.9705 97.05%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9777 97.77%
P-glycoprotein inhibitior - 0.9819 98.19%
P-glycoprotein substrate - 0.8580 85.80%
CYP3A4 substrate - 0.5729 57.29%
CYP2C9 substrate - 0.7510 75.10%
CYP2D6 substrate + 0.4329 43.29%
CYP3A4 inhibition - 0.8443 84.43%
CYP2C9 inhibition - 0.8731 87.31%
CYP2C19 inhibition - 0.8896 88.96%
CYP2D6 inhibition - 0.8397 83.97%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.7897 78.97%
CYP inhibitory promiscuity - 0.8582 85.82%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.4603 46.03%
Eye corrosion - 0.9820 98.20%
Eye irritation - 0.5926 59.26%
Skin irritation + 0.6353 63.53%
Skin corrosion - 0.8052 80.52%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7502 75.02%
Micronuclear + 0.6418 64.18%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.6505 65.05%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6608 66.08%
Acute Oral Toxicity (c) III 0.5779 57.79%
Estrogen receptor binding - 0.7625 76.25%
Androgen receptor binding - 0.5748 57.48%
Thyroid receptor binding - 0.5661 56.61%
Glucocorticoid receptor binding - 0.6150 61.50%
Aromatase binding - 0.9138 91.38%
PPAR gamma + 0.5177 51.77%
Honey bee toxicity - 0.9397 93.97%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.8161 81.61%

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 93.99% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.48% 93.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.75% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.17% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.97% 95.56%
CHEMBL2581 P07339 Cathepsin D 85.71% 98.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 74927835
LOTUS LTS0182394
wikiData Q104167430