(3R)-8-hydroxy-3-(hydroxymethyl)-3-methyl-2H-naphthalene-1,4-dione

Details

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Internal ID 41e15e9c-4663-43fe-aeb4-e44ee0461549
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name (3R)-8-hydroxy-3-(hydroxymethyl)-3-methyl-2H-naphthalene-1,4-dione
SMILES (Canonical) CC1(CC(=O)C2=C(C1=O)C=CC=C2O)CO
SMILES (Isomeric) C[C@@]1(CC(=O)C2=C(C1=O)C=CC=C2O)CO
InChI InChI=1S/C12H12O4/c1-12(6-13)5-9(15)10-7(11(12)16)3-2-4-8(10)14/h2-4,13-14H,5-6H2,1H3/t12-/m1/s1
InChI Key NZGUHHPFWBHXCA-GFCCVEGCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H12O4
Molecular Weight 220.22 g/mol
Exact Mass 220.07355886 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.16
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R)-8-hydroxy-3-(hydroxymethyl)-3-methyl-2H-naphthalene-1,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9871 98.71%
Caco-2 + 0.7439 74.39%
Blood Brain Barrier - 0.6865 68.65%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.8691 86.91%
OATP2B1 inhibitior - 0.8604 86.04%
OATP1B1 inhibitior + 0.9118 91.18%
OATP1B3 inhibitior + 0.9525 95.25%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8707 87.07%
P-glycoprotein inhibitior - 0.9924 99.24%
P-glycoprotein substrate - 0.8232 82.32%
CYP3A4 substrate - 0.5070 50.70%
CYP2C9 substrate - 0.8004 80.04%
CYP2D6 substrate - 0.8297 82.97%
CYP3A4 inhibition - 0.7622 76.22%
CYP2C9 inhibition - 0.6270 62.70%
CYP2C19 inhibition - 0.6512 65.12%
CYP2D6 inhibition - 0.9006 90.06%
CYP1A2 inhibition + 0.7370 73.70%
CYP2C8 inhibition - 0.9200 92.00%
CYP inhibitory promiscuity - 0.7792 77.92%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8187 81.87%
Carcinogenicity (trinary) Non-required 0.5520 55.20%
Eye corrosion - 0.9884 98.84%
Eye irritation + 0.7412 74.12%
Skin irritation - 0.7163 71.63%
Skin corrosion - 0.9379 93.79%
Ames mutagenesis + 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8883 88.83%
Micronuclear - 0.6382 63.82%
Hepatotoxicity + 0.6282 62.82%
skin sensitisation - 0.8211 82.11%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.8795 87.95%
Acute Oral Toxicity (c) III 0.5629 56.29%
Estrogen receptor binding - 0.7513 75.13%
Androgen receptor binding + 0.6067 60.67%
Thyroid receptor binding - 0.7154 71.54%
Glucocorticoid receptor binding - 0.5435 54.35%
Aromatase binding - 0.8066 80.66%
PPAR gamma + 0.5576 55.76%
Honey bee toxicity - 0.9534 95.34%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9515 95.15%

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 97.58% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.06% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.75% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.44% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.52% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 87.43% 94.75%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.96% 82.69%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.50% 99.23%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.95% 90.24%
CHEMBL1951 P21397 Monoamine oxidase A 81.82% 91.49%
CHEMBL4208 P20618 Proteasome component C5 81.18% 90.00%
CHEMBL2996 Q05655 Protein kinase C delta 80.26% 97.79%

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.
Dionaea muscipula
Diospyros wallichii

Cross-Links

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PubChem 101337388
LOTUS LTS0015677
wikiData Q105187910