2,2'-(Ethan-1,1-diyl)bis(3,5,6,7,8-pentahydroxy-1,4-naphthoquinone)

Details

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Internal ID 673e6abd-c78c-4fa6-b24e-0068503583cf
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 2,3,5,6,8-pentahydroxy-7-[1-(1,3,4,6,7-pentahydroxy-5,8-dioxonaphthalen-2-yl)ethyl]naphthalene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H14O14/c1-2(3-9(23)5-7(13(27)11(3)25)17(31)21(35)19(33)15(5)29)4-10(24)6-8(14(28)12(4)26)18(32)22(36)20(34)16(6)30/h2,23-28,33-36H,1H3
InChI Key QTMACIXHHMCXNS-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H14O14
Molecular Weight 502.30 g/mol
Exact Mass 502.03835512 g/mol
Topological Polar Surface Area (TPSA) 271.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 1.49
H-Bond Acceptor 14
H-Bond Donor 10
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,2'-(Ethan-1,1-diyl)bis(3,5,6,7,8-pentahydroxy-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 + 0.9797 97.97%
Caco-2 - 0.7888 78.88%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.6587 65.87%
OATP2B1 inhibitior + 0.5772 57.72%
OATP1B1 inhibitior + 0.8759 87.59%
OATP1B3 inhibitior + 0.9730 97.30%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9588 95.88%
BSEP inhibitior - 0.8333 83.33%
P-glycoprotein inhibitior - 0.7236 72.36%
P-glycoprotein substrate - 0.9752 97.52%
CYP3A4 substrate - 0.7027 70.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8667 86.67%
CYP3A4 inhibition - 0.6792 67.92%
CYP2C9 inhibition + 0.7953 79.53%
CYP2C19 inhibition - 0.8423 84.23%
CYP2D6 inhibition - 0.8379 83.79%
CYP1A2 inhibition + 0.8885 88.85%
CYP2C8 inhibition - 0.9932 99.32%
CYP inhibitory promiscuity + 0.5983 59.83%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8875 88.75%
Carcinogenicity (trinary) Non-required 0.5280 52.80%
Eye corrosion - 0.9928 99.28%
Eye irritation - 0.5080 50.80%
Skin irritation + 0.5787 57.87%
Skin corrosion - 0.7415 74.15%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7849 78.49%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.6889 68.89%
skin sensitisation + 0.6130 61.30%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.6521 65.21%
Acute Oral Toxicity (c) III 0.4478 44.78%
Estrogen receptor binding + 0.7516 75.16%
Androgen receptor binding - 0.6317 63.17%
Thyroid receptor binding - 0.5897 58.97%
Glucocorticoid receptor binding + 0.6519 65.19%
Aromatase binding - 0.6234 62.34%
PPAR gamma - 0.5060 50.60%
Honey bee toxicity - 0.8974 89.74%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9948 99.48%

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 94.31% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.82% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.82% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.45% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.07% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.79% 99.23%

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 135706818
LOTUS LTS0045215
wikiData Q105227804