Mutadione D

Details

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Internal ID 90c9cd03-02e4-4068-8bb0-fbeaf4ba8bd2
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 4',5,6-trihydroxy-4,5'-di(pentadecyl)spiro[1-benzofuran-3,2'-cyclopent-4-ene]-1',2,3'-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H66O7/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-32-36-35(31-34(43)37(32)44)49-41(48)42(36)39(46)33(38(45)40(42)47)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h31,43-45H,3-30H2,1-2H3
InChI Key FUYDUONXCBMQBL-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C42H66O7
Molecular Weight 683.00 g/mol
Exact Mass 682.48085444 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP 16.00
Atomic LogP (AlogP) 11.33
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 28

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Mutadione D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 - 0.8071 80.71%
Blood Brain Barrier - 0.5145 51.45%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.8306 83.06%
OATP2B1 inhibitior - 0.7126 71.26%
OATP1B1 inhibitior + 0.8442 84.42%
OATP1B3 inhibitior + 0.8806 88.06%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.7176 71.76%
P-glycoprotein inhibitior + 0.6547 65.47%
P-glycoprotein substrate - 0.7567 75.67%
CYP3A4 substrate + 0.5641 56.41%
CYP2C9 substrate - 0.6056 60.56%
CYP2D6 substrate - 0.8774 87.74%
CYP3A4 inhibition + 0.6183 61.83%
CYP2C9 inhibition - 0.5183 51.83%
CYP2C19 inhibition + 0.5550 55.50%
CYP2D6 inhibition - 0.8732 87.32%
CYP1A2 inhibition + 0.7768 77.68%
CYP2C8 inhibition + 0.5212 52.12%
CYP inhibitory promiscuity - 0.6748 67.48%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5566 55.66%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.6795 67.95%
Skin irritation - 0.5931 59.31%
Skin corrosion - 0.9051 90.51%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6332 63.32%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5964 59.64%
skin sensitisation - 0.7458 74.58%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.6718 67.18%
Acute Oral Toxicity (c) II 0.3680 36.80%
Estrogen receptor binding + 0.7622 76.22%
Androgen receptor binding + 0.7059 70.59%
Thyroid receptor binding - 0.6039 60.39%
Glucocorticoid receptor binding - 0.5180 51.80%
Aromatase binding - 0.5054 50.54%
PPAR gamma + 0.5700 57.00%
Honey bee toxicity - 0.9707 97.07%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.8086 80.86%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL230 P35354 Cyclooxygenase-2 98.43% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.28% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.03% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 94.38% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.84% 86.33%
CHEMBL240 Q12809 HERG 93.23% 89.76%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.32% 94.45%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.30% 92.08%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 88.82% 94.80%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.34% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.90% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.52% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.15% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.04% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.82% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.31% 95.56%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 82.58% 96.37%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.46% 96.95%
CHEMBL4581 P52732 Kinesin-like protein 1 82.36% 93.18%
CHEMBL1907 P15144 Aminopeptidase N 80.73% 93.31%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.38% 93.99%

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.
There are no matching plants.

Cross-Links

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PubChem 10532590
LOTUS LTS0022865
wikiData Q77510345