Sinapiquinone

Details

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Internal ID 45e4b3c4-748b-4be1-92a7-7b9fdb295818
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name 1,8-dihydroxy-2-(10-hydroxy-5,7-dimethoxy-2-methyl-3,4-dioxoanthracen-9-yl)-3-methoxy-6-methylanthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C33H24O10/c1-12-6-17-23(19(34)7-12)30(37)26-18(29(17)36)11-21(43-5)27(32(26)39)22-15-8-13(2)28(35)33(40)25(15)31(38)24-16(22)9-14(41-3)10-20(24)42-4/h6-11,34,38-39H,1-5H3
InChI Key VKPISDBLFKLCMY-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C33H24O10
Molecular Weight 580.50 g/mol
Exact Mass 580.13694696 g/mol
Topological Polar Surface Area (TPSA) 157.00 Ų
XlogP 6.00
Atomic LogP (AlogP) 4.90
H-Bond Acceptor 10
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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DTXSID901037360
270256-41-2

2D Structure

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2D Structure of Sinapiquinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 - 0.7083 70.83%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7961 79.61%
OATP2B1 inhibitior - 0.8605 86.05%
OATP1B1 inhibitior + 0.8795 87.95%
OATP1B3 inhibitior + 0.8477 84.77%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.9344 93.44%
P-glycoprotein inhibitior + 0.7603 76.03%
P-glycoprotein substrate - 0.6684 66.84%
CYP3A4 substrate + 0.6411 64.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8261 82.61%
CYP3A4 inhibition - 0.6601 66.01%
CYP2C9 inhibition + 0.6880 68.80%
CYP2C19 inhibition + 0.6353 63.53%
CYP2D6 inhibition - 0.8312 83.12%
CYP1A2 inhibition + 0.7974 79.74%
CYP2C8 inhibition + 0.6200 62.00%
CYP inhibitory promiscuity + 0.7513 75.13%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9117 91.17%
Carcinogenicity (trinary) Non-required 0.5108 51.08%
Eye corrosion - 0.9939 99.39%
Eye irritation - 0.8161 81.61%
Skin irritation - 0.7222 72.22%
Skin corrosion - 0.9653 96.53%
Ames mutagenesis + 0.7946 79.46%
Human Ether-a-go-go-Related Gene inhibition + 0.8018 80.18%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.5927 59.27%
skin sensitisation - 0.8290 82.90%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.5944 59.44%
Acute Oral Toxicity (c) III 0.4119 41.19%
Estrogen receptor binding + 0.8622 86.22%
Androgen receptor binding + 0.5741 57.41%
Thyroid receptor binding + 0.5937 59.37%
Glucocorticoid receptor binding + 0.7260 72.60%
Aromatase binding - 0.4826 48.26%
PPAR gamma + 0.6924 69.24%
Honey bee toxicity - 0.7718 77.18%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9953 99.53%

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 98.20% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.57% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 96.10% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.51% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.01% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.00% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.81% 99.23%
CHEMBL2581 P07339 Cathepsin D 90.83% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 88.96% 91.49%
CHEMBL4208 P20618 Proteasome component C5 88.83% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.62% 96.09%
CHEMBL2535 P11166 Glucose transporter 87.11% 98.75%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.28% 96.67%
CHEMBL2056 P21728 Dopamine D1 receptor 84.57% 91.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 84.40% 92.68%
CHEMBL340 P08684 Cytochrome P450 3A4 83.73% 91.19%
CHEMBL1937 Q92769 Histone deacetylase 2 82.96% 94.75%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.77% 96.21%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.83% 95.89%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 80.67% 91.79%
CHEMBL3401 O75469 Pregnane X receptor 80.39% 94.73%

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 101013144
LOTUS LTS0246061
wikiData Q77510100