Morusignin J

Details

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Internal ID cf911cfa-889a-4841-8f56-451e050e82fc
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 6,8,11-trihydroxy-3,3-dimethyl-5-(3-methylbut-2-enyl)pyrano[2,3-c]xanthen-7-one
SMILES (Canonical) CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(C=CC(=C4O3)O)O)C=CC(O2)(C)C)C
SMILES (Isomeric) CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(C=CC(=C4O3)O)O)C=CC(O2)(C)C)C
InChI InChI=1S/C23H22O6/c1-11(2)5-6-12-18(26)17-19(27)16-14(24)7-8-15(25)22(16)28-21(17)13-9-10-23(3,4)29-20(12)13/h5,7-10,24-26H,6H2,1-4H3
InChI Key UTJUCKQNRWMQHF-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H22O6
Molecular Weight 394.40 g/mol
Exact Mass 394.14163842 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.76
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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CHEMBL2147812

2D Structure

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2D Structure of Morusignin J

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 - 0.6390 63.90%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6958 69.58%
OATP2B1 inhibitior - 0.5638 56.38%
OATP1B1 inhibitior + 0.8939 89.39%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8828 88.28%
P-glycoprotein inhibitior + 0.6340 63.40%
P-glycoprotein substrate - 0.6406 64.06%
CYP3A4 substrate + 0.5878 58.78%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate - 0.8144 81.44%
CYP3A4 inhibition - 0.8783 87.83%
CYP2C9 inhibition + 0.8399 83.99%
CYP2C19 inhibition + 0.8610 86.10%
CYP2D6 inhibition - 0.8178 81.78%
CYP1A2 inhibition - 0.5684 56.84%
CYP2C8 inhibition + 0.4609 46.09%
CYP inhibitory promiscuity + 0.7222 72.22%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6701 67.01%
Eye corrosion - 0.9913 99.13%
Eye irritation + 0.6167 61.67%
Skin irritation - 0.6990 69.90%
Skin corrosion - 0.9252 92.52%
Ames mutagenesis + 0.7036 70.36%
Human Ether-a-go-go-Related Gene inhibition - 0.4104 41.04%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.5824 58.24%
skin sensitisation - 0.6445 64.45%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.5641 56.41%
Acute Oral Toxicity (c) III 0.7034 70.34%
Estrogen receptor binding + 0.9112 91.12%
Androgen receptor binding + 0.7277 72.77%
Thyroid receptor binding + 0.6751 67.51%
Glucocorticoid receptor binding + 0.9174 91.74%
Aromatase binding + 0.7074 70.74%
PPAR gamma + 0.9104 91.04%
Honey bee toxicity - 0.7779 77.79%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9905 99.05%

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 99.70% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.38% 94.45%
CHEMBL2581 P07339 Cathepsin D 93.52% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 93.01% 91.49%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 92.98% 89.34%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.55% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 91.60% 94.73%
CHEMBL3038469 P24941 CDK2/Cyclin A 91.19% 91.38%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 90.29% 85.30%
CHEMBL221 P23219 Cyclooxygenase-1 89.30% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.28% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.62% 86.33%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 84.21% 80.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.63% 99.15%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.99% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 80.49% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.41% 99.23%

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.
Garcinia dulcis
Morus alba
Morus insignis

Cross-Links

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PubChem 71452951
NPASS NPC204290
LOTUS LTS0017929
wikiData Q104399153