Jusmicranthin

Details

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Internal ID 954f91ed-13b6-4d5e-94e5-3bd7649835a0
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name 10-(1,3-benzodioxol-5-yl)-9-hydroxy-9H-[2]benzofuro[6,5-g][1,3]benzodioxol-7-one
SMILES (Canonical) C1OC2=C(O1)C=C(C=C2)C3=C4C(=CC5=C3C(OC5=O)O)C=CC6=C4OCO6
SMILES (Isomeric) C1OC2=C(O1)C=C(C=C2)C3=C4C(=CC5=C3C(OC5=O)O)C=CC6=C4OCO6
InChI InChI=1S/C20H12O7/c21-19-11-5-9-2-4-13-18(26-8-24-13)16(9)15(17(11)20(22)27-19)10-1-3-12-14(6-10)25-7-23-12/h1-6,20,22H,7-8H2
InChI Key RXFWNFQXBZITHO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H12O7
Molecular Weight 364.30 g/mol
Exact Mass 364.05830272 g/mol
Topological Polar Surface Area (TPSA) 83.40 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.13
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Jusmicranthin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 - 0.5580 55.80%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7642 76.42%
OATP2B1 inhibitior - 0.8660 86.60%
OATP1B1 inhibitior + 0.8893 88.93%
OATP1B3 inhibitior + 0.9265 92.65%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8897 88.97%
P-glycoprotein inhibitior - 0.4458 44.58%
P-glycoprotein substrate - 0.9036 90.36%
CYP3A4 substrate + 0.5254 52.54%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8620 86.20%
CYP3A4 inhibition + 0.6222 62.22%
CYP2C9 inhibition + 0.7171 71.71%
CYP2C19 inhibition + 0.5644 56.44%
CYP2D6 inhibition - 0.5972 59.72%
CYP1A2 inhibition + 0.6685 66.85%
CYP2C8 inhibition - 0.6065 60.65%
CYP inhibitory promiscuity + 0.6092 60.92%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Warning 0.4234 42.34%
Eye corrosion - 0.9850 98.50%
Eye irritation - 0.5926 59.26%
Skin irritation - 0.6124 61.24%
Skin corrosion - 0.9662 96.62%
Ames mutagenesis + 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7345 73.45%
Micronuclear + 0.8774 87.74%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.7428 74.28%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.5989 59.89%
Acute Oral Toxicity (c) III 0.5805 58.05%
Estrogen receptor binding + 0.8425 84.25%
Androgen receptor binding + 0.7764 77.64%
Thyroid receptor binding + 0.6522 65.22%
Glucocorticoid receptor binding + 0.8561 85.61%
Aromatase binding + 0.6263 62.63%
PPAR gamma + 0.8803 88.03%
Honey bee toxicity - 0.8332 83.32%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9456 94.56%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.10% 96.77%
CHEMBL1951 P21397 Monoamine oxidase A 96.44% 91.49%
CHEMBL240 Q12809 HERG 94.43% 89.76%
CHEMBL2581 P07339 Cathepsin D 93.20% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.19% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.06% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.71% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 90.48% 94.80%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.37% 94.45%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.33% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.98% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.31% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.71% 99.23%
CHEMBL1929 P47989 Xanthine dehydrogenase 85.54% 96.12%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 84.60% 80.96%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 83.27% 95.78%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.27% 97.09%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 81.54% 95.53%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.15% 100.00%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 81.02% 82.67%
CHEMBL4530 P00488 Coagulation factor XIII 80.46% 96.00%

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.
Hypoestes purpurea

Cross-Links

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PubChem 101041139
NPASS NPC36256
LOTUS LTS0241001
wikiData Q105247001