Schumagnin

Details

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Internal ID a2cbc4a6-9fb7-45a3-8144-6d4192b8a273
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Pyranochromenes
IUPAC Name (1S,13S)-9-hydroxy-5-methyl-4,12-dioxa-14-azatetracyclo[11.3.1.02,11.03,8]heptadeca-2(11),3(8),5,9-tetraen-7-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H15NO4/c1-7-4-9(17)14-10(18)6-11-13(15(14)19-7)8-2-3-16-12(5-8)20-11/h4,6,8,12,16,18H,2-3,5H2,1H3/t8-,12-/m0/s1
InChI Key QWWVTYSQQINRTE-UFBFGSQYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H15NO4
Molecular Weight 273.28 g/mol
Exact Mass 273.10010796 g/mol
Topological Polar Surface Area (TPSA) 67.80 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.99
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Schumagnin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9815 98.15%
Caco-2 + 0.5910 59.10%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7465 74.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9318 93.18%
OATP1B3 inhibitior + 0.9596 95.96%
MATE1 inhibitior - 0.6200 62.00%
OCT2 inhibitior - 0.7820 78.20%
BSEP inhibitior - 0.8924 89.24%
P-glycoprotein inhibitior - 0.8302 83.02%
P-glycoprotein substrate - 0.6714 67.14%
CYP3A4 substrate + 0.5645 56.45%
CYP2C9 substrate + 0.6171 61.71%
CYP2D6 substrate - 0.8333 83.33%
CYP3A4 inhibition - 0.9237 92.37%
CYP2C9 inhibition - 0.9432 94.32%
CYP2C19 inhibition - 0.7923 79.23%
CYP2D6 inhibition - 0.7093 70.93%
CYP1A2 inhibition - 0.5755 57.55%
CYP2C8 inhibition - 0.7415 74.15%
CYP inhibitory promiscuity - 0.9168 91.68%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6520 65.20%
Eye corrosion - 0.9928 99.28%
Eye irritation - 0.8149 81.49%
Skin irritation - 0.8054 80.54%
Skin corrosion - 0.9635 96.35%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6323 63.23%
Micronuclear + 0.5900 59.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8537 85.37%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7010 70.10%
Acute Oral Toxicity (c) III 0.6869 68.69%
Estrogen receptor binding - 0.5513 55.13%
Androgen receptor binding + 0.7454 74.54%
Thyroid receptor binding - 0.6171 61.71%
Glucocorticoid receptor binding + 0.5510 55.10%
Aromatase binding - 0.6704 67.04%
PPAR gamma + 0.6805 68.05%
Honey bee toxicity - 0.8906 89.06%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.7309 73.09%

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 94.26% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.20% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.40% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.08% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.39% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.99% 94.80%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.38% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 86.15% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.61% 94.45%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 85.57% 85.11%
CHEMBL2581 P07339 Cathepsin D 84.70% 98.95%
CHEMBL4530 P00488 Coagulation factor XIII 84.33% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 83.52% 94.73%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.02% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.57% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.95% 90.71%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.52% 96.21%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.31% 86.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.55% 93.04%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.35% 93.03%

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.
Schumanniophyton magnificum

Cross-Links

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PubChem 13892265
LOTUS LTS0181855
wikiData Q105229439