Sch-42137-13-acetate

Details

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Internal ID de227ea2-e040-4c7a-8223-679f1eb18eb7
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name [(17S)-24-ethyl-3,10,28-trihydroxy-14-methoxy-25-methyl-5,26-dioxo-12,18,20-trioxa-25-azaheptacyclo[15.11.1.02,15.04,13.06,11.021,29.022,27]nonacosa-1(28),2(15),3,6(11),13,21(29),22(27),23-octaen-7-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H29NO11/c1-5-12-8-13-19(31(38)32(12)3)25(36)22-18-14(9-17-20(22)27(13)41-10-40-17)28(39-4)30-23(24(18)35)26(37)21-16(42-11(2)33)7-6-15(34)29(21)43-30/h8,15-17,34-36H,5-7,9-10H2,1-4H3/t15?,16?,17-/m0/s1
InChI Key LXIYUOHIQKKZGT-JCYILVPMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H29NO11
Molecular Weight 591.60 g/mol
Exact Mass 591.17406074 g/mol
Topological Polar Surface Area (TPSA) 161.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.69
H-Bond Acceptor 12
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Sch-42137-13-acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7008 70.08%
Caco-2 - 0.7937 79.37%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Nucleus 0.4427 44.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8337 83.37%
OATP1B3 inhibitior + 0.9149 91.49%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.6122 61.22%
P-glycoprotein inhibitior + 0.6752 67.52%
P-glycoprotein substrate + 0.7799 77.99%
CYP3A4 substrate + 0.6939 69.39%
CYP2C9 substrate + 0.7932 79.32%
CYP2D6 substrate - 0.8616 86.16%
CYP3A4 inhibition + 0.6579 65.79%
CYP2C9 inhibition - 0.8011 80.11%
CYP2C19 inhibition - 0.7319 73.19%
CYP2D6 inhibition - 0.8990 89.90%
CYP1A2 inhibition - 0.6989 69.89%
CYP2C8 inhibition + 0.6858 68.58%
CYP inhibitory promiscuity - 0.6888 68.88%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5819 58.19%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9207 92.07%
Skin irritation - 0.8181 81.81%
Skin corrosion - 0.9471 94.71%
Ames mutagenesis + 0.5828 58.28%
Human Ether-a-go-go-Related Gene inhibition - 0.4695 46.95%
Micronuclear + 0.6700 67.00%
Hepatotoxicity - 0.5145 51.45%
skin sensitisation - 0.8993 89.93%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.9341 93.41%
Acute Oral Toxicity (c) III 0.6722 67.22%
Estrogen receptor binding + 0.8134 81.34%
Androgen receptor binding + 0.7470 74.70%
Thyroid receptor binding + 0.5804 58.04%
Glucocorticoid receptor binding + 0.8293 82.93%
Aromatase binding + 0.6869 68.69%
PPAR gamma + 0.6463 64.63%
Honey bee toxicity - 0.6955 69.55%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.7666 76.66%

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 98.91% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.56% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.75% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.50% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.43% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.39% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 93.81% 92.62%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.99% 96.77%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.76% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.19% 86.33%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.91% 94.42%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.29% 95.56%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 85.64% 95.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.83% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.44% 99.17%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.87% 96.00%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 80.30% 90.95%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 80.21% 97.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139586908
LOTUS LTS0143011
wikiData Q77517319