Emestrin

Details

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Internal ID 703a7d34-2905-4213-afce-b5cf0cdb827c
Taxonomy Phenylpropanoids and polyketides > Macrolactams
IUPAC Name (1R,3S,9S,23S,24R,32R)-19,23,32-trihydroxy-15-methoxy-28-methyl-6,10,17-trioxa-25,26-dithia-2,28-diazaheptacyclo[22.2.2.11,4.12,24.112,16.118,22.03,9]dotriaconta-4,7,12(31),13,15,18,20,22(30)-octaene-11,27,29-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H22N2O10S2/c1-28-24(34)27-22(32)14-11-37-8-7-17-20(14)29(27)25(35)26(28,40-41-27)21(31)12-3-5-15(30)18(9-12)38-19-10-13(23(33)39-17)4-6-16(19)36-2/h3-11,17,20-22,30-32H,1-2H3/t17-,20-,21-,22+,26+,27+/m0/s1
InChI Key UWWYWUMDYAWTKK-YITDFDIYSA-N
Popularity 39 references in papers

Physical and Chemical Properties

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Molecular Formula C27H22N2O10S2
Molecular Weight 598.60 g/mol
Exact Mass 598.07158725 g/mol
Topological Polar Surface Area (TPSA) 206.00 Ų
XlogP -0.10
Atomic LogP (AlogP) 2.02
H-Bond Acceptor 12
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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(1R,3S,9S,23S,24R,32R)-19,23,32-trihydroxy-15-methoxy-28-methyl-6,10,17-trioxa-25,26-dithia-2,28-diazaheptacyclo[22.2.2.11,4.12,24.112,16.118,22.03,9]dotriaconta-4,7,12(31),13,15,18,20,22(30)-octaene-11,27,29-trione
97816-62-1
(1R,3S,9S,23S,24R,32R)-19,23,32-trihydroxy-15-methoxy-28-methyl-6,10,17-trioxa-25,26-dithia-2,28-diazaheptacyclo(22.2.2.11,4.12,24.112,16.118,22.03,9)dotriaconta-4,7,12(31),13,15,18,20,22(30)-octaene-11,27,29-trione
RefChem:136670
DTXCID601528520
20,24,32-trihydroxy-16-methoxy-29-methyl-6,10,18-trioxa-26,27-dithia-2,29-diazaheptacyclo(23.2.2.11,4.12,25.119,23.03,9.012,17)dotriaconta-4,7,12(17),13,15,19,21,23(31)-octaene-11,28,30-trione
DTXSID901046701
SCHEMBL1096344
CHEBI:198198

2D Structure

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2D Structure of Emestrin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6970 69.70%
Caco-2 - 0.8155 81.55%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.4645 46.45%
OATP2B1 inhibitior - 0.7158 71.58%
OATP1B1 inhibitior + 0.8819 88.19%
OATP1B3 inhibitior + 0.9310 93.10%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9580 95.80%
P-glycoprotein inhibitior + 0.7713 77.13%
P-glycoprotein substrate - 0.5000 50.00%
CYP3A4 substrate + 0.7055 70.55%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8247 82.47%
CYP3A4 inhibition - 0.7863 78.63%
CYP2C9 inhibition - 0.5663 56.63%
CYP2C19 inhibition - 0.5623 56.23%
CYP2D6 inhibition - 0.8035 80.35%
CYP1A2 inhibition - 0.6999 69.99%
CYP2C8 inhibition + 0.6887 68.87%
CYP inhibitory promiscuity - 0.6432 64.32%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5553 55.53%
Eye corrosion - 0.9826 98.26%
Eye irritation - 0.9139 91.39%
Skin irritation - 0.7653 76.53%
Skin corrosion - 0.9219 92.19%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5341 53.41%
Micronuclear + 0.8800 88.00%
Hepatotoxicity + 0.5679 56.79%
skin sensitisation - 0.8373 83.73%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.5945 59.45%
Acute Oral Toxicity (c) III 0.5837 58.37%
Estrogen receptor binding + 0.7861 78.61%
Androgen receptor binding + 0.7567 75.67%
Thyroid receptor binding + 0.6559 65.59%
Glucocorticoid receptor binding + 0.7740 77.40%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.7164 71.64%
Honey bee toxicity - 0.7233 72.33%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9874 98.74%

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
CHEMBL2581 P07339 Cathepsin D 96.18% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.12% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.99% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.40% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.76% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 93.51% 91.49%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.17% 99.15%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 93.05% 93.40%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.32% 89.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.21% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.56% 99.23%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.56% 86.92%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.65% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.34% 85.14%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 82.67% 95.78%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.57% 92.62%
CHEMBL3891 P07384 Calpain 1 81.19% 93.04%

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.
Zanthoxylum asiaticum

Cross-Links

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PubChem 11758256
NPASS NPC61564
LOTUS LTS0245357
wikiData Q75058803