Mescengricin

Details

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Internal ID 8fda6f82-bc3e-48a2-9fe6-2a12acb3b46c
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Alpha carbolines
IUPAC Name [(2S)-2,3-dihydroxypropyl] 7-hydroxy-2-(4-hydroxy-2-methyl-6-oxo-2,3-dihydropyran-5-yl)-9H-pyrido[2,3-b]indole-4-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H20N2O8/c1-9-4-16(27)18(21(29)31-9)15-6-13(20(28)30-8-11(26)7-24)17-12-3-2-10(25)5-14(12)22-19(17)23-15/h2-3,5-6,9,11,24-27H,4,7-8H2,1H3,(H,22,23)/t9?,11-/m0/s1
InChI Key LIPSJRQTOKPVMQ-UMJHXOGRSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C21H20N2O8
Molecular Weight 428.40 g/mol
Exact Mass 428.12196560 g/mol
Topological Polar Surface Area (TPSA) 162.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.54
H-Bond Acceptor 9
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Mescengricin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9546 95.46%
Caco-2 - 0.8174 81.74%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.4575 45.75%
OATP2B1 inhibitior - 0.5741 57.41%
OATP1B1 inhibitior + 0.8616 86.16%
OATP1B3 inhibitior + 0.9443 94.43%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7257 72.57%
P-glycoprotein inhibitior - 0.6266 62.66%
P-glycoprotein substrate + 0.6880 68.80%
CYP3A4 substrate + 0.6539 65.39%
CYP2C9 substrate + 0.6060 60.60%
CYP2D6 substrate - 0.8712 87.12%
CYP3A4 inhibition - 0.8882 88.82%
CYP2C9 inhibition - 0.7058 70.58%
CYP2C19 inhibition - 0.7336 73.36%
CYP2D6 inhibition - 0.8801 88.01%
CYP1A2 inhibition - 0.5894 58.94%
CYP2C8 inhibition + 0.6529 65.29%
CYP inhibitory promiscuity - 0.7215 72.15%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5463 54.63%
Eye corrosion - 0.9870 98.70%
Eye irritation - 0.8645 86.45%
Skin irritation - 0.8042 80.42%
Skin corrosion - 0.9386 93.86%
Ames mutagenesis - 0.5137 51.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6823 68.23%
Micronuclear + 0.7500 75.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.8479 84.79%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.9051 90.51%
Acute Oral Toxicity (c) III 0.6017 60.17%
Estrogen receptor binding + 0.7143 71.43%
Androgen receptor binding + 0.8234 82.34%
Thyroid receptor binding - 0.5500 55.00%
Glucocorticoid receptor binding + 0.7330 73.30%
Aromatase binding + 0.6428 64.28%
PPAR gamma + 0.5365 53.65%
Honey bee toxicity - 0.8464 84.64%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6850 68.50%
Fish aquatic toxicity + 0.7714 77.14%

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 97.68% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.28% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.09% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 96.81% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.14% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.49% 85.14%
CHEMBL213 P08588 Beta-1 adrenergic receptor 93.06% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.84% 99.23%
CHEMBL2535 P11166 Glucose transporter 92.83% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.28% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.05% 99.17%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 88.54% 96.21%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.30% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.03% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.41% 95.56%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.88% 93.03%
CHEMBL3401 O75469 Pregnane X receptor 85.18% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.10% 90.71%
CHEMBL3785 Q8TDS4 Hydroxycarboxylic acid receptor 2 82.63% 94.05%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 81.33% 92.67%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.72% 86.92%
CHEMBL1937 Q92769 Histone deacetylase 2 80.51% 94.75%
CHEMBL220 P22303 Acetylcholinesterase 80.20% 94.45%

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 135464337
LOTUS LTS0094070
wikiData Q105152329