(1S,11R,12S)-15-methoxy-1-methyl-5,7-dioxa-1-azoniapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaene-11,16-diol

Details

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Internal ID 3c1e8f39-6922-4245-816b-c243855e61b9
Taxonomy Organoheterocyclic compounds > Tetrahydroisoquinolines
IUPAC Name (1S,11R,12S)-15-methoxy-1-methyl-5,7-dioxa-1-azoniapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaene-11,16-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H19NO5/c1-20-4-3-10-5-14(21)15(23-2)6-11(10)18(20)19(22)12-7-16-17(8-13(12)20)25-9-24-16/h5-8,18-19,22H,3-4,9H2,1-2H3/p+1/t18-,19+,20+/m0/s1
InChI Key CVCLYISJHIEWIH-XUVXKRRUSA-O
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H20NO5+
Molecular Weight 342.40 g/mol
Exact Mass 342.13414774 g/mol
Topological Polar Surface Area (TPSA) 68.20 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.41
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,11R,12S)-15-methoxy-1-methyl-5,7-dioxa-1-azoniapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaene-11,16-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9802 98.02%
Caco-2 + 0.6460 64.60%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Lysosomes 0.4547 45.47%
OATP2B1 inhibitior - 0.8568 85.68%
OATP1B1 inhibitior + 0.8786 87.86%
OATP1B3 inhibitior + 0.9451 94.51%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7568 75.68%
P-glycoprotein inhibitior - 0.5451 54.51%
P-glycoprotein substrate - 0.7976 79.76%
CYP3A4 substrate + 0.5986 59.86%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate + 0.3781 37.81%
CYP3A4 inhibition - 0.6193 61.93%
CYP2C9 inhibition - 0.8197 81.97%
CYP2C19 inhibition - 0.6367 63.67%
CYP2D6 inhibition + 0.6115 61.15%
CYP1A2 inhibition - 0.6567 65.67%
CYP2C8 inhibition - 0.5825 58.25%
CYP inhibitory promiscuity - 0.5601 56.01%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5638 56.38%
Eye corrosion - 0.9857 98.57%
Eye irritation - 0.8638 86.38%
Skin irritation - 0.7767 77.67%
Skin corrosion - 0.9329 93.29%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6103 61.03%
Micronuclear + 0.6800 68.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8501 85.01%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.6862 68.62%
Acute Oral Toxicity (c) III 0.6601 66.01%
Estrogen receptor binding + 0.8197 81.97%
Androgen receptor binding + 0.5650 56.50%
Thyroid receptor binding + 0.7730 77.30%
Glucocorticoid receptor binding + 0.7532 75.32%
Aromatase binding + 0.5799 57.99%
PPAR gamma + 0.7340 73.40%
Honey bee toxicity - 0.8152 81.52%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5549 55.49%
Fish aquatic toxicity + 0.7975 79.75%

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 98.08% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.84% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.45% 96.77%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 94.54% 82.67%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.90% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.90% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.10% 92.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.30% 85.14%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 88.44% 80.96%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.35% 92.94%
CHEMBL261 P00915 Carbonic anhydrase I 87.79% 96.76%
CHEMBL2581 P07339 Cathepsin D 86.74% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 86.74% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.55% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.48% 86.33%
CHEMBL213 P08588 Beta-1 adrenergic receptor 84.26% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.97% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.53% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.22% 93.99%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.98% 100.00%
CHEMBL2535 P11166 Glucose transporter 82.95% 98.75%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.30% 95.89%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.28% 89.62%
CHEMBL2413 P32246 C-C chemokine receptor type 1 82.00% 89.50%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.01% 93.40%
CHEMBL3438 Q05513 Protein kinase C zeta 80.40% 88.48%

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.
Cryptocarya phyllostemon
Hydrocotyle sibthorpioides

Cross-Links

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PubChem 163188143
LOTUS LTS0228335
wikiData Q105035987