Methyl 18-hydroxy-7-methoxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4(9),5,7-tetraene-19-carboxylate

Details

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Internal ID a4c462be-4ff8-4911-bffb-8d42c81962de
Taxonomy Alkaloids and derivatives > Yohimbine alkaloids
IUPAC Name methyl 18-hydroxy-7-methoxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4(9),5,7-tetraene-19-carboxylate
SMILES (Canonical) CC1C2CN3CCC4=C(C3CC2C(C(O1)O)C(=O)OC)NC5=C4C=C(C=C5)OC
SMILES (Isomeric) CC1C2CN3CCC4=C(C3CC2C(C(O1)O)C(=O)OC)NC5=C4C=C(C=C5)OC
InChI InChI=1S/C22H28N2O5/c1-11-16-10-24-7-6-13-14-8-12(27-2)4-5-17(14)23-20(13)18(24)9-15(16)19(21(25)28-3)22(26)29-11/h4-5,8,11,15-16,18-19,22-23,26H,6-7,9-10H2,1-3H3
InChI Key FXRNMKCIMCLQAT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H28N2O5
Molecular Weight 400.50 g/mol
Exact Mass 400.19982200 g/mol
Topological Polar Surface Area (TPSA) 84.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.24
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 18-hydroxy-7-methoxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4(9),5,7-tetraene-19-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8725 87.25%
Caco-2 + 0.7505 75.05%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.4771 47.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8616 86.16%
OATP1B3 inhibitior + 0.8473 84.73%
MATE1 inhibitior - 0.7237 72.37%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.8345 83.45%
P-glycoprotein inhibitior - 0.5827 58.27%
P-glycoprotein substrate + 0.7400 74.00%
CYP3A4 substrate + 0.6890 68.90%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7070 70.70%
CYP3A4 inhibition - 0.6133 61.33%
CYP2C9 inhibition - 0.8702 87.02%
CYP2C19 inhibition - 0.8779 87.79%
CYP2D6 inhibition - 0.7242 72.42%
CYP1A2 inhibition - 0.6598 65.98%
CYP2C8 inhibition - 0.6183 61.83%
CYP inhibitory promiscuity - 0.7236 72.36%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6364 63.64%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9871 98.71%
Skin irritation - 0.7944 79.44%
Skin corrosion - 0.9531 95.31%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6856 68.56%
Micronuclear + 0.5600 56.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8937 89.37%
Respiratory toxicity + 0.9444 94.44%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity - 0.5856 58.56%
Acute Oral Toxicity (c) II 0.6096 60.96%
Estrogen receptor binding + 0.7002 70.02%
Androgen receptor binding + 0.7452 74.52%
Thyroid receptor binding + 0.5606 56.06%
Glucocorticoid receptor binding + 0.5552 55.52%
Aromatase binding - 0.7323 73.23%
PPAR gamma - 0.6117 61.17%
Honey bee toxicity - 0.8320 83.20%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8947 89.47%

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 99.32% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.87% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.10% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.58% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.62% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.08% 97.09%
CHEMBL2535 P11166 Glucose transporter 90.59% 98.75%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.74% 92.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.82% 99.17%
CHEMBL4208 P20618 Proteasome component C5 87.58% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.45% 94.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.55% 96.77%
CHEMBL1951 P21397 Monoamine oxidase A 85.06% 91.49%
CHEMBL5747 Q92793 CREB-binding protein 84.66% 95.12%
CHEMBL340 P08684 Cytochrome P450 3A4 83.31% 91.19%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 82.74% 90.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.18% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.14% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.96% 99.23%
CHEMBL2581 P07339 Cathepsin D 80.89% 98.95%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.66% 95.89%
CHEMBL255 P29275 Adenosine A2b receptor 80.12% 98.59%

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.
Rauvolfia volkensii

Cross-Links

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PubChem 163049844
LOTUS LTS0240349
wikiData Q105004181