19R-Hydroxytabersonine

Details

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Internal ID d81a89f0-a7ba-4caa-82b2-27ef4fe97b20
Taxonomy Alkaloids and derivatives > Plumeran-type alkaloids
IUPAC Name methyl (1R,12S,19R)-12-[(1R)-1-hydroxyethyl]-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9,13-pentaene-10-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H24N2O3/c1-13(24)20-8-5-10-23-11-9-21(19(20)23)15-6-3-4-7-16(15)22-17(21)14(12-20)18(25)26-2/h3-8,13,19,22,24H,9-12H2,1-2H3/t13-,19+,20+,21+/m1/s1
InChI Key XDGRXQNYJMQLPU-VLCNGCBASA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C21H24N2O3
Molecular Weight 352.40 g/mol
Exact Mass 352.17869263 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.19
H-Bond Acceptor 5
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 19R-Hydroxytabersonine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9310 93.10%
Caco-2 + 0.7372 73.72%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8046 80.46%
OATP2B1 inhibitior - 0.8577 85.77%
OATP1B1 inhibitior + 0.9131 91.31%
OATP1B3 inhibitior + 0.9392 93.92%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7933 79.33%
P-glycoprotein inhibitior - 0.7977 79.77%
P-glycoprotein substrate + 0.6971 69.71%
CYP3A4 substrate + 0.6819 68.19%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8253 82.53%
CYP3A4 inhibition - 0.8185 81.85%
CYP2C9 inhibition - 0.7447 74.47%
CYP2C19 inhibition - 0.8660 86.60%
CYP2D6 inhibition + 0.5988 59.88%
CYP1A2 inhibition - 0.5879 58.79%
CYP2C8 inhibition - 0.6970 69.70%
CYP inhibitory promiscuity - 0.7798 77.98%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6264 62.64%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.9971 99.71%
Skin irritation - 0.7663 76.63%
Skin corrosion - 0.9293 92.93%
Ames mutagenesis - 0.6370 63.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4653 46.53%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.6064 60.64%
skin sensitisation - 0.8281 82.81%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.5642 56.42%
Acute Oral Toxicity (c) III 0.5336 53.36%
Estrogen receptor binding - 0.4918 49.18%
Androgen receptor binding + 0.6332 63.32%
Thyroid receptor binding - 0.5544 55.44%
Glucocorticoid receptor binding + 0.7298 72.98%
Aromatase binding + 0.5663 56.63%
PPAR gamma + 0.5890 58.90%
Honey bee toxicity - 0.8936 89.36%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9648 96.48%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.46% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.19% 96.09%
CHEMBL240 Q12809 HERG 97.98% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.72% 91.11%
CHEMBL4208 P20618 Proteasome component C5 95.88% 90.00%
CHEMBL2581 P07339 Cathepsin D 92.78% 98.95%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 91.99% 93.03%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.90% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.76% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 89.96% 90.17%
CHEMBL3524 P56524 Histone deacetylase 4 89.18% 92.97%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.65% 90.71%
CHEMBL5028 O14672 ADAM10 83.77% 97.50%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.71% 100.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.52% 91.07%
CHEMBL2535 P11166 Glucose transporter 83.49% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.42% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.26% 95.56%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 82.39% 91.65%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.94% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.46% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.51% 97.25%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.27% 97.14%

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.
Catharanthus ovalis
Catharanthus roseus

Cross-Links

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PubChem 57506202
LOTUS LTS0008750
wikiData Q105325694