Tabernine A

Details

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Internal ID e533c8be-9254-4422-b29f-ef796907c48e
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Beta carbolines
IUPAC Name 6,8-dimethyl-5,7,17-triazatetracyclo[8.7.0.02,7.011,16]heptadeca-1,8,10,12,14,16-hexaene
SMILES (Canonical) CC1NCCC2=C3C(=C4C=CC=CC4=N3)C=C(N12)C
SMILES (Isomeric) CC1NCCC2=C3C(=C4C=CC=CC4=N3)C=C(N12)C
InChI InChI=1S/C16H17N3/c1-10-9-13-12-5-3-4-6-14(12)18-16(13)15-7-8-17-11(2)19(10)15/h3-6,9,11,17H,7-8H2,1-2H3
InChI Key VBMLQDYYOPHOCB-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H17N3
Molecular Weight 251.33 g/mol
Exact Mass 251.142247555 g/mol
Topological Polar Surface Area (TPSA) 29.80 Ų
XlogP 2.40
Atomic LogP (AlogP) 3.11
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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CHEMBL555046

2D Structure

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2D Structure of Tabernine A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.7432 74.32%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.6772 67.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9374 93.74%
OATP1B3 inhibitior + 0.9457 94.57%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior + 0.6250 62.50%
BSEP inhibitior + 0.6075 60.75%
P-glycoprotein inhibitior - 0.9160 91.60%
P-glycoprotein substrate - 0.7661 76.61%
CYP3A4 substrate + 0.5505 55.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8029 80.29%
CYP3A4 inhibition - 0.7587 75.87%
CYP2C9 inhibition - 0.8626 86.26%
CYP2C19 inhibition - 0.6266 62.66%
CYP2D6 inhibition - 0.7269 72.69%
CYP1A2 inhibition + 0.7736 77.36%
CYP2C8 inhibition - 0.5757 57.57%
CYP inhibitory promiscuity - 0.6546 65.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6771 67.71%
Eye corrosion - 0.9709 97.09%
Eye irritation - 0.9894 98.94%
Skin irritation - 0.6508 65.08%
Skin corrosion - 0.8303 83.03%
Ames mutagenesis + 0.8363 83.63%
Human Ether-a-go-go-Related Gene inhibition + 0.7172 71.72%
Micronuclear + 0.5700 57.00%
Hepatotoxicity + 0.6069 60.69%
skin sensitisation - 0.8724 87.24%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.8769 87.69%
Acute Oral Toxicity (c) III 0.5031 50.31%
Estrogen receptor binding + 0.8417 84.17%
Androgen receptor binding + 0.6420 64.20%
Thyroid receptor binding + 0.7078 70.78%
Glucocorticoid receptor binding - 0.5290 52.90%
Aromatase binding - 0.5816 58.16%
PPAR gamma + 0.5183 51.83%
Honey bee toxicity - 0.9451 94.51%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity - 0.7515 75.15%

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 95.19% 98.95%
CHEMBL5805 Q9NR97 Toll-like receptor 8 93.95% 96.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.59% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.83% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.33% 99.23%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 88.57% 96.67%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.11% 85.14%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.41% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.25% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.29% 89.00%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 83.63% 92.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.62% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.08% 91.11%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 82.70% 90.71%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 82.68% 96.39%
CHEMBL1951 P21397 Monoamine oxidase A 81.85% 91.49%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 81.73% 96.47%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 81.43% 96.42%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.14% 97.09%
CHEMBL2056 P21728 Dopamine D1 receptor 80.53% 91.00%

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.
Tabernaemontana elegans

Cross-Links

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PubChem 44179503
LOTUS LTS0251182
wikiData Q105283353