Tabertinggine

Details

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Internal ID 6f945f11-885e-4a34-b268-6ce16d2210e6
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Beta carbolines
IUPAC Name 1-[(1R,15R)-3,13-diazapentacyclo[13.3.1.01,13.02,10.04,9]nonadeca-2(10),4,6,8,17-pentaen-17-yl]ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H20N2O/c1-12(22)14-8-13-9-19(10-14)18-16(6-7-21(19)11-13)15-4-2-3-5-17(15)20-18/h2-5,10,13,20H,6-9,11H2,1H3/t13-,19-/m1/s1
InChI Key RIZDDRXJJMJQIS-BFUOFWGJSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H20N2O
Molecular Weight 292.40 g/mol
Exact Mass 292.157563266 g/mol
Topological Polar Surface Area (TPSA) 36.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tabertinggine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 + 0.8847 88.47%
Blood Brain Barrier + 0.9629 96.29%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5088 50.88%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9284 92.84%
OATP1B3 inhibitior + 0.9441 94.41%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior + 0.6750 67.50%
BSEP inhibitior + 0.6787 67.87%
P-glycoprotein inhibitior - 0.7143 71.43%
P-glycoprotein substrate + 0.5234 52.34%
CYP3A4 substrate + 0.6518 65.18%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.6604 66.04%
CYP3A4 inhibition + 0.5495 54.95%
CYP2C9 inhibition - 0.7093 70.93%
CYP2C19 inhibition - 0.8145 81.45%
CYP2D6 inhibition + 0.7567 75.67%
CYP1A2 inhibition - 0.6123 61.23%
CYP2C8 inhibition - 0.7817 78.17%
CYP inhibitory promiscuity + 0.6813 68.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.7509 75.09%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.9775 97.75%
Skin irritation - 0.7193 71.93%
Skin corrosion - 0.9264 92.64%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8782 87.82%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8311 83.11%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.6959 69.59%
Acute Oral Toxicity (c) III 0.5603 56.03%
Estrogen receptor binding + 0.6807 68.07%
Androgen receptor binding + 0.6458 64.58%
Thyroid receptor binding - 0.6039 60.39%
Glucocorticoid receptor binding - 0.6474 64.74%
Aromatase binding - 0.5801 58.01%
PPAR gamma - 0.5701 57.01%
Honey bee toxicity - 0.9123 91.23%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9037 90.37%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.51% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.52% 85.14%
CHEMBL2581 P07339 Cathepsin D 95.51% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.67% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.15% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.47% 99.23%
CHEMBL3310 Q96DB2 Histone deacetylase 11 90.24% 88.56%
CHEMBL2535 P11166 Glucose transporter 88.85% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.29% 94.45%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.64% 94.62%
CHEMBL255 P29275 Adenosine A2b receptor 86.32% 98.59%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 85.83% 96.39%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.12% 89.00%
CHEMBL217 P14416 Dopamine D2 receptor 83.94% 95.62%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 83.66% 97.50%
CHEMBL4073 P09237 Matrix metalloproteinase 7 82.44% 97.56%
CHEMBL5028 O14672 ADAM10 81.96% 97.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.10% 97.09%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 80.05% 94.08%

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 bovina

Cross-Links

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PubChem 102103442
LOTUS LTS0176062
wikiData Q105237303