Tribulusterine

Details

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Internal ID 907b5bdb-4802-449f-a118-7e1fe636ed00
Taxonomy Alkaloids and derivatives > Harmala alkaloids
IUPAC Name [2-(9H-pyrido[3,4-b]indol-1-yl)furan-3-yl]methanol
SMILES (Canonical) C1=CC=C2C(=C1)C3=C(N2)C(=NC=C3)C4=C(C=CO4)CO
SMILES (Isomeric) C1=CC=C2C(=C1)C3=C(N2)C(=NC=C3)C4=C(C=CO4)CO
InChI InChI=1S/C16H12N2O2/c19-9-10-6-8-20-16(10)15-14-12(5-7-17-15)11-3-1-2-4-13(11)18-14/h1-8,18-19H,9H2
InChI Key YFNWKBJECXFSDK-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12N2O2
Molecular Weight 264.28 g/mol
Exact Mass 264.089877630 g/mol
Topological Polar Surface Area (TPSA) 62.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 3.47
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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Tribulusterine
SCHEMBL20622611
BDBM50458320

2D Structure

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2D Structure of Tribulusterine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9931 99.31%
Caco-2 - 0.7883 78.83%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7197 71.97%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.9275 92.75%
OATP1B3 inhibitior + 0.9410 94.10%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6856 68.56%
P-glycoprotein inhibitior - 0.7956 79.56%
P-glycoprotein substrate - 0.8366 83.66%
CYP3A4 substrate - 0.5108 51.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7952 79.52%
CYP3A4 inhibition - 0.7048 70.48%
CYP2C9 inhibition - 0.6461 64.61%
CYP2C19 inhibition + 0.6568 65.68%
CYP2D6 inhibition - 0.6609 66.09%
CYP1A2 inhibition + 0.8184 81.84%
CYP2C8 inhibition + 0.6872 68.72%
CYP inhibitory promiscuity + 0.7950 79.50%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.7239 72.39%
Eye corrosion - 0.9931 99.31%
Eye irritation - 0.7679 76.79%
Skin irritation - 0.7888 78.88%
Skin corrosion - 0.9500 95.00%
Ames mutagenesis + 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6226 62.26%
Micronuclear + 0.8000 80.00%
Hepatotoxicity + 0.5074 50.74%
skin sensitisation - 0.8839 88.39%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.8306 83.06%
Acute Oral Toxicity (c) III 0.5689 56.89%
Estrogen receptor binding + 0.9044 90.44%
Androgen receptor binding + 0.8583 85.83%
Thyroid receptor binding + 0.6825 68.25%
Glucocorticoid receptor binding + 0.8784 87.84%
Aromatase binding + 0.9254 92.54%
PPAR gamma + 0.9011 90.11%
Honey bee toxicity - 0.9395 93.95%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity - 0.8293 82.93%

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 98.16% 91.11%
CHEMBL240 Q12809 HERG 96.06% 89.76%
CHEMBL255 P29275 Adenosine A2b receptor 93.73% 98.59%
CHEMBL3310 Q96DB2 Histone deacetylase 11 93.06% 88.56%
CHEMBL1951 P21397 Monoamine oxidase A 92.05% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.39% 89.00%
CHEMBL1781 P11387 DNA topoisomerase I 90.30% 97.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.15% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.52% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.36% 94.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.60% 91.71%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 84.42% 93.10%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 81.55% 89.44%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.25% 92.62%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.99% 94.62%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.65% 96.67%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.44% 99.23%
CHEMBL2885 P07451 Carbonic anhydrase III 80.13% 87.45%
CHEMBL1829 O15379 Histone deacetylase 3 80.05% 95.00%

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.
Crocus sativus
Tribulus terrestris

Cross-Links

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PubChem 4867627
NPASS NPC294830
LOTUS LTS0253722
wikiData Q105347710