Tiliacorinine

Details

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Internal ID 05c6f508-6795-4a14-ba26-115a55078ada
Taxonomy Lignans, neolignans and related compounds
IUPAC Name (8S,21S)-16,27-dimethoxy-7,22-dimethyl-29,31-dioxa-7,22-diazaoctacyclo[19.9.3.14,30.110,14.115,19.03,8.025,33.028,32]hexatriaconta-1(30),2,4(34),10(36),11,13,15,17,19(35),25,27,32-dodecaen-13-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C36H36N2O5/c1-37-11-9-22-17-31-32-19-24(22)27(37)15-20-5-7-29(39)25(13-20)26-14-21(6-8-30(26)40-3)16-28-34-23(10-12-38(28)2)18-33(41-4)35(42-31)36(34)43-32/h5-8,13-14,17-19,27-28,39H,9-12,15-16H2,1-4H3/t27-,28-/m0/s1
InChI Key DQIJJKSVYLLDQW-NSOVKSMOSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C36H36N2O5
Molecular Weight 576.70 g/mol
Exact Mass 576.26242225 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 6.10
Atomic LogP (AlogP) 6.83
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tiliacorinine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8714 87.14%
Caco-2 + 0.6813 68.13%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.4491 44.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9282 92.82%
OATP1B3 inhibitior + 0.9502 95.02%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.9889 98.89%
P-glycoprotein inhibitior + 0.9539 95.39%
P-glycoprotein substrate + 0.5579 55.79%
CYP3A4 substrate + 0.6799 67.99%
CYP2C9 substrate + 0.7890 78.90%
CYP2D6 substrate + 0.7253 72.53%
CYP3A4 inhibition - 0.9342 93.42%
CYP2C9 inhibition - 0.9575 95.75%
CYP2C19 inhibition - 0.9382 93.82%
CYP2D6 inhibition - 0.9048 90.48%
CYP1A2 inhibition - 0.8931 89.31%
CYP2C8 inhibition + 0.4949 49.49%
CYP inhibitory promiscuity - 0.9726 97.26%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6538 65.38%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9495 94.95%
Skin irritation - 0.7793 77.93%
Skin corrosion - 0.9528 95.28%
Ames mutagenesis + 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8759 87.59%
Micronuclear + 0.6200 62.00%
Hepatotoxicity - 0.9250 92.50%
skin sensitisation - 0.8868 88.68%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7599 75.99%
Acute Oral Toxicity (c) III 0.7725 77.25%
Estrogen receptor binding + 0.7554 75.54%
Androgen receptor binding + 0.7675 76.75%
Thyroid receptor binding + 0.6327 63.27%
Glucocorticoid receptor binding + 0.8686 86.86%
Aromatase binding + 0.5985 59.85%
PPAR gamma + 0.5683 56.83%
Honey bee toxicity - 0.7997 79.97%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.7068 70.68%

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 99.46% 96.09%
CHEMBL217 P14416 Dopamine D2 receptor 96.02% 95.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.55% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.19% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 94.19% 91.49%
CHEMBL2581 P07339 Cathepsin D 93.87% 98.95%
CHEMBL2056 P21728 Dopamine D1 receptor 93.73% 91.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.01% 91.11%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.61% 89.62%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.55% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.25% 86.33%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.75% 93.40%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.44% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.41% 89.00%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 87.27% 90.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.09% 94.00%
CHEMBL2535 P11166 Glucose transporter 86.05% 98.75%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 85.84% 82.38%
CHEMBL4208 P20618 Proteasome component C5 85.40% 90.00%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 84.72% 95.78%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 84.50% 80.78%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 82.89% 96.38%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.87% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.68% 92.94%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 81.17% 96.86%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 80.49% 95.53%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 80.05% 82.67%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.03% 99.15%

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.
Tiliacora acuminata
Tiliacora triandra

Cross-Links

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PubChem 442369
NPASS NPC65312
ChEMBL CHEMBL2017489
LOTUS LTS0100997
wikiData Q27108444