Thaliglucinone

Details

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Internal ID 8813278c-e564-4916-a6c2-723d247d6b4d
Taxonomy Alkaloids and derivatives > 6,6a-secoaporphines
IUPAC Name 12-[2-(dimethylamino)ethyl]-14-methoxy-3,5,16-trioxapentacyclo[9.6.2.02,6.08,18.015,19]nonadeca-1(18),2(6),7,9,11(19),12,14-heptaen-17-one
SMILES (Canonical) CN(C)CCC1=CC(=C2C3=C1C=CC4=CC5=C(C(=C43)C(=O)O2)OCO5)OC
SMILES (Isomeric) CN(C)CCC1=CC(=C2C3=C1C=CC4=CC5=C(C(=C43)C(=O)O2)OCO5)OC
InChI InChI=1S/C21H19NO5/c1-22(2)7-6-11-8-14(24-3)20-17-13(11)5-4-12-9-15-19(26-10-25-15)18(16(12)17)21(23)27-20/h4-5,8-9H,6-7,10H2,1-3H3
InChI Key ZLVXQJKCDNGHDK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H19NO5
Molecular Weight 365.40 g/mol
Exact Mass 365.12632271 g/mol
Topological Polar Surface Area (TPSA) 57.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.38
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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35988-96-6
DTXSID60189547

2D Structure

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2D Structure of Thaliglucinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9407 94.07%
Caco-2 + 0.8243 82.43%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.4371 43.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9092 90.92%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.6584 65.84%
P-glycoprotein inhibitior + 0.7212 72.12%
P-glycoprotein substrate - 0.5544 55.44%
CYP3A4 substrate + 0.6473 64.73%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.6917 69.17%
CYP3A4 inhibition - 0.6264 62.64%
CYP2C9 inhibition - 0.5393 53.93%
CYP2C19 inhibition - 0.6942 69.42%
CYP2D6 inhibition + 0.6489 64.89%
CYP1A2 inhibition - 0.5808 58.08%
CYP2C8 inhibition - 0.6675 66.75%
CYP inhibitory promiscuity - 0.5362 53.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5685 56.85%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.9307 93.07%
Skin irritation - 0.7954 79.54%
Skin corrosion - 0.9359 93.59%
Ames mutagenesis + 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7792 77.92%
Micronuclear - 0.5726 57.26%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8240 82.40%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.8532 85.32%
Acute Oral Toxicity (c) III 0.6990 69.90%
Estrogen receptor binding + 0.7748 77.48%
Androgen receptor binding + 0.6958 69.58%
Thyroid receptor binding + 0.6343 63.43%
Glucocorticoid receptor binding + 0.8284 82.84%
Aromatase binding + 0.7667 76.67%
PPAR gamma + 0.7269 72.69%
Honey bee toxicity - 0.7175 71.75%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8300 83.00%

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 97.69% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.15% 96.77%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.51% 94.00%
CHEMBL2581 P07339 Cathepsin D 93.79% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.80% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.66% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 92.33% 92.62%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 92.01% 85.30%
CHEMBL240 Q12809 HERG 91.98% 89.76%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.62% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.41% 86.33%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 91.24% 96.67%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.00% 96.00%
CHEMBL2535 P11166 Glucose transporter 86.52% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.82% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.20% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 81.49% 94.73%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 81.37% 92.38%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.86% 89.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.34% 99.17%

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.
Coleonema pulchellum
Tamarix chinensis
Thalictrum flavum
Thalictrum foliolosum
Thalictrum lucidum
Thalictrum minus
Thalictrum podocarpum
Thalictrum podocarpum
Thalictrum revolutum
Thalictrum speciosissimum

Cross-Links

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PubChem 182266
NPASS NPC153319
LOTUS LTS0097837
wikiData Q83061677