Talathermophilin B

Details

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Internal ID 9002bbc5-362c-4e70-ab1a-016da8e5d877
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name (6S)-3-[[7,7-dimethyl-2-(2-methylbut-3-en-2-yl)-1H-pyrano[2,3-g]indol-3-yl]methylidene]-6-methylpiperazine-2,5-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H27N3O3/c1-7-23(3,4)20-16(12-17-22(29)25-13(2)21(28)26-17)14-8-9-18-15(19(14)27-20)10-11-24(5,6)30-18/h7-13,27H,1H2,2-6H3,(H,25,29)(H,26,28)/t13-/m0/s1
InChI Key WTWFASVQVSRLOB-ZDUSSCGKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H27N3O3
Molecular Weight 405.50 g/mol
Exact Mass 405.20524173 g/mol
Topological Polar Surface Area (TPSA) 83.20 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.79
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Talathermophilin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9900 99.00%
Caco-2 - 0.6317 63.17%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7306 73.06%
OATP2B1 inhibitior - 0.8529 85.29%
OATP1B1 inhibitior + 0.8607 86.07%
OATP1B3 inhibitior + 0.9445 94.45%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9364 93.64%
P-glycoprotein inhibitior + 0.6813 68.13%
P-glycoprotein substrate + 0.5888 58.88%
CYP3A4 substrate + 0.6591 65.91%
CYP2C9 substrate - 0.6171 61.71%
CYP2D6 substrate - 0.8608 86.08%
CYP3A4 inhibition + 0.5524 55.24%
CYP2C9 inhibition + 0.7186 71.86%
CYP2C19 inhibition + 0.6061 60.61%
CYP2D6 inhibition - 0.8411 84.11%
CYP1A2 inhibition + 0.6949 69.49%
CYP2C8 inhibition + 0.5750 57.50%
CYP inhibitory promiscuity + 0.8735 87.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5263 52.63%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.9650 96.50%
Skin irritation - 0.8230 82.30%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3831 38.31%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8484 84.84%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.4569 45.69%
Acute Oral Toxicity (c) III 0.5945 59.45%
Estrogen receptor binding + 0.8541 85.41%
Androgen receptor binding + 0.7352 73.52%
Thyroid receptor binding + 0.7695 76.95%
Glucocorticoid receptor binding + 0.7640 76.40%
Aromatase binding + 0.6635 66.35%
PPAR gamma + 0.8422 84.22%
Honey bee toxicity - 0.7115 71.15%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9609 96.09%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.70% 97.25%
CHEMBL2581 P07339 Cathepsin D 96.48% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.24% 91.11%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 95.84% 92.88%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 94.43% 94.80%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.70% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 93.47% 91.49%
CHEMBL1937 Q92769 Histone deacetylase 2 92.40% 94.75%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 91.81% 93.40%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.66% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.26% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.27% 99.23%
CHEMBL3310 Q96DB2 Histone deacetylase 11 88.08% 88.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.26% 96.77%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.63% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.60% 96.09%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 83.71% 81.14%
CHEMBL5103 Q969S8 Histone deacetylase 10 83.59% 90.08%
CHEMBL1907 P15144 Aminopeptidase N 82.68% 93.31%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 82.18% 80.96%
CHEMBL3401 O75469 Pregnane X receptor 81.73% 94.73%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.49% 100.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.62% 95.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.57% 93.56%
CHEMBL2179 P04062 Beta-glucocerebrosidase 80.14% 85.31%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139587864
LOTUS LTS0262760
wikiData Q105312833