Terrusnolide B

Details

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Internal ID a3053b99-1672-42bf-8d81-73de5c25a7c3
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name (2R)-3-[(3-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)methyl]-4-(4-hydroxyphenyl)-2-methoxy-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H24O6/c1-23(2)19(25)12-15-10-13(4-9-18(15)29-23)11-17-20(21(26)28-22(17)27-3)14-5-7-16(24)8-6-14/h4-10,19,22,24-25H,11-12H2,1-3H3/t19?,22-/m1/s1
InChI Key OOGJVXKOBYYOLN-AVKWCDSFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H24O6
Molecular Weight 396.40 g/mol
Exact Mass 396.15728848 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.99
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Terrusnolide B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 - 0.5381 53.81%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7557 75.57%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.8026 80.26%
OATP1B3 inhibitior - 0.2894 28.94%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9209 92.09%
P-glycoprotein inhibitior + 0.6335 63.35%
P-glycoprotein substrate - 0.5814 58.14%
CYP3A4 substrate + 0.6692 66.92%
CYP2C9 substrate - 0.8015 80.15%
CYP2D6 substrate - 0.8285 82.85%
CYP3A4 inhibition - 0.5436 54.36%
CYP2C9 inhibition - 0.5988 59.88%
CYP2C19 inhibition + 0.5068 50.68%
CYP2D6 inhibition - 0.8427 84.27%
CYP1A2 inhibition - 0.8110 81.10%
CYP2C8 inhibition + 0.7628 76.28%
CYP inhibitory promiscuity + 0.5413 54.13%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.4361 43.61%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.8598 85.98%
Skin irritation - 0.7455 74.55%
Skin corrosion - 0.9444 94.44%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7660 76.60%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.5073 50.73%
skin sensitisation - 0.7783 77.83%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.7127 71.27%
Acute Oral Toxicity (c) I 0.4791 47.91%
Estrogen receptor binding + 0.8708 87.08%
Androgen receptor binding + 0.8324 83.24%
Thyroid receptor binding + 0.6639 66.39%
Glucocorticoid receptor binding + 0.8650 86.50%
Aromatase binding + 0.6242 62.42%
PPAR gamma + 0.7657 76.57%
Honey bee toxicity - 0.6433 64.33%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9898 98.98%

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
CHEMBL2581 P07339 Cathepsin D 98.62% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.95% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.81% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.50% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.43% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.24% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.90% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.53% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 91.40% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.15% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 89.57% 83.82%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.44% 93.99%
CHEMBL233 P35372 Mu opioid receptor 88.27% 97.93%
CHEMBL4630 O14757 Serine/threonine-protein kinase Chk1 87.73% 97.03%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.72% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.46% 97.09%
CHEMBL5555 O00767 Acyl-CoA desaturase 87.15% 97.50%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 86.50% 95.53%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.43% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.07% 96.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.09% 97.14%
CHEMBL3922 P50579 Methionine aminopeptidase 2 83.57% 97.28%
CHEMBL1937 Q92769 Histone deacetylase 2 83.05% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.03% 89.00%
CHEMBL242 Q92731 Estrogen receptor beta 82.43% 98.35%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.05% 91.71%
CHEMBL3401 O75469 Pregnane X receptor 81.88% 94.73%
CHEMBL1944 P08473 Neprilysin 80.97% 92.63%

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 146684408
LOTUS LTS0169796
wikiData Q105195369