Terrusnolide C

Details

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Internal ID 4dd7b0be-28e2-4470-82fe-94f026154197
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]-2-methoxy-4-(4-methoxyphenyl)-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H26O6/c1-24(2)20(25)13-16-11-14(5-10-19(16)30-24)12-18-21(22(26)29-23(18)28-4)15-6-8-17(27-3)9-7-15/h5-11,20,23,25H,12-13H2,1-4H3/t20?,23-/m1/s1
InChI Key BHQRPPBXAQQFON-GWQXNCQPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H26O6
Molecular Weight 410.50 g/mol
Exact Mass 410.17293854 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.30
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Terrusnolide C

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 + 0.5348 53.48%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7539 75.39%
OATP2B1 inhibitior - 0.8632 86.32%
OATP1B1 inhibitior + 0.8633 86.33%
OATP1B3 inhibitior - 0.3223 32.23%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9682 96.82%
P-glycoprotein inhibitior + 0.7758 77.58%
P-glycoprotein substrate - 0.6800 68.00%
CYP3A4 substrate + 0.6704 67.04%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.8311 83.11%
CYP3A4 inhibition + 0.5803 58.03%
CYP2C9 inhibition - 0.6343 63.43%
CYP2C19 inhibition + 0.5555 55.55%
CYP2D6 inhibition - 0.8632 86.32%
CYP1A2 inhibition - 0.8184 81.84%
CYP2C8 inhibition + 0.5785 57.85%
CYP inhibitory promiscuity - 0.5108 51.08%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4369 43.69%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.9054 90.54%
Skin irritation - 0.7403 74.03%
Skin corrosion - 0.9465 94.65%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5410 54.10%
Micronuclear - 0.5700 57.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.7690 76.90%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5702 57.02%
Acute Oral Toxicity (c) I 0.4164 41.64%
Estrogen receptor binding + 0.8923 89.23%
Androgen receptor binding + 0.8027 80.27%
Thyroid receptor binding + 0.7085 70.85%
Glucocorticoid receptor binding + 0.8307 83.07%
Aromatase binding + 0.5604 56.04%
PPAR gamma + 0.7773 77.73%
Honey bee toxicity - 0.7131 71.31%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9894 98.94%

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 98.51% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.90% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.41% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 96.32% 90.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.59% 93.99%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.44% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.94% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.77% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.70% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.64% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.29% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 91.22% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.30% 97.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 89.77% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.39% 92.62%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 88.12% 95.53%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.36% 99.17%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.22% 97.14%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.43% 96.95%
CHEMBL1944 P08473 Neprilysin 84.14% 92.63%
CHEMBL4208 P20618 Proteasome component C5 83.91% 90.00%
CHEMBL5555 O00767 Acyl-CoA desaturase 83.46% 97.50%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.16% 95.71%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.61% 96.77%
CHEMBL1907 P15144 Aminopeptidase N 81.04% 93.31%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.58% 91.07%
CHEMBL4040 P28482 MAP kinase ERK2 80.30% 83.82%

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 146684409
LOTUS LTS0064368
wikiData Q104935873