Truncateol V

Details

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Internal ID 75a91a67-6e27-4c7f-a005-cbe1fe88e915
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name (2R)-2-(2-hydroxypropan-2-yl)-6,6-dimethyl-3,7-dihydro-2H-furo[2,3-g]chromen-8-one
SMILES (Canonical) CC1(CC(=O)C2=C(O1)C=C3CC(OC3=C2)C(C)(C)O)C
SMILES (Isomeric) CC1(CC(=O)C2=C(O1)C=C3C[C@@H](OC3=C2)C(C)(C)O)C
InChI InChI=1S/C16H20O4/c1-15(2)8-11(17)10-7-12-9(5-13(10)20-15)6-14(19-12)16(3,4)18/h5,7,14,18H,6,8H2,1-4H3/t14-/m1/s1
InChI Key CGEURPDLOCVPML-CQSZACIVSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20O4
Molecular Weight 276.33 g/mol
Exact Mass 276.13615911 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.50
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL465528

2D Structure

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2D Structure of Truncateol V

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.6793 67.93%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7643 76.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9023 90.23%
OATP1B3 inhibitior + 0.9318 93.18%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8689 86.89%
P-glycoprotein inhibitior - 0.8931 89.31%
P-glycoprotein substrate - 0.8680 86.80%
CYP3A4 substrate + 0.5586 55.86%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7153 71.53%
CYP3A4 inhibition - 0.8127 81.27%
CYP2C9 inhibition - 0.7971 79.71%
CYP2C19 inhibition - 0.7029 70.29%
CYP2D6 inhibition - 0.8188 81.88%
CYP1A2 inhibition + 0.6172 61.72%
CYP2C8 inhibition - 0.8688 86.88%
CYP inhibitory promiscuity - 0.8742 87.42%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5260 52.60%
Eye corrosion - 0.9851 98.51%
Eye irritation - 0.5215 52.15%
Skin irritation - 0.7034 70.34%
Skin corrosion - 0.9089 90.89%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7261 72.61%
Micronuclear - 0.6241 62.41%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.7019 70.19%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.5757 57.57%
Acute Oral Toxicity (c) III 0.6527 65.27%
Estrogen receptor binding - 0.6049 60.49%
Androgen receptor binding - 0.7263 72.63%
Thyroid receptor binding - 0.5342 53.42%
Glucocorticoid receptor binding - 0.5210 52.10%
Aromatase binding - 0.6025 60.25%
PPAR gamma + 0.6311 63.11%
Honey bee toxicity - 0.8360 83.60%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9031 90.31%

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 97.81% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.82% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.36% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.67% 95.56%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 89.50% 93.04%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 88.19% 89.34%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.70% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.46% 96.77%
CHEMBL2850 P49840 Glycogen synthase kinase-3 alpha 86.64% 88.84%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.70% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.34% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.02% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.51% 95.89%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 83.40% 98.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.27% 95.71%
CHEMBL3401 O75469 Pregnane X receptor 82.66% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.58% 100.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.31% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.10% 94.45%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 81.68% 85.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.55% 99.23%

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 44567581
LOTUS LTS0109006
wikiData Q104957572