Goniothalesacetate

Details

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Internal ID 4d3fae57-4aeb-4056-a385-69c88e98a4b0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name methyl (3R)-3-[(2S,3S,4R,5R)-3-acetyloxy-4-hydroxy-5-phenyloxolan-2-yl]-3-methoxypropanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H22O7/c1-10(18)23-17-14(20)15(11-7-5-4-6-8-11)24-16(17)12(21-2)9-13(19)22-3/h4-8,12,14-17,20H,9H2,1-3H3/t12-,14-,15-,16+,17+/m1/s1
InChI Key LHWIBJDDRHTINZ-MNLARUNXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O7
Molecular Weight 338.40 g/mol
Exact Mass 338.13655304 g/mol
Topological Polar Surface Area (TPSA) 91.30 Ų
XlogP 0.50
Atomic LogP (AlogP) 1.00
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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methyl (3R)-3-[(2S,3S,4R,5R)-3-acetyloxy-4-hydroxy-5-phenyloxolan-2-yl]-3-methoxypropanoate

2D Structure

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2D Structure of Goniothalesacetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9585 95.85%
Caco-2 + 0.6949 69.49%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.8054 80.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8713 87.13%
OATP1B3 inhibitior + 0.8098 80.98%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7190 71.90%
P-glycoprotein inhibitior - 0.5872 58.72%
P-glycoprotein substrate - 0.7819 78.19%
CYP3A4 substrate + 0.5340 53.40%
CYP2C9 substrate - 0.7891 78.91%
CYP2D6 substrate - 0.8228 82.28%
CYP3A4 inhibition - 0.9347 93.47%
CYP2C9 inhibition - 0.9334 93.34%
CYP2C19 inhibition - 0.8768 87.68%
CYP2D6 inhibition - 0.9297 92.97%
CYP1A2 inhibition - 0.8714 87.14%
CYP2C8 inhibition - 0.7660 76.60%
CYP inhibitory promiscuity - 0.8566 85.66%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8911 89.11%
Carcinogenicity (trinary) Non-required 0.5702 57.02%
Eye corrosion - 0.9656 96.56%
Eye irritation - 0.9168 91.68%
Skin irritation - 0.8253 82.53%
Skin corrosion - 0.9764 97.64%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4284 42.84%
Micronuclear - 0.5882 58.82%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8953 89.53%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.7906 79.06%
Acute Oral Toxicity (c) III 0.5897 58.97%
Estrogen receptor binding - 0.5837 58.37%
Androgen receptor binding - 0.5653 56.53%
Thyroid receptor binding - 0.5521 55.21%
Glucocorticoid receptor binding - 0.7227 72.27%
Aromatase binding - 0.8755 87.55%
PPAR gamma - 0.6952 69.52%
Honey bee toxicity - 0.8150 81.50%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.8235 82.35%

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 97.94% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.52% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.00% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 93.56% 83.82%
CHEMBL3401 O75469 Pregnane X receptor 93.35% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.67% 95.56%
CHEMBL5028 O14672 ADAM10 86.03% 97.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.96% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.89% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.30% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.95% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.13% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.09% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.06% 97.21%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 80.50% 94.08%
CHEMBL221 P23219 Cyclooxygenase-1 80.07% 90.17%

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.
Goniothalamus amuyon
Gymnacranthera farquhariana var. paniculata
Lysimachia monelli
Ornithogalum thyrsoides

Cross-Links

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PubChem 16079979
NPASS NPC201591
LOTUS LTS0104506
wikiData Q105152013