(+)-Goniothalesdiol

Details

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Internal ID 9f2ad693-b364-4437-9838-9b7102c2c902
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name methyl 3-[(2S,3S,4S,5R)-3,4-dihydroxy-5-phenyloxolan-2-yl]propanoate
SMILES (Canonical) COC(=O)CCC1C(C(C(O1)C2=CC=CC=C2)O)O
SMILES (Isomeric) COC(=O)CC[C@H]1[C@H]([C@@H]([C@H](O1)C2=CC=CC=C2)O)O
InChI InChI=1S/C14H18O5/c1-18-11(15)8-7-10-12(16)13(17)14(19-10)9-5-3-2-4-6-9/h2-6,10,12-14,16-17H,7-8H2,1H3/t10-,12+,13-,14+/m0/s1
InChI Key RUDVTXZKYPJLFH-AHLTXXRQSA-N
Popularity 11 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O5
Molecular Weight 266.29 g/mol
Exact Mass 266.11542367 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.80
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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204975-45-1
methyl 3-[(2S,3S,4S,5R)-3,4-dihydroxy-5-phenyloxolan-2-yl]propanoate
4,7-ANHYDRO-2,3-DIDEOXY-7R-C-PHENYL-D-XYLO-HEPTONIC ACID, METHYL ESTER
Goniothalesdiol
SCHEMBL6078985
CHEBI:188220
AKOS040754614
Methyl 3-((2S,3S,4S,5R)-3,4-dihydroxy-5-phenyltetrahydrofuran-2-yl)propanoate

2D Structure

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2D Structure of (+)-Goniothalesdiol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8278 82.78%
Caco-2 + 0.5733 57.33%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8300 83.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8512 85.12%
OATP1B3 inhibitior + 0.9244 92.44%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9159 91.59%
P-glycoprotein inhibitior - 0.9226 92.26%
P-glycoprotein substrate - 0.9449 94.49%
CYP3A4 substrate - 0.5575 55.75%
CYP2C9 substrate - 0.8047 80.47%
CYP2D6 substrate - 0.8075 80.75%
CYP3A4 inhibition - 0.8991 89.91%
CYP2C9 inhibition - 0.7127 71.27%
CYP2C19 inhibition - 0.6490 64.90%
CYP2D6 inhibition - 0.9368 93.68%
CYP1A2 inhibition - 0.7240 72.40%
CYP2C8 inhibition - 0.6499 64.99%
CYP inhibitory promiscuity - 0.7700 77.00%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5992 59.92%
Eye corrosion - 0.9826 98.26%
Eye irritation - 0.9470 94.70%
Skin irritation - 0.6657 66.57%
Skin corrosion - 0.8925 89.25%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4326 43.26%
Micronuclear - 0.7541 75.41%
Hepatotoxicity + 0.5116 51.16%
skin sensitisation - 0.8980 89.80%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.5559 55.59%
Acute Oral Toxicity (c) III 0.5464 54.64%
Estrogen receptor binding - 0.7037 70.37%
Androgen receptor binding - 0.6871 68.71%
Thyroid receptor binding - 0.8087 80.87%
Glucocorticoid receptor binding - 0.8158 81.58%
Aromatase binding - 0.8966 89.66%
PPAR gamma - 0.6083 60.83%
Honey bee toxicity - 0.9595 95.95%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.7330 73.30%

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
CHEMBL4040 P28482 MAP kinase ERK2 98.83% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.53% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.37% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 94.66% 90.17%
CHEMBL2581 P07339 Cathepsin D 91.34% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.20% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.56% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.25% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.63% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.03% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.78% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.67% 86.33%
CHEMBL5028 O14672 ADAM10 82.25% 97.50%

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 borneensis

Cross-Links

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PubChem 10061436
LOTUS LTS0101188
wikiData Q105245575