(5S,6R,7S,8S)-Goniotriol

Details

Top
Internal ID 125a7942-a005-4ead-aaba-16ce3f48d397
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives > Dihydropyranones
IUPAC Name (2R,3S)-2-[(1S,2S)-1,2-dihydroxy-2-phenylethyl]-3-hydroxy-2,3-dihydropyran-6-one
SMILES (Canonical) C1=CC=C(C=C1)C(C(C2C(C=CC(=O)O2)O)O)O
SMILES (Isomeric) C1=CC=C(C=C1)[C@@H]([C@@H]([C@H]2[C@H](C=CC(=O)O2)O)O)O
InChI InChI=1S/C13H14O5/c14-9-6-7-10(15)18-13(9)12(17)11(16)8-4-2-1-3-5-8/h1-7,9,11-14,16-17H/t9-,11-,12-,13+/m0/s1
InChI Key AWCDBKHWVKLXEE-XYJRDEOASA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C13H14O5
Molecular Weight 250.25 g/mol
Exact Mass 250.08412354 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 0.40
Atomic LogP (AlogP) -0.08
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (5S,6R,7S,8S)-Goniotriol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6423 64.23%
Caco-2 - 0.7970 79.70%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5651 56.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9338 93.38%
OATP1B3 inhibitior + 0.9660 96.60%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9191 91.91%
P-glycoprotein inhibitior - 0.9095 90.95%
P-glycoprotein substrate - 0.9362 93.62%
CYP3A4 substrate - 0.5855 58.55%
CYP2C9 substrate - 0.6314 63.14%
CYP2D6 substrate - 0.8707 87.07%
CYP3A4 inhibition - 0.5739 57.39%
CYP2C9 inhibition - 0.9099 90.99%
CYP2C19 inhibition - 0.9553 95.53%
CYP2D6 inhibition - 0.9645 96.45%
CYP1A2 inhibition - 0.9020 90.20%
CYP2C8 inhibition - 0.9719 97.19%
CYP inhibitory promiscuity - 0.7402 74.02%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6305 63.05%
Eye corrosion - 0.9805 98.05%
Eye irritation + 0.5800 58.00%
Skin irritation + 0.5466 54.66%
Skin corrosion - 0.9329 93.29%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8968 89.68%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.5908 59.08%
skin sensitisation - 0.6283 62.83%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.7364 73.64%
Acute Oral Toxicity (c) IV 0.4995 49.95%
Estrogen receptor binding - 0.6464 64.64%
Androgen receptor binding - 0.7903 79.03%
Thyroid receptor binding - 0.6851 68.51%
Glucocorticoid receptor binding - 0.6402 64.02%
Aromatase binding - 0.7185 71.85%
PPAR gamma - 0.6108 61.08%
Honey bee toxicity - 0.9024 90.24%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.8607 86.07%

Targets

Top

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.52% 85.14%
CHEMBL2581 P07339 Cathepsin D 94.86% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.30% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.05% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 84.70% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.60% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.34% 89.00%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 82.20% 87.67%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.19% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.11% 86.33%

Plants that contains it

Top
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

Top
PubChem 26496963
NPASS NPC91815