dihydrophaseic acid 4-O-beta-D-glucoside

Details

Top
Internal ID 792b5380-6d2b-445a-98de-b48f257e303d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Abscisic acids and derivatives
IUPAC Name (2Z,4E)-5-[(1R,3S,5R,8S)-8-hydroxy-1,5-dimethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoic acid
SMILES (Canonical) CC(=CC(=O)O)C=CC1(C2(CC(CC1(OC2)C)OC3C(C(C(C(O3)CO)O)O)O)C)O
SMILES (Isomeric) C/C(=C/C(=O)O)/C=C/[C@@]1([C@@]2(C[C@@H](C[C@]1(OC2)C)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)C)O
InChI InChI=1S/C21H32O10/c1-11(6-14(23)24)4-5-21(28)19(2)7-12(8-20(21,3)29-10-19)30-18-17(27)16(26)15(25)13(9-22)31-18/h4-6,12-13,15-18,22,25-28H,7-10H2,1-3H3,(H,23,24)/b5-4+,11-6-/t12-,13+,15+,16-,17+,18+,19+,20+,21-/m0/s1
InChI Key UHHVHDDICOEBTQ-WTZDRGJSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C21H32O10
Molecular Weight 444.50 g/mol
Exact Mass 444.19954721 g/mol
Topological Polar Surface Area (TPSA) 166.00 Ų
XlogP -0.70
Atomic LogP (AlogP) -0.92
H-Bond Acceptor 9
H-Bond Donor 6
Rotatable Bonds 6

Synonyms

Top
(2Z,4E)-5-[(1R,3S,5R,8S)-3-(beta-D-glucopyranosyloxy)-8-hydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]oct-8-yl]-3-methylpenta-2,4-dienoic acid
CHEBI:23758
Dihydrophaseic acid 4'-O-beta-D-glucopyranoside
AKOS040734351
dihydrophaseic acid-4-O-beta-glucoside
Dihydrophaseic acid-4'-O-beta-D-glucopyranoside
Q27109813
(2Z,4E)-5-[(1R,3S,5R,8S)-8-hydroxy-1,5-dimethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoic acid

2D Structure

Top
2D Structure of dihydrophaseic acid 4-O-beta-D-glucoside

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5926 59.26%
Caco-2 - 0.7964 79.64%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.8714 87.14%
Subcellular localzation Mitochondria 0.7367 73.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8886 88.86%
OATP1B3 inhibitior + 0.9211 92.11%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8407 84.07%
P-glycoprotein inhibitior - 0.7133 71.33%
P-glycoprotein substrate - 0.8194 81.94%
CYP3A4 substrate + 0.6375 63.75%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8886 88.86%
CYP3A4 inhibition - 0.9364 93.64%
CYP2C9 inhibition - 0.8819 88.19%
CYP2C19 inhibition - 0.8705 87.05%
CYP2D6 inhibition - 0.9420 94.20%
CYP1A2 inhibition - 0.8916 89.16%
CYP2C8 inhibition - 0.7326 73.26%
CYP inhibitory promiscuity - 0.9036 90.36%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6523 65.23%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.9488 94.88%
Skin irritation - 0.6656 66.56%
Skin corrosion - 0.9493 94.93%
Ames mutagenesis - 0.6570 65.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6165 61.65%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.6858 68.58%
skin sensitisation - 0.8862 88.62%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.6017 60.17%
Acute Oral Toxicity (c) I 0.4798 47.98%
Estrogen receptor binding + 0.7414 74.14%
Androgen receptor binding + 0.6825 68.25%
Thyroid receptor binding + 0.6767 67.67%
Glucocorticoid receptor binding + 0.6612 66.12%
Aromatase binding + 0.7327 73.27%
PPAR gamma + 0.6027 60.27%
Honey bee toxicity - 0.6991 69.91%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6855 68.55%
Fish aquatic toxicity + 0.9687 96.87%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.85% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.25% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.49% 94.45%
CHEMBL2061 P19793 Retinoid X receptor alpha 92.59% 91.67%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.23% 97.09%
CHEMBL1870 P28702 Retinoid X receptor beta 86.21% 95.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.09% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.94% 89.00%
CHEMBL2004 P48443 Retinoid X receptor gamma 84.04% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 83.77% 92.50%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 82.93% 91.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.48% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 82.38% 91.19%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.32% 95.50%
CHEMBL2072 P35499 Sodium channel protein type IV alpha subunit 81.88% 92.32%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.52% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.22% 99.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.95% 94.33%

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.
Artemisia anomala
Juniperus phoenicea
Persea americana

Cross-Links

Top
PubChem 11988281
NPASS NPC19837
LOTUS LTS0151763
wikiData Q27109813