bitalin A-12-O-beta-D-glucopyranoside

Details

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Internal ID 286727d7-0333-40a8-927f-77cad3290665
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name 1-[(2S)-2-[3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-1-en-2-yl]-2,3-dihydro-1-benzofuran-5-yl]ethanone
SMILES (Canonical) CC(=O)C1=CC2=C(C=C1)OC(C2)C(=C)COC3C(C(C(C(O3)CO)O)O)O
SMILES (Isomeric) CC(=O)C1=CC2=C(C=C1)O[C@@H](C2)C(=C)CO[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O
InChI InChI=1S/C19H24O8/c1-9(8-25-19-18(24)17(23)16(22)15(7-20)27-19)14-6-12-5-11(10(2)21)3-4-13(12)26-14/h3-5,14-20,22-24H,1,6-8H2,2H3/t14-,15+,16+,17-,18+,19+/m0/s1
InChI Key TTWVIHLNMJFBMC-SWAOIJHYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H24O8
Molecular Weight 380.40 g/mol
Exact Mass 380.14711772 g/mol
Topological Polar Surface Area (TPSA) 126.00 Ų
XlogP 0.10
Atomic LogP (AlogP) -0.43
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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CHEMBL483639
1-[(2S)-2-[3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-1-en-2-yl]-2,3-dihydro-1-benzofuran-5-yl]ethanone

2D Structure

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2D Structure of bitalin A-12-O-beta-D-glucopyranoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7577 75.77%
Caco-2 - 0.8205 82.05%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.7322 73.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8802 88.02%
OATP1B3 inhibitior + 0.9673 96.73%
MATE1 inhibitior - 0.9212 92.12%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7804 78.04%
P-glycoprotein inhibitior - 0.7167 71.67%
P-glycoprotein substrate - 0.7899 78.99%
CYP3A4 substrate + 0.5699 56.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8274 82.74%
CYP3A4 inhibition - 0.8254 82.54%
CYP2C9 inhibition - 0.8447 84.47%
CYP2C19 inhibition - 0.6078 60.78%
CYP2D6 inhibition - 0.8774 87.74%
CYP1A2 inhibition - 0.8125 81.25%
CYP2C8 inhibition - 0.5656 56.56%
CYP inhibitory promiscuity + 0.5974 59.74%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6263 62.63%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.9408 94.08%
Skin irritation - 0.7857 78.57%
Skin corrosion - 0.9393 93.93%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.5241 52.41%
Hepatotoxicity - 0.7747 77.47%
skin sensitisation - 0.7535 75.35%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.5206 52.06%
Acute Oral Toxicity (c) III 0.5495 54.95%
Estrogen receptor binding - 0.5223 52.23%
Androgen receptor binding - 0.5463 54.63%
Thyroid receptor binding + 0.5582 55.82%
Glucocorticoid receptor binding - 0.6233 62.33%
Aromatase binding + 0.6275 62.75%
PPAR gamma + 0.5746 57.46%
Honey bee toxicity - 0.8317 83.17%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7250 72.50%
Fish aquatic toxicity + 0.9731 97.31%

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 97.12% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.72% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.63% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.11% 99.17%
CHEMBL220 P22303 Acetylcholinesterase 90.91% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 88.34% 94.73%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.99% 95.89%
CHEMBL2581 P07339 Cathepsin D 87.03% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.29% 95.89%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.64% 96.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.87% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.59% 89.00%
CHEMBL4208 P20618 Proteasome component C5 82.77% 90.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.59% 97.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.35% 94.80%
CHEMBL3437 Q16853 Amine oxidase, copper containing 81.84% 94.00%
CHEMBL1951 P21397 Monoamine oxidase A 80.17% 91.49%

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.
Helichrysum italicum

Cross-Links

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PubChem 11079427
NPASS NPC238384
LOTUS LTS0045076
wikiData Q105264540