Drabanemoroside

Details

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Internal ID a76e4bf5-076c-4a5f-8a44-c134e9f92bbc
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-3-O-glycosides
IUPAC Name 3-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H28O14/c1-9-17(31)20(34)21(35)25(37-9)40-24-18(32)14(30)8-36-26(24)39-23-19(33)16-13(29)6-12(28)7-15(16)38-22(23)10-2-4-11(27)5-3-10/h2-7,9,14,17-18,20-21,24-32,34-35H,8H2,1H3/t9-,14-,17-,18-,20+,21+,24+,25-,26-/m0/s1
InChI Key IQYYAZNEJJZDLV-LFKMRFHZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H28O14
Molecular Weight 564.50 g/mol
Exact Mass 564.14790556 g/mol
Topological Polar Surface Area (TPSA) 225.00 Ų
XlogP -0.30
Atomic LogP (AlogP) -0.75
H-Bond Acceptor 14
H-Bond Donor 8
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Drabanemoroside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8527 85.27%
Caco-2 - 0.9131 91.31%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.6889 68.89%
OATP2B1 inhibitior - 0.5589 55.89%
OATP1B1 inhibitior + 0.8852 88.52%
OATP1B3 inhibitior - 0.2426 24.26%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8904 89.04%
P-glycoprotein inhibitior - 0.5998 59.98%
P-glycoprotein substrate + 0.6111 61.11%
CYP3A4 substrate + 0.6761 67.61%
CYP2C9 substrate - 0.7354 73.54%
CYP2D6 substrate - 0.8607 86.07%
CYP3A4 inhibition - 0.9257 92.57%
CYP2C9 inhibition - 0.9669 96.69%
CYP2C19 inhibition - 0.9421 94.21%
CYP2D6 inhibition - 0.9556 95.56%
CYP1A2 inhibition - 0.8839 88.39%
CYP2C8 inhibition + 0.7972 79.72%
CYP inhibitory promiscuity - 0.9036 90.36%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6732 67.32%
Eye corrosion - 0.9918 99.18%
Eye irritation - 0.9007 90.07%
Skin irritation - 0.7776 77.76%
Skin corrosion - 0.9503 95.03%
Ames mutagenesis + 0.5563 55.63%
Human Ether-a-go-go-Related Gene inhibition - 0.4738 47.38%
Micronuclear + 0.7633 76.33%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8964 89.64%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.9252 92.52%
Acute Oral Toxicity (c) III 0.6152 61.52%
Estrogen receptor binding + 0.8054 80.54%
Androgen receptor binding + 0.6886 68.86%
Thyroid receptor binding + 0.5575 55.75%
Glucocorticoid receptor binding + 0.6205 62.05%
Aromatase binding + 0.6190 61.90%
PPAR gamma + 0.7398 73.98%
Honey bee toxicity - 0.7423 74.23%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5050 50.50%
Fish aquatic toxicity + 0.8497 84.97%

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 99.46% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.94% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 98.20% 89.00%
CHEMBL2581 P07339 Cathepsin D 97.48% 98.95%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 96.96% 95.64%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.47% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.08% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.39% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 89.82% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.82% 95.56%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 87.01% 95.78%
CHEMBL4208 P20618 Proteasome component C5 86.11% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.51% 96.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.30% 97.36%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.40% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.95% 99.23%
CHEMBL2842 P42345 Serine/threonine-protein kinase mTOR 82.46% 92.78%
CHEMBL1937 Q92769 Histone deacetylase 2 81.95% 94.75%
CHEMBL3194 P02766 Transthyretin 80.99% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.24% 99.17%

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.
Lobularia maritima

Cross-Links

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PubChem 163010372
LOTUS LTS0108575
wikiData Q105118712