Marumoside A

Details

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Internal ID d8cf8f65-ed81-4d2a-a1f5-a9db0ea4119a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 2-[4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]acetamide
SMILES (Canonical) CC1C(C(C(C(O1)OC2=CC=C(C=C2)CC(=O)N)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=CC=C(C=C2)CC(=O)N)O)O)O
InChI InChI=1S/C14H19NO6/c1-7-11(17)12(18)13(19)14(20-7)21-9-4-2-8(3-5-9)6-10(15)16/h2-5,7,11-14,17-19H,6H2,1H3,(H2,15,16)/t7-,11-,12+,13+,14-/m0/s1
InChI Key FBANEUHXMFEIRO-WBFOWJMUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H19NO6
Molecular Weight 297.30 g/mol
Exact Mass 297.12123733 g/mol
Topological Polar Surface Area (TPSA) 122.00 Ų
XlogP -0.60
Atomic LogP (AlogP) -1.08
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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1309604-34-9
2-[4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]acetamide
AKOS040762026

2D Structure

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2D Structure of Marumoside A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6996 69.96%
Caco-2 - 0.5393 53.93%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.3891 38.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9581 95.81%
OATP1B3 inhibitior + 0.9338 93.38%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5859 58.59%
P-glycoprotein inhibitior - 0.9235 92.35%
P-glycoprotein substrate - 0.9179 91.79%
CYP3A4 substrate - 0.5188 51.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8597 85.97%
CYP3A4 inhibition - 0.8871 88.71%
CYP2C9 inhibition - 0.9325 93.25%
CYP2C19 inhibition - 0.9242 92.42%
CYP2D6 inhibition - 0.8793 87.93%
CYP1A2 inhibition - 0.9200 92.00%
CYP2C8 inhibition - 0.8122 81.22%
CYP inhibitory promiscuity - 0.8048 80.48%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8511 85.11%
Carcinogenicity (trinary) Non-required 0.5277 52.77%
Eye corrosion - 0.9941 99.41%
Eye irritation - 0.9711 97.11%
Skin irritation - 0.8038 80.38%
Skin corrosion - 0.9583 95.83%
Ames mutagenesis - 0.6228 62.28%
Human Ether-a-go-go-Related Gene inhibition - 0.7814 78.14%
Micronuclear + 0.7900 79.00%
Hepatotoxicity - 0.6697 66.97%
skin sensitisation - 0.8654 86.54%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.8923 89.23%
Acute Oral Toxicity (c) III 0.7141 71.41%
Estrogen receptor binding - 0.5565 55.65%
Androgen receptor binding - 0.7690 76.90%
Thyroid receptor binding - 0.5553 55.53%
Glucocorticoid receptor binding + 0.5754 57.54%
Aromatase binding - 0.5926 59.26%
PPAR gamma - 0.5458 54.58%
Honey bee toxicity - 0.9225 92.25%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6250 62.50%
Fish aquatic toxicity - 0.8386 83.86%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.79% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 94.65% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.54% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.62% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.94% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.91% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.82% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.69% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.37% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 87.37% 94.73%
CHEMBL4208 P20618 Proteasome component C5 86.97% 90.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 84.59% 97.36%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.25% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.09% 96.95%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.25% 95.89%

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.
Calamus draco
Excoecaria acerifolia
Garrya laurifolia
Goupia glabra
Laggera alata
Medinilla magnifica
Mesua ferrea
Moringa oleifera
Onobrychis bobrovii
Papaver persicum
Petteria ramentacea
Senecio cathcartensis
Sequoia sempervirens
Syncarpha gnaphaloides

Cross-Links

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PubChem 101794623
NPASS NPC187937
LOTUS LTS0045356
wikiData Q104992526