Ranunculin

Details

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Internal ID 09215fd1-f792-4a30-a934-abb836c731af
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name (2S)-2-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-2H-furan-5-one
SMILES (Canonical) C1=CC(=O)OC1COC2C(C(C(C(O2)CO)O)O)O
SMILES (Isomeric) C1=CC(=O)O[C@@H]1CO[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O
InChI InChI=1S/C11H16O8/c12-3-6-8(14)9(15)10(16)11(19-6)17-4-5-1-2-7(13)18-5/h1-2,5-6,8-12,14-16H,3-4H2/t5-,6+,8+,9-,10+,11+/m0/s1
InChI Key TYWXNGXVSZRXNA-NVZSGMJQSA-N
Popularity 97 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16O8
Molecular Weight 276.24 g/mol
Exact Mass 276.08451746 g/mol
Topological Polar Surface Area (TPSA) 126.00 Ų
XlogP -2.00
Atomic LogP (AlogP) -2.72
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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644-69-9
UNII-IBP7446K1O
IBP7446K1O
EINECS 211-421-6
NSC 616960
(S)-5-((beta-D-Glucopyranosyloxy)methyl)furan-2(5H)-one
C08512
(S)-5-[(beta-D-Glucopyranosyloxy)methyl]furan-2(5H)-one
(S)-5-((((2R,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)methyl)furan-2(5H)-one
AC1L9BCS
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ranunculin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8615 86.15%
Caco-2 - 0.8644 86.44%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.7767 77.67%
OATP2B1 inhibitior - 0.8577 85.77%
OATP1B1 inhibitior + 0.8458 84.58%
OATP1B3 inhibitior + 0.9637 96.37%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9090 90.90%
P-glycoprotein inhibitior - 0.9532 95.32%
P-glycoprotein substrate - 0.9694 96.94%
CYP3A4 substrate - 0.5345 53.45%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8854 88.54%
CYP3A4 inhibition - 0.9573 95.73%
CYP2C9 inhibition - 0.9541 95.41%
CYP2C19 inhibition - 0.9132 91.32%
CYP2D6 inhibition - 0.9265 92.65%
CYP1A2 inhibition - 0.9370 93.70%
CYP2C8 inhibition - 0.9297 92.97%
CYP inhibitory promiscuity - 0.8557 85.57%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7026 70.26%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.9566 95.66%
Skin irritation - 0.8559 85.59%
Skin corrosion - 0.9469 94.69%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6570 65.70%
Micronuclear - 0.8341 83.41%
Hepatotoxicity - 0.7571 75.71%
skin sensitisation - 0.9125 91.25%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.5938 59.38%
Acute Oral Toxicity (c) IV 0.4721 47.21%
Estrogen receptor binding - 0.8044 80.44%
Androgen receptor binding - 0.7205 72.05%
Thyroid receptor binding - 0.7166 71.66%
Glucocorticoid receptor binding + 0.5400 54.00%
Aromatase binding - 0.5471 54.71%
PPAR gamma - 0.5386 53.86%
Honey bee toxicity - 0.8357 83.57%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7450 74.50%
Fish aquatic toxicity - 0.7350 73.50%

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 98.02% 91.11%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 89.83% 86.92%
CHEMBL2581 P07339 Cathepsin D 87.67% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 86.52% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.50% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.71% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.69% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.36% 97.09%

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.
Actaea rubra
Caltha palustris
Pulsatilla chinensis
Ranunculus pinguis
Ranunculus sceleratus

Cross-Links

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PubChem 441581
NPASS NPC42937
LOTUS LTS0141949
wikiData Q1245911