Unedide

Details

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Internal ID 95577f86-0cec-4851-8a1d-639f45ce3312
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Iridoid O-glycosides
IUPAC Name (1S,4aS,5R,7R,7aS)-5,7-dihydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid
SMILES (Canonical) C1C(C2C(C1(CO)O)C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O
SMILES (Isomeric) C1[C@H]([C@H]2[C@@H]([C@]1(CO)O)[C@@H](OC=C2C(=O)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O
InChI InChI=1S/C16H24O12/c17-2-7-10(20)11(21)12(22)15(27-7)28-14-9-8(5(3-26-14)13(23)24)6(19)1-16(9,25)4-18/h3,6-12,14-15,17-22,25H,1-2,4H2,(H,23,24)/t6-,7-,8+,9-,10-,11+,12-,14+,15+,16+/m1/s1
InChI Key YEOAKYNPUWNNOB-KDYWOABDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H24O12
Molecular Weight 408.35 g/mol
Exact Mass 408.12677620 g/mol
Topological Polar Surface Area (TPSA) 207.00 Ų
XlogP -4.00
Atomic LogP (AlogP) -4.15
H-Bond Acceptor 11
H-Bond Donor 8
Rotatable Bonds 5

Synonyms

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80666-55-3

2D Structure

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2D Structure of Unedide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5000 50.00%
Caco-2 - 0.9127 91.27%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.6372 63.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7725 77.25%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9588 95.88%
P-glycoprotein inhibitior - 0.8993 89.93%
P-glycoprotein substrate - 0.8611 86.11%
CYP3A4 substrate + 0.5745 57.45%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8755 87.55%
CYP3A4 inhibition - 0.9545 95.45%
CYP2C9 inhibition - 0.9185 91.85%
CYP2C19 inhibition - 0.8350 83.50%
CYP2D6 inhibition - 0.8851 88.51%
CYP1A2 inhibition - 0.8970 89.70%
CYP2C8 inhibition - 0.7493 74.93%
CYP inhibitory promiscuity - 0.8723 87.23%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6552 65.52%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.9473 94.73%
Skin irritation - 0.7687 76.87%
Skin corrosion - 0.9480 94.80%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6633 66.33%
Micronuclear - 0.7141 71.41%
Hepatotoxicity - 0.9214 92.14%
skin sensitisation - 0.8533 85.33%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.6312 63.12%
Acute Oral Toxicity (c) III 0.3695 36.95%
Estrogen receptor binding + 0.5524 55.24%
Androgen receptor binding - 0.5522 55.22%
Thyroid receptor binding - 0.5209 52.09%
Glucocorticoid receptor binding - 0.6295 62.95%
Aromatase binding + 0.6832 68.32%
PPAR gamma + 0.6147 61.47%
Honey bee toxicity - 0.8040 80.40%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6950 69.50%
Fish aquatic toxicity - 0.5706 57.06%

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 96.91% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.38% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.60% 97.09%
CHEMBL4208 P20618 Proteasome component C5 89.30% 90.00%
CHEMBL220 P22303 Acetylcholinesterase 89.05% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 88.44% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.72% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.08% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.07% 96.95%
CHEMBL218 P21554 Cannabinoid CB1 receptor 82.52% 96.61%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.09% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.71% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.21% 89.00%
CHEMBL1811 P34995 Prostanoid EP1 receptor 80.10% 95.71%

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.
Arbutus unedo

Cross-Links

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PubChem 101286277
NPASS NPC265057
LOTUS LTS0029600
wikiData Q105347329