Deoxypentalenylglucuron

Details

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Internal ID a6e5c840-e320-4337-9cdf-26960ce53e6a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name (2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-[(1R,2R,5R,8S)-2,10,10-trimethyltricyclo[6.3.0.01,5]undec-6-ene-6-carbonyl]oxyoxane-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H30O8/c1-9-4-5-12-11(6-10-7-20(2,3)8-21(9,10)12)18(27)29-19-15(24)13(22)14(23)16(28-19)17(25)26/h6,9-10,12-16,19,22-24H,4-5,7-8H2,1-3H3,(H,25,26)/t9-,10-,12+,13+,14+,15+,16+,19+,21-/m1/s1
InChI Key BFYOGFPGIVIQCC-UPUKJNKPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H30O8
Molecular Weight 410.50 g/mol
Exact Mass 410.19406791 g/mol
Topological Polar Surface Area (TPSA) 134.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 0.83
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Deoxypentalenylglucuron

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8861 88.61%
Caco-2 - 0.8341 83.41%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7400 74.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8934 89.34%
OATP1B3 inhibitior + 0.9050 90.50%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9729 97.29%
P-glycoprotein inhibitior - 0.7143 71.43%
P-glycoprotein substrate - 0.7974 79.74%
CYP3A4 substrate + 0.6142 61.42%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8834 88.34%
CYP3A4 inhibition - 0.8264 82.64%
CYP2C9 inhibition - 0.7618 76.18%
CYP2C19 inhibition - 0.8436 84.36%
CYP2D6 inhibition - 0.9295 92.95%
CYP1A2 inhibition - 0.6421 64.21%
CYP2C8 inhibition + 0.4747 47.47%
CYP inhibitory promiscuity - 0.9244 92.44%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6555 65.55%
Eye corrosion - 0.9876 98.76%
Eye irritation - 0.9191 91.91%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9180 91.80%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5148 51.48%
Micronuclear - 0.7900 79.00%
Hepatotoxicity - 0.6227 62.27%
skin sensitisation - 0.7272 72.72%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8269 82.69%
Acute Oral Toxicity (c) III 0.3553 35.53%
Estrogen receptor binding + 0.7313 73.13%
Androgen receptor binding + 0.5904 59.04%
Thyroid receptor binding - 0.4881 48.81%
Glucocorticoid receptor binding - 0.5730 57.30%
Aromatase binding + 0.5498 54.98%
PPAR gamma + 0.6327 63.27%
Honey bee toxicity - 0.8474 84.74%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9891 98.91%

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 97.30% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.88% 91.11%
CHEMBL5255 O00206 Toll-like receptor 4 84.82% 92.50%
CHEMBL2581 P07339 Cathepsin D 84.59% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.10% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.07% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.79% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.63% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.01% 94.45%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.38% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.76% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139589056
LOTUS LTS0157500
wikiData Q104935053