((1S,7AR)-hexahydro-1H-pyrrolizin-1-yl)methyl 4-(((2S,3R,4S,5S,6R)-3-(((2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)oxy)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-3,5-bis(3-methylbut-2-en-1-yl)benzoate

Details

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Internal ID 70a33dc6-db5b-4047-8195-a10bed048c2f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name [(1S,8R)-2,3,5,6,7,8-hexahydro-1H-pyrrolizin-1-yl]methyl 4-[(2S,3R,4S,5S,6R)-3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,5-bis(3-methylbut-2-enyl)benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C36H53NO12/c1-19(2)7-9-21-14-24(34(44)45-18-23-11-13-37-12-5-6-25(23)37)15-22(10-8-20(3)4)32(21)48-36-33(30(42)28(40)26(16-38)47-36)49-35-31(43)29(41)27(17-39)46-35/h7-8,14-15,23,25-31,33,35-36,38-43H,5-6,9-13,16-18H2,1-4H3/t23-,25-,26-,27+,28-,29+,30+,31-,33-,35+,36+/m1/s1
InChI Key LLZLNFVFAZZRDM-FRQBDSCNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C36H53NO12
Molecular Weight 691.80 g/mol
Exact Mass 691.35677613 g/mol
Topological Polar Surface Area (TPSA) 188.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 0.99
H-Bond Acceptor 13
H-Bond Donor 6
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of ((1S,7AR)-hexahydro-1H-pyrrolizin-1-yl)methyl 4-(((2S,3R,4S,5S,6R)-3-(((2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)oxy)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-3,5-bis(3-methylbut-2-en-1-yl)benzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8582 85.82%
Caco-2 - 0.8678 86.78%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.6959 69.59%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8514 85.14%
OATP1B3 inhibitior + 0.9224 92.24%
MATE1 inhibitior - 0.9212 92.12%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9309 93.09%
P-glycoprotein inhibitior + 0.6756 67.56%
P-glycoprotein substrate - 0.5790 57.90%
CYP3A4 substrate + 0.6337 63.37%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7950 79.50%
CYP3A4 inhibition - 0.9595 95.95%
CYP2C9 inhibition - 0.8812 88.12%
CYP2C19 inhibition - 0.9005 90.05%
CYP2D6 inhibition - 0.8250 82.50%
CYP1A2 inhibition - 0.7426 74.26%
CYP2C8 inhibition + 0.4520 45.20%
CYP inhibitory promiscuity - 0.8816 88.16%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5085 50.85%
Eye corrosion - 0.9875 98.75%
Eye irritation - 0.9261 92.61%
Skin irritation - 0.7741 77.41%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis - 0.7870 78.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7839 78.39%
Micronuclear + 0.7100 71.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.8412 84.12%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.8561 85.61%
Acute Oral Toxicity (c) III 0.6811 68.11%
Estrogen receptor binding + 0.7544 75.44%
Androgen receptor binding + 0.6587 65.87%
Thyroid receptor binding - 0.5603 56.03%
Glucocorticoid receptor binding + 0.5665 56.65%
Aromatase binding + 0.5949 59.49%
PPAR gamma + 0.6683 66.83%
Honey bee toxicity - 0.7996 79.96%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6055 60.55%
Fish aquatic toxicity + 0.9161 91.61%

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 97.49% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.55% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.72% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.48% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.22% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.11% 97.25%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 89.89% 95.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.17% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.03% 86.33%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 88.65% 83.57%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.10% 100.00%
CHEMBL4208 P20618 Proteasome component C5 87.02% 90.00%
CHEMBL5255 O00206 Toll-like receptor 4 86.72% 92.50%
CHEMBL3401 O75469 Pregnane X receptor 85.58% 94.73%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 84.79% 91.43%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.39% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.27% 99.17%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 84.13% 95.83%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.54% 89.00%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 83.23% 83.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.90% 93.04%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.99% 94.33%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.47% 96.61%

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.
Isodon nervosus

Cross-Links

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PubChem 134715008
LOTUS LTS0110527
wikiData Q104403051