[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 2-(6'-ethenyl-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl)-3-methoxyprop-2-enoate

Details

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Internal ID 4d2a6281-999d-49d5-a7e8-25420faf0586
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Hexoses
IUPAC Name [3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 2-(6'-ethenyl-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl)-3-methoxyprop-2-enoate
SMILES (Canonical) COC=C(C1CC2C3(CCN2CC1C=C)C4=CC=CC=C4NC3=O)C(=O)OC5C(C(C(C(O5)CO)O)O)O
SMILES (Isomeric) COC=C(C1CC2C3(CCN2CC1C=C)C4=CC=CC=C4NC3=O)C(=O)OC5C(C(C(C(O5)CO)O)O)O
InChI InChI=1S/C27H34N2O9/c1-3-14-11-29-9-8-27(17-6-4-5-7-18(17)28-26(27)35)20(29)10-15(14)16(13-36-2)24(34)38-25-23(33)22(32)21(31)19(12-30)37-25/h3-7,13-15,19-23,25,30-33H,1,8-12H2,2H3,(H,28,35)
InChI Key BBUOHZFHYRHXQC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H34N2O9
Molecular Weight 530.60 g/mol
Exact Mass 530.22643067 g/mol
Topological Polar Surface Area (TPSA) 158.00 Ų
XlogP -0.10
Atomic LogP (AlogP) -0.35
H-Bond Acceptor 10
H-Bond Donor 5
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 2-(6'-ethenyl-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl)-3-methoxyprop-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6109 61.09%
Caco-2 - 0.8379 83.79%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6624 66.24%
OATP2B1 inhibitior - 0.8614 86.14%
OATP1B1 inhibitior + 0.8742 87.42%
OATP1B3 inhibitior + 0.9335 93.35%
MATE1 inhibitior - 0.8420 84.20%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8588 85.88%
P-glycoprotein inhibitior + 0.6111 61.11%
P-glycoprotein substrate + 0.5384 53.84%
CYP3A4 substrate + 0.7156 71.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8175 81.75%
CYP3A4 inhibition - 0.8353 83.53%
CYP2C9 inhibition - 0.7763 77.63%
CYP2C19 inhibition - 0.8686 86.86%
CYP2D6 inhibition - 0.8899 88.99%
CYP1A2 inhibition - 0.8214 82.14%
CYP2C8 inhibition + 0.5158 51.58%
CYP inhibitory promiscuity - 0.9079 90.79%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4993 49.93%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.9671 96.71%
Skin irritation - 0.7583 75.83%
Skin corrosion - 0.9305 93.05%
Ames mutagenesis - 0.6944 69.44%
Human Ether-a-go-go-Related Gene inhibition + 0.7753 77.53%
Micronuclear + 0.8900 89.00%
Hepatotoxicity - 0.5841 58.41%
skin sensitisation - 0.8503 85.03%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity + 0.5466 54.66%
Acute Oral Toxicity (c) III 0.5836 58.36%
Estrogen receptor binding + 0.7727 77.27%
Androgen receptor binding + 0.7009 70.09%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.5930 59.30%
Aromatase binding - 0.4935 49.35%
PPAR gamma + 0.6426 64.26%
Honey bee toxicity - 0.7322 73.22%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.8808 88.08%

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 98.70% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.56% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.36% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.47% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.52% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.27% 97.09%
CHEMBL4208 P20618 Proteasome component C5 90.12% 90.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 88.44% 94.08%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.71% 90.71%
CHEMBL1937 Q92769 Histone deacetylase 2 87.13% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.54% 99.23%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.83% 96.47%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.12% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.81% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.67% 94.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.17% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.46% 85.14%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.17% 93.00%
CHEMBL5028 O14672 ADAM10 80.42% 97.50%

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.
Uncaria rhynchophylla

Cross-Links

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PubChem 74976277
LOTUS LTS0255642
wikiData Q104923071