[5-Hydroxy-2-[6-[4-hydroxy-6-[4-methoxy-6-(4-methoxy-2-methyl-6-oxooxan-3-yl)oxy-2-methyloxan-3-yl]oxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-6-methyloxan-3-yl] acetate

Details

Top
Internal ID d4f8b3cd-304c-409f-a1f4-d76c6d10b7c7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Oligosaccharides
IUPAC Name [5-hydroxy-2-[6-[4-hydroxy-6-[4-methoxy-6-(4-methoxy-2-methyl-6-oxooxan-3-yl)oxy-2-methyloxan-3-yl]oxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-6-methyloxan-3-yl] acetate
SMILES (Canonical) CC1C(C(C(C(O1)OC2C(OC(CC2OC)OC3C(OC(CC3O)OC4C(OC(CC4OC)OC5C(OC(=O)CC5OC)C)C)C)C)OC(=O)C)OC)O
SMILES (Isomeric) CC1C(C(C(C(O1)OC2C(OC(CC2OC)OC3C(OC(CC3O)OC4C(OC(CC4OC)OC5C(OC(=O)CC5OC)C)C)C)C)OC(=O)C)OC)O
InChI InChI=1S/C36H60O18/c1-15-29(40)34(44-10)35(50-20(6)37)36(49-15)54-33-19(5)48-27(14-24(33)43-9)51-30-16(2)46-26(11-21(30)38)52-32-18(4)47-28(13-23(32)42-8)53-31-17(3)45-25(39)12-22(31)41-7/h15-19,21-24,26-36,38,40H,11-14H2,1-10H3
InChI Key FIUKBOHZSAVHEV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C36H60O18
Molecular Weight 780.80 g/mol
Exact Mass 780.37796506 g/mol
Topological Polar Surface Area (TPSA) 204.00 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.73
H-Bond Acceptor 18
H-Bond Donor 2
Rotatable Bonds 13

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of [5-Hydroxy-2-[6-[4-hydroxy-6-[4-methoxy-6-(4-methoxy-2-methyl-6-oxooxan-3-yl)oxy-2-methyloxan-3-yl]oxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-6-methyloxan-3-yl] acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7895 78.95%
Caco-2 - 0.8456 84.56%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6930 69.30%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8488 84.88%
OATP1B3 inhibitior + 0.8801 88.01%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8808 88.08%
P-glycoprotein inhibitior + 0.7334 73.34%
P-glycoprotein substrate - 0.5373 53.73%
CYP3A4 substrate + 0.6543 65.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8988 89.88%
CYP3A4 inhibition - 0.9644 96.44%
CYP2C9 inhibition - 0.9787 97.87%
CYP2C19 inhibition - 0.9742 97.42%
CYP2D6 inhibition - 0.9240 92.40%
CYP1A2 inhibition - 0.9641 96.41%
CYP2C8 inhibition - 0.8231 82.31%
CYP inhibitory promiscuity - 0.9781 97.81%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6221 62.21%
Eye corrosion - 0.9708 97.08%
Eye irritation - 0.9057 90.57%
Skin irritation - 0.7676 76.76%
Skin corrosion - 0.9384 93.84%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4373 43.73%
Micronuclear + 0.5200 52.00%
Hepatotoxicity - 0.5050 50.50%
skin sensitisation - 0.9374 93.74%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.6251 62.51%
Acute Oral Toxicity (c) III 0.6708 67.08%
Estrogen receptor binding + 0.7283 72.83%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.5683 56.83%
Glucocorticoid receptor binding + 0.6832 68.32%
Aromatase binding + 0.6046 60.46%
PPAR gamma + 0.6617 66.17%
Honey bee toxicity - 0.6499 64.99%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.6247 62.47%

Targets

Top

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 95.61% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.21% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.67% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.37% 89.00%
CHEMBL340 P08684 Cytochrome P450 3A4 89.10% 91.19%
CHEMBL2581 P07339 Cathepsin D 88.63% 98.95%
CHEMBL3714130 P46095 G-protein coupled receptor 6 88.49% 97.36%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.33% 99.23%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.13% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.29% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.38% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.26% 95.56%
CHEMBL5255 O00206 Toll-like receptor 4 81.53% 92.50%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 81.20% 83.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.35% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 80.10% 94.73%

Plants that contains it

Top
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.
Periploca sepium

Cross-Links

Top
PubChem 74397826
LOTUS LTS0004247
wikiData Q104995880