9,15,16,17,20,21,33,34,35,38,39,42,43,44-Tetradecahydroxy-5,8,11,26,29,40,48-heptaoxanonacyclo[20.17.9.03,37.07,28.010,27.013,18.019,24.031,36.041,46]octatetraconta-1(39),2,13,15,17,19,21,23,31,33,35,37,41,43,45-pentadecaene-4,12,25,30,47-pentone

Details

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Internal ID ffdac2ff-0519-4dd1-b051-cf30ebc9b99c
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name 9,15,16,17,20,21,33,34,35,38,39,42,43,44-tetradecahydroxy-5,8,11,26,29,40,48-heptaoxanonacyclo[20.17.9.03,37.07,28.010,27.013,18.019,24.031,36.041,46]octatetraconta-1(39),2,13,15,17,19,21,23,31,33,35,37,41,43,45-pentadecaene-4,12,25,30,47-pentone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C41H26O26/c42-12-1-7-18(27(50)22(12)45)20-9-4-15(25(48)29(20)52)62-32-11(3-14(44)24(47)31(32)54)40(59)63-16-5-10-21(30(53)26(16)49)19-8(2-13(43)23(46)28(19)51)38(57)67-35-34(66-39(10)58)33(65-37(7)56)17(64-41(35)60)6-61-36(9)55/h1-5,17,33-35,41-54,60H,6H2
InChI Key SGLHXMXIRRTFQB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C41H26O26
Molecular Weight 934.60 g/mol
Exact Mass 934.07123093 g/mol
Topological Polar Surface Area (TPSA) 433.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.70
H-Bond Acceptor 26
H-Bond Donor 14
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9,15,16,17,20,21,33,34,35,38,39,42,43,44-Tetradecahydroxy-5,8,11,26,29,40,48-heptaoxanonacyclo[20.17.9.03,37.07,28.010,27.013,18.019,24.031,36.041,46]octatetraconta-1(39),2,13,15,17,19,21,23,31,33,35,37,41,43,45-pentadecaene-4,12,25,30,47-pentone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5693 56.93%
Caco-2 - 0.8973 89.73%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5861 58.61%
OATP2B1 inhibitior - 0.5667 56.67%
OATP1B1 inhibitior + 0.8280 82.80%
OATP1B3 inhibitior + 0.9673 96.73%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9271 92.71%
P-glycoprotein inhibitior + 0.7159 71.59%
P-glycoprotein substrate - 0.7297 72.97%
CYP3A4 substrate + 0.5965 59.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8493 84.93%
CYP3A4 inhibition - 0.8649 86.49%
CYP2C9 inhibition - 0.7987 79.87%
CYP2C19 inhibition - 0.9089 90.89%
CYP2D6 inhibition - 0.9212 92.12%
CYP1A2 inhibition - 0.8636 86.36%
CYP2C8 inhibition - 0.5828 58.28%
CYP inhibitory promiscuity - 0.9469 94.69%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7012 70.12%
Eye corrosion - 0.9928 99.28%
Eye irritation - 0.8805 88.05%
Skin irritation - 0.7337 73.37%
Skin corrosion - 0.9398 93.98%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7300 73.00%
Micronuclear + 0.7633 76.33%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.8462 84.62%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7854 78.54%
Acute Oral Toxicity (c) III 0.3250 32.50%
Estrogen receptor binding + 0.8133 81.33%
Androgen receptor binding + 0.6977 69.77%
Thyroid receptor binding - 0.4905 49.05%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.5308 53.08%
PPAR gamma + 0.7040 70.40%
Honey bee toxicity - 0.7997 79.97%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.8783 87.83%

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 98.83% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.81% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.34% 89.00%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 92.74% 83.57%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.86% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.89% 93.40%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.02% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.52% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.72% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 87.69% 94.73%
CHEMBL2581 P07339 Cathepsin D 86.31% 98.95%
CHEMBL4208 P20618 Proteasome component C5 82.69% 90.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.06% 100.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.96% 94.80%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.12% 86.33%
CHEMBL3137261 O14744 PRMT5/MEP50 complex 80.95% 100.00%

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.
Stachyurus praecox

Cross-Links

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PubChem 163084428
LOTUS LTS0019764
wikiData Q105252393