Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C35H46O20 |
Molecular Weight | 786.7277 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 15 / 15 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OCCC3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2OC(=O)\C=C\C4=CC=C(O)C(O)=C4)[C@H](O[C@@H]5O[C@H](CO)[C@H](O)[C@H](O)[C@H]5O)[C@H](O)[C@H]1O
InChI
InChIKey=SDRRSTAVRUERNC-GUTOYVNHSA-N
InChI=1S/C35H46O20/c1-14-24(43)27(46)32(55-34-28(47)26(45)25(44)21(12-36)51-34)35(50-14)54-31-29(48)33(49-9-8-16-3-6-18(39)20(41)11-16)52-22(13-37)30(31)53-23(42)7-4-15-2-5-17(38)19(40)10-15/h2-7,10-11,14,21-22,24-41,43-48H,8-9,12-13H2,1H3/b7-4+/t14-,21+,22+,24-,25-,26-,27+,28+,29+,30+,31+,32+,33+,34-,35-/m0/s1
Molecular Formula | C35H46O20 |
Molecular Weight | 786.7277 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 15 / 15 |
E/Z Centers | 1 |
Optical Activity | UNSPECIFIED |
Teupolioside (known also as Lamiuside “A”) is a secondary metabolite produced by the Ajuga reptans plant for defensive purposes against environmental agents such as UV radiation. Teupolioside has shown a wide range of activities and it generally acts as an intinflammatory molecule. Moreover, Teupolioside is able to modulate testosterone-related disorders, like juvenile acne, and for the prevention of hair loss in androgenic alopecia. Specific in vitro and in vivo studies demonstrated that Teupolioside has beneficial effects also on other pathologic conditions such as: Benign prostatic hyperplasia (BPH), Crohn’s syndrome and other gastro-intestinal diseases, Microvasculature diseases.
Teupolioside exerts beneficial effects on a rodent model of colitis. Treatment with teupolioside significantly reduced the appearance of diarrhoea and the loss of body weight. This was associated with a remarkable amelioration in the disruption of the colonic architecture and a significant reduction in colonic myeloperoxidase activity and malondialdehyde levels. Teupolioside also reduced the pro-inflammatory cytokines release, the appearance of nitrotyrosine and PARP immunoreactivity in the colon and reduced the up-regulation of ICAM-1 and the expression of P-selectin. Therefore, teupolioside also reduced proMMP-9 and -2 activity induced in the colon by DNBS administration. Teupolioside-containing extracts significantly accelerated wound healing and possessed remarkable anti-inflammatory action in the excision wound model.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL3870 Sources: https://www.ncbi.nlm.nih.gov/pubmed/19070602 |
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Target ID: CHEMBL1075175 Sources: https://www.ncbi.nlm.nih.gov/pubmed/19070602 |
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Target ID: CHEMBL613712 Sources: https://www.ncbi.nlm.nih.gov/pubmed/17543237 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
|||
Sources: https://www.ncbi.nlm.nih.gov/pubmed/17543237 |
Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
Plant polyphenols effectively protect HaCaT cells from ultraviolet C-triggered necrosis and suppress inflammatory chemokine expression. | 2009 Aug |
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Teupolioside, a phenylpropanoid glycosides of Ajuga reptans, biotechnologically produced by IRBN22 plant cell line, exerts beneficial effects on a rodent model of colitis. | 2009 Mar 1 |
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Direct inhibition of calcineurin by caffeoyl phenylethanoid glycosides from Teucrium chamaedrys and Nepeta cataria. | 2011 Oct 11 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19070602
Rats: Teupolioside was administered daily orally (0.2 or 2mgkg(-1)).
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/17543237
Curator's Comment: Biotechnologically produced PPGs-containing extracts with different
concentrations of verbascoside (VB) and teupolioside (TP) were tested for their
superoxide, hydroxyl radical, and peroxynitrite scavenging activity in the cell-free systems generating ROS and RNS as well as for their ability to inhibiting Fe+2-induced lipid peroxidation and ROS release from the whole
blood leukocytes
97% teupolioside (TP) extract inhibited iron-induced linoleate peroxidation with IC50 value of 11.6 uM, effectively scavenged superoxide and
peroxynitrite (IC50 values of 1 ug/ml and 1.8 ug/ml, resp.)
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 01:31:28 GMT 2023
by
admin
on
Sat Dec 16 01:31:28 GMT 2023
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Record UNII |
88458S9198
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Record Status |
Validated (UNII)
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Record Version |
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-
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100000177490
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