T2794 |
Astilbin
|
29838-67-3
|
98%
|
|
Astilbin is actions Flavonoid phytochemical found in St. John′s wort and Traditional Chinese Medicine herbal preparations.
|
T2932 |
Ginsenoside Rh1
|
63223-86-9
|
98%
|
|
Ginsenoside Rg1, one of the main constituents of Panax ginseng, exhibits anti-inflammatory effect.
|
TN2079 |
(-)-Pinoresinol
|
81446-29-9
|
98%
|
|
(-)-Pinoresinol is isolated from the whole plant of Serissa japonica (Thunb.) Thunb.
|
T3770 |
Taraxasterol
|
1059-14-9
|
98%
|
|
Taraxasterol is compound with anti-inflammatory activity.
|
T2065 |
Bioymifi
|
1420071-30-2
|
98%
|
|
Bioymifi is a novel and potent small-molecule activator of the TRAIL receptor DR5 in human cancer cells.
|
TN1295 |
5-O-Caffeoylshikimic acid
|
73263-62-4
|
98%
|
|
5-O-Caffeoylshikimic acid shows anti-oxidative activity; it also shows anti-inflammatory activity, the underlying mechanism was associated with downregulation of...
|
TN3609 |
Catalposide
|
6736-85-2
|
98%
|
|
Catalposide is a potent inducer of (HO)-1 isolated from Catalpa ovate G. Don (Bignoniaceae). Catalposide possesses antioxidant, anti-apoptotic, anti-microbial, a...
|
T5S1632 |
Barlerin
|
57420-46-9
|
98%
|
|
8-O-Acetylshanzhiside methylester has potential against cerebral ischemic injury, and its protective effect on oxygen-glucose deprivation-induced injury might be...
|
T5788 |
XYLOBIOSE
|
6860-47-5
|
98%
|
|
XYLOBIOSE ia a natural product,and exhibited therapeutic potential for treating obesity which involved suppression of fat deposition and obesity-related metaboli...
|
T0694 |
Pranlukast
|
103177-37-3
|
98%
|
|
Pranlukast is a cysteinyl leukotriene receptor-1 antagonist. It antagonizes or reduces bronchospasm caused, principally in asthmatics, by an allergic reaction to...
|
T2A2481 |
Taurochenodeoxycholic Acid
|
516-35-8
|
98%
|
|
Taurochenodeoxycholic acid is one of the main bioactive substances of animals' bile acid.
|
T1265 |
Amrinone
|
60719-84-8
|
98%
|
|
Amrinone is a positive inotropic cardiotonic (cardiotonic agent) with vasodilator properties, phosphodiesterase 3 inhibitory activity.
|
T1813 |
VGX-1027
|
6501-72-0
|
98%
|
|
VGX-1027(GIT27) is an isoxazole compound with various immunomodulatory properties.
|
T6204 |
QNZ
|
545380-34-5
|
98%
|
|
QNZ (EVP4593) is an effective inhibitor of NF-κB activation and TNF-α production. The IC50 of QNZ for NF-κB and TNF-α is11 nM and 7 nM, respectively.
|
T4450 |
GIBH-130
|
1252608-59-5
|
98%
|
|
GIBH-130 markedly inhibits the IL-1β secretion by activated microglia (IC50: 3.4 nM). GIBH-130 is an effective inhibitor of neuroinflammation.
|
T0213 |
Thalidomide
|
50-35-1
|
98%
|
|
Thalidomide is a synthetic derivative of glutamic acid (alpha-phthalimido-glutarimide) with teratogenic, immunomodulatory, anti-inflammatory and anti-angiogenic ...
|
T0304 |
Methylthiouracil
|
56-04-2
|
98%
|
|
Methylthiouracil is a thiourea antithyroid agent that inhibits the synthesis of thyroid hormone, and it is used to treat hyperthyroidism.
|
T61111 |
UCB-5307
|
1515887-44-1
|
98%
|
|
UCB-5307 is a small molecule compound that inhibits TNFR1 signal transduction and downstream function in vitro. The KD of human TNFα is 9 nM. The TNF was directl...
|
T4403 |
AX-024 hydrochloride
|
1704801-24-0
|
98%
|
|
AX-024 hydrochloride is an cytokine release inhibitor which can strongly inhibit the production of interleukin-6 (IL-6), tumor necrosis factor-α (TNFα), interfer...
|
T1125 |
Shikonin
|
517-89-5
|
98%
|
|
Shikonin is an TMEM16A chloride channel inhibitor (IC50: 6.5 μM). Shikonin is also a selective PKM2 inhibitor and can also suppress activation of the NF-κB pathw...
|