T4309 |
CIL56
|
300802-28-2
|
99.91%
|
|
CIL56 (CA3) is a small molecule that induces cellular ferroptosis through the production of iron-dependent reactive oxygen species (ROS). It also induces accumul...
|
T6947 |
Piperlongumine
|
20069-09-4
|
99.89%
|
|
Piperlongumine (Piplartine) is a natural alkaloid from Piper longum L. It selectively kills cancer cells and strengthens the level of reactive oxygen species (RO...
|
T1630 |
Tiopronin
|
1953-02-2
|
99.87%
|
|
Tiopronin (Acadione), a sulfhydryl acylated derivative of glycine, leads to a reduction in urinary cystine concentration and subsequently reduces cystine stone f...
|
T4071 |
Repotrectinib
|
1802220-02-5
|
99.86%
|
|
Repotrectinib (TPX-0005) is a potent ALK/ROS1/TRK inhibitor, with IC50 of 1.01 nM, 5.3 nM, 1.08 nM and 1.26 nM for WT ALK, SRC, ALK L1196M and ALK G1202R, respec...
|
TN1949 |
Moracin C
|
69120-06-5
|
99.86%
|
|
Moracin C, a natural compound found in Morus mesozygia, Morus alba var. multicaulis, is an anti-inflammatory agent. moracin C inhibits nitric oxide (NO) release ...
|
T10668 |
Camalexin
|
135531-86-1
|
99.84%
|
|
Camalexin is a phytoalexin isolated from Camelina sativa. It has antifungal, antibacterial, antiproliferative, and anticancer activities. Camalexin can induce RO...
|
T2841 |
Plumbagin
|
481-42-5
|
99.82%
|
|
Plumbagin (Plumbaein) is a yellow dye, formally derived from naphthoquinone. It is named after the plant genus Plumbago, from which it was originally isolated. I...
|
T0437 |
Inosine
|
58-63-9
|
99.78%
|
|
Inosine (NSC-20262) is a purine nucleoside that has hypoxanthine linked by the N9 nitrogen to the C1 carbon of ribose. It has immunomodulatory, neuroprotective, ...
|
TN1725 |
Hederacolchiside E
|
33783-82-3
|
99.78%
|
|
Hederacolchiside E has antioxidant activity and shows neuroprotective effects in Alzheimer's disease (AD) models via modulating oxidative stress. Hederacolchisid...
|
T23046 |
N-tert-butyl-α-Phenylnitrone
|
3376-24-7
|
99.69%
|
|
N-tert-butyl-α-Phenylnitrone ((Z)-N-benzylidene-2-Methylpropan-2-aMine oxide) inhibits COX2 catalytic activity. N-tert-butyl-α-Phenylnitrone((Z)-N-benzylidene-2-...
|
T8255 |
(±)-Catechin
|
7295-85-4
|
99.69%
|
|
(±)-Catechin ((±)-Catechin hydrate) hydrate is a natural product,has antioxidant activity and is effective in reducing oxidative stress.
|
T24865 |
Tenivastatin
|
121009-77-6
|
99.68%
|
|
Tenivastatin (Simvastatin acid) is an anti-hyperlipidemic HMG-CoA reductase inhibitor that inhibits the production of reactive oxygen species (ROS) and can be us...
|
TN1146 |
8-Prenylnaringenin
|
53846-50-7
|
99.67%
|
|
8-Prenylnaringenin is a phytoestrogen with high estrogenic activity,
|
T8399 |
Crizotinib hydrochloride
|
1415560-69-8
|
99.67%
|
|
Crizotinib hydrochloride (PF-02341066 hydrochloride) is a novel inhibitor of anaplastic lymphoma kinase and c-Met(IC50s of 20 and 8 nM)
|
TN1721 |
Gypenoside L
|
94987-09-4
|
99.65%
|
|
Gypenoside L inhibits autophagic flux and induces cell death in human esophageal cancer cells through endoplasm reticulum stress-mediated Ca2+ release. It also i...
|
T3678 |
Entrectinib
|
1108743-60-7
|
99.61%
|
|
Entrectinib (RXDX-101) is an inhibitor of TrkA (IC50: 1.7 nM), TrkB (IC50: 0.1 nM), and TrkC (IC50: 0.1 nM), as well as anaplastic lymphoma kinase (ALK; IC50: 1....
|
T3455 |
Merestinib
|
1206799-15-6
|
99.56%
|
|
Merestinib (LY2801653) is an orally available, small molecule inhibitor of the proto-oncogene c-Met (Ki: 2 nM) with potential antineoplastic activity. Merestinib...
|
T3415 |
Secoisolariciresinol diglucoside
|
158932-33-3
|
99.54%
|
|
Secoisolariciresinol diglucoside (LGM2605) was cytoprotective in an in vitro model of iron overload-induced redox-inflammatory damage. Secoisolariciresinol diglu...
|
T3S1692 |
Octahydrocurcumin
|
36062-07-4
|
99.54%
|
|
Octahydrocurcumin has antioxidant and and anti-inflammatory activities, it can inhibit the lipopolysaccharide (LPS)-induced inflammatory response via the mechani...
|
TN1731 |
Hernandezine
|
6681-13-6
|
99.53%
|
|
Hernandezine is an activator of AMPK activator and a selective reversing agent for ABCB1-mediated MDR in cancer cells.
|