T14034 |
3CAI
|
28755-03-5
|
98%
|
|
3CAI is a potent and specific AKT1 and AKT2 inhibitor which showed significant inhibition of AKT in an in vitro kinase assay and suppressed expression of AKT dir...
|
T6252 |
Ipatasertib
|
1001264-89-6
|
98%
|
|
Ipatasertib (GDC-0068), a highly specific pan-Akt inhibitor, targets Akt1/2/3 with IC50 of 5 nM/18 nM/8 nM, respectively.
|
T3P2904 |
α-Linolenic acid
|
463-40-1
|
98%
|
|
Linolenic Acid is an essential fatty acid belonging to the omega-3 fatty acids group. It is highly concentrated in certain plant oils and has been reported to in...
|
T0228 |
Methyl-Hesperidin
|
11013-97-1
|
98%
|
|
Methyl Hesperidin, a flavanone glycoside (flavonoid) (C28H34O15), is abundant in citrus fruits. Its aglycone form is called hesperetin.
|
T2S1040 |
Jolkinolide B
|
37905-08-1
|
98%
|
|
Jolkinolide B is a bioactive diterpene isolated from the roots of Euphorbia fischeriana Steud. Jolkinolide B induces apoptosis in cancer cells. Jolkinolide B can...
|
T4046 |
BX517
|
850717-64-5
|
98%
|
|
BX-517 is a potent and selective inhibitor of PDK1.
|
T14072 |
A-443654
|
552325-16-3
|
98%
|
|
A-443654 is a pan-Akt inhibitor. It has equal potency against Akt1, Akt2, or Akt3 within cells (Ki=160 pM).
|
T4489 |
AKT-IN-1
|
1357158-81-6
|
98%
|
|
AZD-26 is an allosteric AKT inhibitor (IC50: 1.04 μM).
|
T15469 |
Hematein
|
475-25-2
|
98%
|
|
Hematein inhibits Akt/PKB Ser129 phosphorylation, the Wnt/TCF pathway, and increases apoptosis in lung cancer cells. Hematein is an oxidation product of hematoxy...
|
T9831 |
MKC-1
|
125313-92-0
|
98%
|
|
MKC-1 is an orally bioavailable, small-molecule, bisindolylmaleimide cell cycle inhibitor with potential antineoplastic activity. MKC-1 and its metabolites inhib...
|
T5S0168 |
Atractylenolide II
|
73069-14-4
|
98%
|
|
1. Atractylenolide II has antimelanoma effect by inhibiting STAT3 signalling. 2. Atractylenolide II has cytotoxic/apoptotic effects may via p38 activation , ERK ...
|
T15374 |
Ipatasertib dihydrochloride
|
1396257-94-5
|
98%
|
|
Ipatasertib dihydrochloride is a highly selective and ATP-competitive inhibitor of pan-Akt (IC50s: 5, 18, and 8 nM for Akt1, Akt2, and Akt3, respectively).
|
T4444 |
A-674563 HCl (552325-73-2(free base))
|
|
98%
|
|
A-674563 is an orally available, ATP-competitive, and reversible inhibitor of Akt (Ki: 11 nM for Akt1) [1]. It exhibits inhibitory activity against PKA and Cdk2 ...
|
T3132 |
SC66
|
871361-88-5
|
98%
|
|
SC66 is a AKT inhibitor in HepG2, HA22T/VGH, and PLC/PRF/5 cells (IC50: about 0.75 μg/ml, at 72 h).
|
TN2063 |
Physalin B
|
23133-56-4
|
98%
|
|
Physalin B is one of the major active compounds from the Solanaceae family of plants and has a wide range of biological activities for the treatment of inflammat...
|
T23695 |
Akt-I-1,2
|
473382-50-2
|
98%
|
|
Akt-I-1,2 is a selective inhibitor of Akt1 and Akt2.
|
T2895 |
Lupeol
|
545-47-1
|
98%
|
|
Lupeol is a novel androgen receptor inhibitor with anti-inflammatory and antioxidant activity.
|
T6303 |
CCT128930
|
885499-61-6
|
98%
|
|
CCT128930 is a potent, ATP-competitive and selective inhibitor of Akt2 with IC50 of 6 nM, 28-fold greater selectivity for Akt2 than the closely related PKA kinas...
|
T0392 |
Artemisinin
|
63968-64-9
|
98%
|
|
Artemisinin is an ancient Chinese herbal therapy for malarial fevers which has been recently found to have potent activity against many forms of malarial organis...
|
T25017 |
AKT-I-1
|
473382-39-7
|
98%
|
|
AKT-I-1 is a selective and reversible inhibitor of Akt1.
|