T2220 |
2-Methoxyestradiol
|
362-07-2
|
99.95%
|
|
2-Methoxyestradiol (2-ME2) is an orally bioavailable estradiol metabolite with potential antineoplastic activity. 2-Methoxyestradiol inhibits angiogenesis by red...
|
T1569 |
Tigecycline
|
220620-09-7
|
99.94%
|
|
Tigecycline (GAR-936) is a broad-spectrum glycylcycline antibiotic derived from tetracycline. Tigecycline binds to the 30S ribosomal subunit, thereby interfering...
|
T2355 |
CFTR(inh)-172
|
307510-92-5
|
99.94%
|
|
CFTR(inh)-172 (CFTR Inhibitor-172) is a voltage-independent, selective CFTR inhibitor.
|
T1535 |
Sodium 4-phenylbutyrate
|
1716-12-7
|
99.94%
|
|
Sodium 4-phenylbutyrate (TriButyrate), a transcriptional regulator, reversibly inhibits class I and II histone deacetylases (HDACs )resulting in a global increas...
|
T2492 |
Perifosine
|
157716-52-4
|
99.94%
|
|
Perifosine (KRX-0401) is an oral-active, alkyl-phosphocholine Akt inhibitor with potential antineoplastic activity.
|
T17209 |
UVI 3003
|
847239-17-2
|
99.94%
|
|
UVI 3003 is a highly selective antagonist of the retinoid X receptor. UVI 3003 inhibits Xenopus and human RXRα in Cos7 cells (IC50s: 0.22 and 0.24 μM, respective...
|
T6151 |
GW 501516
|
317318-70-0
|
99.94%
|
|
GW 501516 (Endurobol) is a effective and highly specifc PPARβ/δ agonist (EC50: 1 nM), with 1000-fold selectivity over hPPARα/γ.
|
T1969 |
DBEQ
|
177355-84-9
|
99.94%
|
|
DBEQ (JRF 12) is a selective, potent, reversible, and ATP-competitive p97 inhibitor.
|
T4645 |
TA-01
|
1784751-18-3
|
99.94%
|
|
TA-01 is a potent CK1 and p38 MAPK inhibitor, with IC50s of 6.4 nM, 6.8 nM, 6.7 nM for CK1ε, CK1δ and p38 MAPK, respectively.
|
T2233 |
GW 4064
|
278779-30-9
|
99.94%
|
|
GW 4064 is an effective farnesoid X receptor (FXR) agonist (EC50 =65 nM).
|
T1105 |
Penfluridol
|
26864-56-2
|
99.94%
|
|
Penfluridol (TLP-607) is a highly potent antipsychotic.
|
T4S2126 |
Ginkgetin
|
481-46-9
|
99.94%
|
|
1. Ginkgetin has anti-influenza virus and anti-fungal activities. 2. Ginkgetin has anti-inflammatory activity, can down-regulates COX-2 induction in vivo against...
|
T6167 |
SU9516
|
377090-84-1
|
99.94%
|
|
SU9516 is a potent CDK2 inhibitor, with an IC50 of 22 nM, and also has inhibitory effects on CDK1 and CDK4, with IC50s of 40 nM and 200 nM, respectively.
|
T0010 |
6-Mercaptopurine
|
50-44-2
|
99.94%
|
|
6-Mercaptopurine (6-MP) is an antimetabolite antineoplastic agent with immunosuppressant properties. It interferes with nucleic acid synthesis by inhibiting puri...
|
T2829 |
Isoalantolactone
|
470-17-7
|
99.94%
|
|
Isoalantolactone (Isohelenin), isolated from Inula spp., can inhibit the growth of several types of Y cells.
|
T3843 |
Pinosylvin
|
22139-77-1
|
99.93%
|
|
Pinosylvin (5-Styrylresorcinol) induces autophagy via AMPK activation. Pinosylvin is likely to act as a pro-angiogenic factor.
|
T1583 |
Vorinostat
|
149647-78-9
|
99.93%
|
|
Vorinostat (SAHA) is a pan-histone deacetylase (HDAC) inhibitor (IC50=10 nM) with inhibitory activity against HDAC1/2/3/6/7/11. Vorinostat has antitumor activity...
|
T0132 |
Etoposide
|
33419-42-0
|
99.93%
|
|
Etoposide (VP-16-213) is a topoisomerase II inhibitor that inhibits DNA synthesis by forming a complex with topoisomerase II and DNA (IC50=60.3 μM). Etoposide ha...
|
T0164 |
Oxaliplatin
|
61825-94-3
|
99.93%
|
|
Oxaliplatin (L-OHP) is a DNA alkylating agent, an inhibitor of DNA synthesis. Oxaliplatin causes DNA cross-linking damage, preventing DNA replication and transcr...
|
T2202 |
Lithocholic acid
|
434-13-9
|
99.93%
|
|
Lithocholic acid (3α-Hydroxy-5β-cholanic acid) is a bile acid formed from chenodeoxycholate by bacterial action, usually conjugated with glycine or taurine. It a...
|