| R2030102 |
Tamoxifen (ICI 47699; (Z)-Tamoxifen; trans-Tamoxifen) |
Tamoxifen (ICI 47699) is a selective estrogen receptor modulator (SERM) which bl
|
| R2030103 |
SRT2183 |
SRT 2183 is a selective Sirtuin-1 (SIRT1) activator with an EC1.5 value of 0.36
|
| R2030104 |
SRT3025 |
SRT3025 is an orally available small molecule activator of the SIRT1 e
|
| R2030105 |
Caerulomycin A (Cerulomycin; Caerulomycin) |
Caerulomycin A (Cerulomycin; Caerulomycin), an antifungal compound, induces gene
|
| R2030106 |
TAK960 |
TAK-960 is an orally available, selective inhibitor of polo-like kinase 1 (PLK1)
|
| R2030108 |
IR820 |
|
| R2030109 |
FD-1080 |
|
| R2030110 |
Cardiogreen (Foxgreen; IC Green; Indocyanine green) |
Cardiogreen is a low toxicic fluorescent agent that has been widely used in medi
|
| R2030111 |
IR-1048 Tetrafluoroborate |
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| R2030113 |
Imidazole ketone erastin (IKE) |
Imidazole ketone erastin (IKE) is a potent, selective, and metabolically stable
|
| R2030114 |
L-779450 |
L-779450 is a potent and selective B-Raf kinase inhibitor with a Kd of 2.4 nM.&n
|
| R2030116 |
TAK-981;TAK981 |
TAK-981 is a first in class and selective inhibitor of the SUMOylation enzymatic
|
| R2030117 |
AZ505 |
AZ505 is a potent and selective SMYD2 inhibitor with IC50 of 0.12 μM.
|
| R2030118 |
BAY-598 |
BAY-598 is selective small molecule inhibitor of SMYD2 with an IC50 of 27 nM.
|
| R2030119 |
CTEP (RO 4956371; mGluR5 inhibitor) |
CTEP (RO 4956371) is a novel, long-acting, orally bioavailable allosteric antago
|
| R2030120 |
Basimglurant (RG7090; CTEP Derivative) |
Basimglurant (RG7090) is a potent, selective and orally available mGlu5 negative
|
| R2030121 |
D-Luciferin |
D-luciferin is the natural substrate of luciferases that catalyze the production
|
| R2030124 |
LDN-192960 |
LDN-192960 is an inhibitor of Haspin and Dual-specificity Tyrosine-regulated Kin
|
| R2030125 |
Motesanib Diphosphate (AMG-706) VM-2005 |
Motesanib Diphosphate (AMG 706 Diphosphate) is a potent ATP-competitive inhibito
|
| R2030126 |
PTC-209 |
PTC-209 is a specific BMI-1 inhibitor with an IC50 of 0.5 μM.
|
| R2030127 |
SMI-4a |
(Z)-SMI-4a is a poten, selective, cell-permeable and ATP-competitive Pim-1 inhib
|
| R2030128 |
SU-9516 |
SU9516 is a potent CDK2 inhibitor, with an IC50 of 22 nM, and also shows inhibit
|
| R2030129 |
TDZD-8 (GSK-3β Inhibitor I; NP 01139) |
TDZD-8 is an inhibitor of GSK-3β, with an IC50 of 2 μM; TDZD-8 shows less potent
|
| R2030130 |
UNC-669 |
UNC 669 is a potent antagonist of L3MBTL1(IC50=4.2 uM) and L3MBTL3(IC50=3.1 uM).
|
| R2030131 |
WZ-811 |
WZ811 is an orally active, highly potent competitive antagonist of CXCR4. WZ811
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