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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T19837 | O4 | O 4,O-4 | |
O4 is a novel stabilizer of amyloid- fibrils. O4 used for accelerating the formation of end-stage mature fibrils. | |||
T67275 | Bis[2-(1-isoquinolinyl-N)phenyl-C](2,4-pentanedionato-O2,O4)iridium(III) | ||
Bis[2-(1-isoquinolinyl-N)phenyl-C](2,4-pentanedionato-O2,O4)iridium(III) is a useful organic compound for research related to life sciences. The catalog number is T67275 and the CAS number is 435294-03-4. | |||
T22416 | RO495 | CS-2667 | Tyrosine Kinases , JAK |
RO495 (CS-2667), a potent inhibitor of TYK2, inhibits TYK2 with IC50 of 1.5nM as tested in cell-based pharmacological assays | |||
T2437 | O4I2 | O-4I2,O4I2 | OCT |
O4I2 is an effective Oct3/4 inducer in various human cell lines including human fibroblasts. | |||
TP2481 | FOXO4-DRI acetate | Others | |
FOXO4-DRI acetate is a bioactive chemical. | |||
T77578 | CHBO4 | MAO , ROS | |
CHBO4 is an hMAO-B inhibitor that is potent, reversible, competitive and selective.The IC50 value of CHBO4 against hMAO-B in the CHBO assay was 0.031 μM, and the Ki value was 0.010 ± 0.005 μM.CHBO4 reduces cellular damag... | |||
T5412 | RO4987655 | CH4987655,RG7167 | MEK |
RO4987655 (RG7167) is an orally active and highly selective MEK inhibitor (IC50: 5.2 nM for MEK1/MEK2). | |||
T2439 | O4I1 | OCT | |
O4I1 is an effective Oct3/4 inducer. | |||
T6274 | RO4929097 | RG-4733 | Beta Amyloid , Gamma-secretase |
RO4929097 (RG-4733), a γ secretase inhibitor (IC50: 4 nM), inhibits cellular processing of Aβ40 and Notch (EC50: 14/5 nM). | |||
T74186 | PROTAC-O4I2 | Apoptosis , PROTACs | |
PROTAC-O4I2, a PROTAC ligand targeting splicing factor 3B1 (SF3B1), induced FLAG-SF3B1 degradation in K562 cells with an IC50 value of 0.244 μM. PROTAC-O4I2 induced apoptosis in K562 WT cells. | |||
T82654 | Cy3-PEG3-TCO4 | ||
Cy3-PEG3-TCO4, a dye derivative with three polyethylene glycol (PEG) units linked to Cyanine 3 (Cy3), possesses a trans-cyclooctene (TCO) group capable of undergoing the inverse electron demand Diels-Alder reaction (iEDD... | |||
T66985 | TAK 438 xC4H4O4 | ||
TAK 438 xC4H4O4 is a useful organic compound for research related to life sciences and the catalog number is T66985. | |||
T76563 | FOXO4-DRI | ||
FOXO4-DRI, a cell-permeable peptide antagonist, inhibits the interaction between FOXO4 and p53. It functions as a senolytic peptide, promoting apoptosis in senescent cells [1]. | |||
T83495 | [D-Pro4,D-Trp7,9] Substance P (4-11) | ||
[D-Pro4,D-Trp7,9] Substance P (4-11) acts as a potent antagonist to Substance P, significantly reducing plasma aldosterone (ALDO) concentrations[1]. | |||
T82656 | Cy3-PEG2-TCO4 | ||
Cy3-PEG2-TCO4, a Cyanine 3 (Cy3) dye derivative with two polyethylene glycol (PEG) units, utilizes its TCO moiety to engage in inverse electron demand Diels-Alder reactions (iEDDA) with Tetrazine-functionalized molecules... | |||
T83496 | [D-Pro4,D-Trp7,9,10] Substance P (4-11) | ||
[D-Pro4,D-Trp7,9,10] Substance P (4-11) serves as a potent antagonist of the tachykinin family of neuropeptides [1]. | |||
T82943 | AtPCO4-IN-1 | ||
AtPCO4-IN-1 is a selective AtPCO4 inhibitor, exhibiting an IC50 value of 264.4 μM [1]. | |||
T76406 | [D-Pro4,D-Trp7,9,Nle11] Substance P (4-11) | ||
[D-Pro4,D-Trp7,9,Nle11] Substance P (4-11) is a potent neurokinin NK1 antagonist that effectively inhibits the actions of gold-protein-substance P (GPSP) and substance P (SP), demonstrating its efficacy in neutralizing t... | |||
T28600 | Ro4491533 | Ro 4491533,Ro-4491533 | |
Ro4491533 is a potent and selective negative allosteric modulator for group II of the metabotropic glutamate receptors (mGluR2/3). | |||
T28601 | RO4988546 | RO-4988546,RO 4988546 | |
RO4988546 is a potent negative allosteric modulator of mGlu₂/₃. |