Cat. No. | Product Name | Field of Application | Chemical Structure |
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DC21053 | Rivipansel sodium |
Rivipansel sodium (GMI-1070, PF-06460031) is a novel small molecule glycomimetic pan-Selectin antagonist with IC50 of 4.3 uM, 423 uM and 337 uM for E-selectin, P-selectin and L-selectin, respectively.
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DC23576 | Rislenemdaz mesylate |
Rislenemdaz (MK 0657.
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DC23619 | Rislenemdaz hydrochloride |
Rislenemdaz (MK 0657.
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DCAPI1012 | Risedronic acid (Actonel) |
Risedronic acid (Actonel)
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DC9049 | Risedronate Sodium |
Risedronate sodium is a pyridinyl biphosphonate which inhibits osteoclast-mediated bone resorption.
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DC21946 | RIPK2 inhibitor OD36 |
RIPK2 inhibitor OD36 is a potent, specific, ATP-competitive inhibitor of RIPK2 with IC50 of 5.3 nM, inhibits Tyr and Ser/Thr-directed activities of RIPK2.
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DC20536 | RIPK2 inhibitor 1 |
RIPK2 inhibitor 1 is a novel potent, selective RIPK2 inhibitor with IC50 of 5-10 nM.
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DC21945 | RIPGBM |
RIPGBM is a cell type-selective, small molecule inducer of apoptosis in GBM cancer stem cells (CSCs) with EC50 of 220 nM (GBM 1 cells).
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DC20535 | RIP1-IN-22 |
RIP1-IN-22 is a highly potent, orally available, and brain-penetrating RIP1 kinase inhibitor with pKi of 9.04.
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DCAPI1057 | Rimantadine (Flumadine) |
Rimantadine (Flumadine)
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DCAPI1446 | rifomycins |
rifomycins
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DC23909 | Rifaximin |
Rifaximin is an oral, semi-synthetic antibiotic derived from Rifamycin SV with antibacterial activity, interferes with transcription by binding to the β-subunit of bacterial RNA polymerase.
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DCAPI1283 | Rifapentine (Priftin) |
Rifapentine (Priftin)
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DC12237 | Riboflavine phosphate (Riboflavine 5'-phosphate) |
Riboflavine phosphate is a very effective NAD+-recycling agent.
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DC23186 | Rhosin |
Rhosin (G04) is a potent, specific RhoA subfamily Rho GTPases inhibitor that specifically binds to RhoA to inhibit GEF reaction of RhoA with Kd of 0.4 uM, does not interact with Cdc42 or Rac1, nor the LARG.
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DCAPI1221 | Rheochrysidin (Physcione) |
Rheochrysidin (Physcione)
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DCAPI1188 | Rhein(Monorhein) |
Rhein(Monorhein)
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DC21564 | RH01386 |
RH01386 is a small molecule that protect pancreatic β cells against endoplasmic reticulum stress-induced cell death.
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DC10191 | RG7800 |
RG7800 a small molecule SMN2 splicing modifier to enter human clinical trials to treat spinal muscular atrophy.
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DC21696 | Revexepride |
Revexepride (SSP 002358.
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DC21617 | Revaprazan hydrochloride |
Revaprazan (SB-641257.
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DC21616 | Revaprazan |
Revaprazan (SB-641257.
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DC20533 | Rev1-IN-5 |
Rev1-IN-5 is a small molecule inhibitor of the C-terminal domain of Rev1 and the Rev1-interacting region protein-protein interaction (Rev1-CT/RIR PPI) with IC50 of 2.5 uM.
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DC20532 | Retro 2 |
Retro 2 is the first small molecule inhibitor of plant toxin ricin, protects HeLa cells against Ricin, Stx1 and Stx2, selectively blocks retrograde toxin trafficking at the early endosome-TGN (trans-Golgi network) interface.
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DC20531 | Retro 1 |
Retro 1 is the first small molecule inhibitor of plant toxin ricin, protects HeLa cells against Ricin, Stx1 and Stx2, selectively blocks retrograde toxin trafficking at the early endosome-TGN (trans-Golgi network) interface.
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DC23312 | RETRA |
RETRA is a small molecule mutant p53 reactivator that activates a set of p53-regulated genes and specifically suppresses mutant p53-bearing tumor cells in vitro and in mouse xenograft.
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DC23287 | RETRA hydrochloride |
RETRA hydrochloride is a small molecule mutant p53 reactivator that activates a set of p53-regulated genes and specifically suppresses mutant p53-bearing tumor cells in vitro and in mouse xenograft.
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DC23293 | RETRA hydrobromide |
RETRA hydrobromide is a small molecule mutant p53 reactivator that activates a set of p53-regulated genes and specifically suppresses mutant p53-bearing tumor cells in vitro and in mouse xenograft.
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DC12234 | Retinyl palmitate (Vitamin A palmitate; Retinol palmitate) |
Retinyl palmitate is an ester of Retinol and is the major form of vitamin A found in the epidermis. Retinyl palmitate has been widely used in pharmaceutical and cosmetic formulations.
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DC20530 | RET-IN-23c |
RET-IN-23c is a potent and selective RET kinase inhibitor with IC50 of 61.2 nM, shows no significant inhibitory effect against VEGFR-2 and KDR.
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