Cat. No. | Product name | CAS No. |
DC9383 |
Rimonabant (Hydrochloride)
Featured
Rimonabant Hcl(SR141716A) is a selective central cannabinoid (CB1) receptor inverse agonist with Ki of 1.8 nM. |
158681-13-1 |
DC8876 |
Rimonabant(SR141716)
Featured
Rimonabant(SR141716) is a selective central cannabinoid (CB1) receptor inverse agonist with Ki of 1.8 nM. |
168273-06-1 |
DC20535 |
RIP1-IN-22
RIP1-IN-22 is a highly potent, orally available, and brain-penetrating RIP1 kinase inhibitor with pKi of 9.04. |
2095515-38-9 |
DC10389 |
RIPA-56
Featured
RIPA-56 is a highly potent, selective, and metabolically stable inhibitor of receptor-interacting protein 1 (RIP1) with an IC50 of 13 nM. |
1956370-21-0 |
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). |
355406-76-7 |
DC20536 |
RIPK2 inhibitor 1
RIPK2 inhibitor 1 is a novel potent, selective RIPK2 inhibitor with IC50 of 5-10 nM. |
1290490-78-6 |
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. |
1638644-62-8 |
DC21563 |
Risdiplam
Featured
Risdiplam (RG7916, RG-7916, RO7034067) is a highly potent, selective, orally active SMN2 splicing modifier for treatment of spinal muscular atrophy (SMA). |
1825352-65-5 |
DC23619 |
Rislenemdaz hydrochloride
Rislenemdaz (MK 0657. |
808733-06-4 |
DC23576 |
Rislenemdaz mesylate
Rislenemdaz (MK 0657. |
1893392-76-1 |
DC7268 |
Risperidone(R 64 766)
Risperidone(R 64 766) is a serotonin 5-HT2 receptor blocker(Ki= 0.16 nM) and a potent dopamine D2 receptor antagonist(Ki= 1.4 nM). |
106266-06-2 |
DC9475 |
Ritonavir
Featured
Ritonavir is an inhibitor of HIV protease used to treat HIV infection and AIDS,showed potent activity against COVID-19(SARS-COV-2) . |
155213-67-5 |
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. |
1189037-60-2 |
DC23185 |
RJR-2403 oxalate
RJR-2403 (Rivanicline, Metanicotine) is a potent, selective neuronal nicotinic ACh (nAChR) agonist with high affinity to rat brain cortex (Ki=26 nM), does not significantly activate muscle type nAChRs or muscarinic receptors. |
220662-95-3 |
DC23197 |
RJR-2403
RJR-2403 (Rivanicline, Metanicotine) is a potent, selective neuronal nicotinic ACh (nAChR) agonist with high affinity to rat brain cortex (Ki=26 nM), does not significantly activate muscle type nAChRs or muscarinic receptors. |
15585-43-0 |
DC12481 |
RK-20449
RK-20449 (RK20449) is a potent, small molecule inhibitor of hematopoietic cell kinase (HCK) with IC50 of 0.43 nM. |
364042-47-7 |
DC11325 |
RN-1734
Featured
RN-1734 is a transient receptor potential vanilloid 4 (TRPV4) antagonist, blocking calcium influx induced by the TRPV4 agonist 4α-phorbol 12,13-didecanoate with IC50 values of 2.3, 5.9, and 3.2 µM for human, mouse, and rat TRPV4, respectively. |
946387-07-1 |
DC23023 |
RNase L-IN-2
RNase L-IN-2 is a small-molecule activator of RNase L with EC50 of 22 uM. |
357618-26-9 |
DC22638 |
RNPA1000
RNPA1000 is a potent, specific small molecule inhibitor of S. aureus RnpA RNA degradation activity (IC50=100-125 uM), limits S. aureus mRNA turnover and growth. |
359600-10-5 |
DC21569 |
RNPA2000
RNPA2000 is a small-molecule inhibitor of Staphylococcus aureus RnpA-mediated RNA turnover and tRNA processing (IC50=130 uM). |
329214-04-2 |
DC23852 |
Ro 08-2750
Ro 08-2750 (Ro 082750) is a potent, selective, non-peptide nerve growth factor (NGF) inhibitor that binds to NGF dimer with Kd of 1 uM. |
37854-59-4 |
DC23321 |
RO 2443
RO 2443 is a potent, dual MDM2/MDMX antagonist that inhibits both MDM2 (IC50=33 nM) and MDMX (IC50=41 nM) binding to p53, but poor water solubility does not allow for a meaningful assessment of its cellular activity.. |
1416663-79-0 |