Catalog |
name |
Description |
price |
R-R-4593 |
BAY-2402234 CAS No.2225819-06-5 |
BAY-2402234/CAS No.2225819-06-5 is a selective dihydroorotate dehydrogenase (DHODH) inhibitor for the treatment of myeloid malignancies. |
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R-R-4595 |
NSC 617145 CAS No.203115-63-3 |
NSC 617145/CAS No.203115-63-3 is a selective werner syndrome helicase (WRN) helicase inhibitor with an IC50 value of 230 nM. NSC 617145 inhibits WRN ATPase, and induces double-strand breaks (DSB) and chromosomal abnormalities. NSC 617145 shows selective for WRN over BLM, FANCJ, ChlR1, RecQ, and UvrD helicases. |
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R-R-4596 |
IMP-1088 CAS No.2059148-82-0 |
IMP-1088/CAS No.2059148-82-0 is a potent human N-myristoyltransferases NMT1 and NMT2 dual inhibitor with IC50s of <1 nM for HsNMT1 and HsNMT2. IMP-1088 has a Kd of <210 pM for HsNMT1. IMP-1088 efficiently blocks rhinovirus replication by blocking rhinovirus virus-encoded protein (VP0) N-myristoylation. IMP-1088 protects host cells from the cytotoxic effects of viral infection. |
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R-R-4597 |
CX-5461 dihydrochloride |
CX-5461 dihydrochloride is a potent and orally bioavailable inhibitor of Pol I-mediated rRNA synthesis, with IC50s of 142 nM in HCT-116, 113 nM in A375, and 54 nM in MIA PaCa-2 cells, and shows little or no effect on Pol II (IC50 ≥25 μM). |
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R-R-4598 |
Tirapazamine CAS No.27314-97-2 |
Tirapazamine (SR259075)/CAS No.27314-97-2 is an anticancer agent that shows selective cytotoxicity for hypoxic cells in solid tumors, thereby inducing single-and double-strand breaks in DNA, base damage, and cell death. Tirapazamine is an anticancer and bioreductive agent.Tirapazamine (SR259075) can enhance the cytotoxic effects of ionizing radiation in hypoxic cells. |
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R-R-4599 |
RP-6685 CAS No.2832047-80-8 |
RP-6685/CAS No.2832047-80-8 is a potent, selective and orally active DNA polymerase theta (Polθ) inhibitor with an IC50 value of 5.8 nM (PicoGreen assay). RP-6685 shows antitumor efficacy in mouse tumor xenograft model. RP-6685 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. |
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R-R-4600 |
D-I03 CAS No.688342-78-1 |
D-I03/CAS No.688342-78-1 is a selective RAD52 inhibitor with a Kd of 25.8 µM. D-I03 specifically inhibits RAD52-dependent single-strand annealing (SSA) and D-loop formation with IC50s of 5 µM and 8 µM, respectively. D-I03 suppresses growth of BRCA1- and BRCA2-deficient cells and inhibits formation of damage-induced RAD52 foci, but does not effect on RAD51 foci induced by Cisplatin. |
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R-R-4601 |
Quarfloxin CAS No.865311-47-3 |
Quarfloxin (CX-3543)/CAS No.865311-47-3, a fluoroquinolone derivative with antineoplastic activity, targets and inhibits RNA pol I activity, with IC50 values in the nanomolar range in neuroblastoma cells. Quarfloxin disrupts the interaction between the nucleolin protein and a G-quadruplex DNA structure in the ribosomal DNA (rDNA) template. |
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R-R-4602 |
Nusinersen CAS No.1258984-36-9 |
Nusinersen/CAS No.1258984-36-9 is an antisense oligonucleotide agent that modifies pre–messenger RNA splicing of the SMN2 gene and thus promotes increased production of full-length SMN protein.The free form of the compound is prone to instability, it is advisable to consider the stable salt form (Nusinersen sodium) that retains the same biological activity. |
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R-R-4603 |
GS-443902 trisodium CAS No.1355050-21-3 |
GS-443902 trisodium (GS-441524 triphosphate trisodium)/CAS No.1355050-21-3 is a potent viral RNA-dependent RNA-polymerases (RdRp) inhibitor with IC50s of 1.1 µM, 5 µM for RSV RdRp and HCV RdRp, respectively. GS-443902 trisodium is the active triphosphate metabolite of Remdesivir (GS-5734). |
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