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| Catalog | name | Description | price |
|---|---|---|---|
| R-C-3008 | Ozogamicin CAS:400046-53-9 | Ozogamicin is an antibody-drug conjugate Linker.Only for scientific research, not for human body. | price> |
| R-R-4678 | DHODH-IN-16 CAS No.2511248-11-4 | DHODH-IN-16/CAS No.2511248-11-4 is a potent dihydroorotate dehydrogenase (DHODH) inhibitor with an IC50 of 0.396 nM for human DHODH. | price> |
| R-C-2979 | BAY-707 CAS:2109805-96-9 | Bay-707 is a substrate competitive, efficient and selective inhibitor of MTH1 (NUDT1), with an IC50 value of 2.3 nm. Bay-707 has good pharmacokinetic characteristics compared with other MTH1 compounds and has good tolerance in mice, but the experiment obviously lacks anticancer effect in vitro or in vivo.Only for scientific research, not for human body. | price> |
| R-C-3009 | Etanercept CAS: 185243-69-0 | Etanercept,a dimeric fusion protein that binds TNF, acts as a TNF inhibitor.Only for scientific research, not for human body. | price> |
| R-R-4679 | Ibezapolstat CAS No.1275582-97-2 | Ibezapolstat (ACX-362E)/CAS No.1275582-97-2 is a first-in-class, orally active DNA polymerase IIIC (pol IIIC) inhibitor, with a Ki of 0.325 μM for the DNA pol IIIC from C. difficile. Ibezapolstat is developed for the research of C. difficile infection(CDI). | price> |
| R-C-2980 | Levosulpiride CAS:23672-07-3 | Levosulpiride (rv-12309) is the (s) enantiomer of sulpiride and a dopamine D2 receptor antagonist.Only for scientific research, not for human body. | price> |
| R-C-3011 | IACS-13909 CAS :2160546-07-4 | IACS-13909 is a selective, potent and orally active SHP2 allosteric inhibitor with an IC50 of 15.7 nM and a Kd of 32 nM. | price> |
| R-R-4680 | Deoxycytidine triphosphate trisodium salt CAS No.109909-44-6 | Deoxycytidine triphosphate trisodium salt (dCTP trisodium salt)/CAS No.109909-44-6 is a nucleoside triphosphate that can be used for DNA synthesis. Deoxycytidine triphosphate trisodium salt has many applications, such as real-time PCR, cDNA synthesis, and DNA sequencing. | price> |
| R-C-2981 | Mianserin CAS:24219-97-4 | Mianserin is an H1 receptor Reverse agonist.Only for scientific research, not for human body. | price> |
| R-R-4681 | N-Acetyl-Calicheamicin CAS No.108212-76-6 | N-Acetyl-Calicheamicin (N-Acetyl-Calicheamicin γ)/CAS No.108212-76-6, an enediyne anti-tumor antibiotic, is an ADC cytotoxin. N-Acetyl-Calicheamicin can induce DNA damage, and can be used in the synthesis of ADC. | price> |
| R-C-2982 | LED209 CAS:245342-14-7 | Led209 is an effective small molecule inhibitor of bacterial receptor qseC. It is an effective prodrug with high selectivity for qseC. Only for scientific research, not for human body. | price> |
| R-C-3012 | WUN-29654 (CRBN modulator-1) CAS:2407829-65-4 | WUN-29654 (CRBN modulator-1, compound 10) is a Thalidomide analog and a CRBN modulator with IC50 of 3.5 μM and Ki of 0.98 μM for CRBN binding. | price> |
| R-R-4682 | Garenoxacin Mesylate hydrate CAS No.223652-90-2 | Garenoxacin (BMS284756) Mesylate hydrate/CAS No.223652-90-2 is an orally active quinolone antibiotic and has a broad spectrum of activity against a wide array of gram-positive and gram-negative bacteria, anaerobes, and fastidious organisms. | price> |
| R-C-2983 | Ro 64-5229 CAS: 139339-45-0 | Ro24-7429 is an effective and orally active HIV-1 transactivator Tat antagonist. Ro24-7429 is also a Runx1 inhibitor. Only for scientific research, not for human body. | price> |
| R-C-3013 | ML-385 CAS:846557-71-9 | ML385 inihbits the activity of the Nrf2 transcription factor by binding to Neh1, a CNC-bZIP domain that allows Nrf2 to heterodimerize with small Maf proteins, blocking NRF2 transcriptional activity. Only for scientific research, not for human body. | price> |
| R-R-4683 | Netropsin dihydrochloride CAS No.18133-22-7 | Netropsin dihydrochloride/CAS No.18133-22-7 is a small-molecule MGB (minor-groove binder), inhibits the catalytic activity of isolated topoisomerase and interferes with the stabilization of the cleavable complexes of topoisomerase II and I in nuclei. Netropsin dihydrochloride exhibits antiviral activity against the vaccinia virus. | price> |
| R-C-3014 | SB525334 CAS:356559-20-1 | SB525334 is a potent and selective inhibitor of TGFβ receptor I (ALK5) with IC50 of 14.3 nM in a cell-free assay, 4-fold less potent to ALK4 than ALK5 and inactive to ALK2, 3, and 6.Only for scientific research, not for human body. | price> |
| R-R-4684 | Adenine-13C CAS No.86967-48-8 | Adenine-13C/CAS No.86967-48-8 is the 13C labeled Adenine. Adenine (6-Aminopurine), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine acts as a chemical component of DNA and RNA. Adenine also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis. | price> |
| R-C-3015 | Frentizole CAS:26130-02-9 | Frentizole (Frentizol) is a novel inhibitor of amyloid beta peptide (Abeta) binding alcohol dehydrogenase (ABAD) interaction with IC50 of 200 μM. Only for scientific research, not for human body. | price> |
| R-R-4685 | Tezacitabine CAS No.130306-02-4 | Tezacitabine/CAS No.130306-02-4 is a cytostatic and cytotoxic antimetabolite and a nucleoside analogue. Tezacitabine irreversibly inhibits the ribonucleotide reductase and interferes with DNA replication and repair. Tezacitabine effectively induces cells apoptotic. Tezacitabine has the potential for leukemias and solid tumors (carcinomas) treatment. | price> |

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