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| Cat.No. | Product name | Product Description |
| R202337 | AM-0902;AM0902 | AM-0902 is a potent, selective transient receptor potential A1 (TRPA1) antagonis |
| R202338 | MD2-IN-1 | MD2-IN-1 is an inhibitor of Myeloid differentiation protein 2 (MD2) with a KD of |
| R202339 | LYN-1604;LYN1604 | LYN-1604 is a potent UNC-51-like kinase 1 (ULK1) agonist with an EC50 of 18.94 n |
| R202340 | LYN-1604 hydrochloride | LYN-1604 hydrochloride is a potent ULK1 activator with an EC50 of 18.94 nM. |
| R202341 | Letermovir;AIC246 | Letermovir is a novel inhibitor of CMV, which targets the viral terminase comple |
| R202342 | Dyngo-4a | Dyngo-4a is a potent dynamin inhibitor with IC50 of 0.38 μM, |
| R202343 | iCRT3 | iCRT3 is an inhibitor of both Wnt and β-catenin-responsive transcription. |
| R202344 | Tyrphostin AG 528 (Synonyms: Tyrphostin B66; AG 528) | Tyrphostin AG 528 is an inhibitor of EGFR and ErbB2 with IC50s of 4.9 and 2.1 μM |
| R202346 | 2H-Indol-2-one,3-[(3,5-dibromo-4-hydroxyphenyl)methylene]-1,3-dihydro-5-iodo- | GW 5074 is a potent and selective c-Raf inhibitor with IC50 of 9 nM, and has no |
| R202347 | SB-366791;SB366791 | SB-366791 is a potent , competitive and selective vanilloid receptor (VR1/TRPV1) |
| R202348 | KN-93 hydrochloride;KN93 hydrochloride | KN-93 hydrochloride is a cell-permeable, reversible and competitive inhibitor ca |
| R202349 | KN92 | KN-92 is an inactive derivative of KN-93. KN-93 is a selective inhibitor of Ca2+ |
| R202350 | H-89 dihydrochloride (Protein kinase inhibitor H-89 dihydrochloride) | H-89 dihydrochloride is a potent and selective inhibitor of protein kinase A (PK |
| R202351 | KN-93 (phosphate) | KN-93 phosphate is a novel membrane-permeant synthetic inhibitor of purified neu |
| R202401 | Larotrectinib (Synonyms: LOXO-101; ARRY-470) | Larotrectinib (LOXO-101) is an ATP-competitive oral, selective inhibitor of the |
| R202402 | PFK-158;;PFK158 | PFK-158 is a potent and selective inhibitor of PFKFB3 that is currently being in |
| R202403 | AS1517499 | AS1517499 is a potent STAT6 inhibitor with an IC50 of 21 nM. |
| R202404 | PD173955 | PD173955 is src family-selective tyrosine kinase inhibitor with IC50 of ~22 nM f |
| R202405 | PF-03463275;PF03463275 | CAS NO.：1366657-90-0Product Name：PF-03463275;PF03463275Synonyms：EINECS:Molecular |
| R2030372 | DBCO-PEG4-SE | DBCO-PEG4-NHS ester is a PEG-based PROTAC linker that can be used in the synthes |
| R2003041 | LIT-001 TFA | LIT-001 is the first nonpeptide oxytocin receptor (OT-R) agonist (EC50=55 nM; Ki |
| R2003051 | Cefminox sodium (MT-141) | Cefminox sodium (MT-141) is a semisynthetic cephamycin, which exhibits a broad s |
| R2003081 | SRT3025 HCl;Sirtuin modulator 1 | Sirtuin modulator 1 is a modulator of SIRTl, a homolog of SIRT3, with EC1.5 of & |
| R00311 | Cardiogenol C, Hydrochloride | Cardiogenol C hydrochloride is a cell-permeable pyrimidine compound which potent |
| R00313 | Cisplatin (CDDP; cis-Diaminodichloroplatinum) | Cisplatin is a antineoplastic chemotherapy drug which works by cross-linking wit |
