产品目录
| 编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
|---|---|---|---|---|
| 20319 | Ablukast | 96566-25-5 (free acid) | 98% Min. | |
| Ablukast is a leuktriene receptor antagonist that acts as an anti-asthmatic. | ||||
| 20312 | 2-氨基-5-三氟甲基苯甲酸 | 83265-53-6 | 98% Min. |  |
| 20303 | Afabicin | 1518800-35-5 | 98% Min. |  |
| Afabicin (formerly Debio 1450, AFN-1720) is a prodrug of afabicin desphosphono, an en | ||||
| 20300 | Acoramidis (AG-10 ) | 1446711-81-4 | ≧98.0% | _1446711-81-4.png) |
| Acoramidis (formerly AG10) is an investigational, orally-administered small molecule | ||||
| 20298 | ASTX-029 | 2095719-92-7 | 98% Min. |  |
| ASTX029 is a highly potent and selective dual-mechanism ERK inhibitor. ASTX029 inhibi | ||||
| 20297 | AZD-4818 | 1003566-93-5 | 98% Min. |  |
| AZD-4818 is a chemokine CCR1 antagonist that is used for the treatment of chronic obs | ||||
| 20289 | Adavivint | 1467093-03-3 (free base) | 98% Min. | |
| 20286 | A2793 | 88349-90-0 | 98% Min. |  |
| A2793 is an inhibitor of TRESK (IC50 value of 6.8 μM for mTRESK). A2793 inhibited TW | ||||
| 20281 | ABT-384 | 868623-40-9 | ≧98.0% |  |
| ABT-384 是 11β-羟基类固醇脱氢酶 1 (HSD-1) 的有效选择性抑制剂，该 | ||||
| 20269 | AN 0128 | 872044-70-7 | 98% Min. |  |
| AN 0128, also known as CRM-0005 and ONT-0001, is a tumour necrosis factor alpha (TNF- | ||||
| 20267 | Almonertinib | 1899921-05-1 | 98% Min. |  |
| Almonertinib is an orally available inhibitor of the epidermal growth factor receptor | ||||
| 20264 | ALC-0315 | 2036272-55-4 | 98% Min. |  |
| ALC-0315 is a synthetic cationic lipid (or ionizable lipid). It is a colorless oily m | ||||
| 2105071 | AP1189 acetate | 959850-74-9 | ≧98.0% |  |
| AP1189 is a melanocortin receptor agonist on MC1 and MC3 receptors. | ||||
| 21223 | AMG-221 | 1095565-81-3 | 98% Min. |  |
| AMG-221, BVT-83370, is a potent and selective 11β-HSD1 inhibitor. AMG-221 decreased | ||||
| 20211801 | ACT-389949 (ACT389949) | 1258417-54-7 | 98% Min. | _1258417-54-7.png) |
| ACT-389949 is a potent and selective agonist of formyl peptide receptor type 2 (FPR2) | ||||
| 20111201 | AT-56 | 162640-98-4 | 98% Min. |  |
| AT-56 is a selective, competitive, and highly bioavailable inhibitor of lipocalin-typ | ||||
| 20103001 | ASN007 | 2055597-12-9 | ≧98.0% |  |
| ASN007 , a novel oral ERK inhibitor , has shown anti-tumor activity in both solid tum | ||||
| 2091501 | AB-680 | 2105904-82-1 | 98% Min. |  |
| AB-680一种是高效、可逆和选择性CD73抑制剂。AB-680是第一个临床使 | ||||
| 23948 | Apilimod mesylate ( STA-5326 ) | 870087-36-8 | ≧98.0% | _870087-36-8.png) |
| Apilimod, also known as STA-5326, is a potent IL-12/IL-23 inhibitor. Apilimod inhibit | ||||
| 2071801 | AVN-101 HCl | 1061354-48-0 | 98% |  |
| AVN-101是一种非常有效的5-HT7受体拮抗剂（Ki = 153 pM），对5-HT6、5-H | ||||
| 2071628 | APX-115 freebase | 1270084-92-8 | 98% Min. |  |
| 2071626 | Apcin | 300815-04-7 | 98% Min. |  |
| Apcin is an inhibitor of the anaphase-promoting complex/cyclosome (APC/C). It acts by | ||||
| 2071552 | Astemizole | 68844-77-9 | 98% Min. |  |
| Astemizole is a histamine H1-receptor antagonist. Astemizole competitively binds to h | ||||
| 2071539 | ARV-771 | 1949837-12-0 | 98% Min. |  |
| ARV-771 is a small-molecule pan-BET degrader. ARV-771 demonstrates dramatically impro | ||||
| 2071531 | AZD-7648 | 2230820-11-6 | 98% Min. |  |
| AZD-7648 is a potent and selective DNA-PK inhibitor. | ||||
| 2071530 | AWZ1066S | 239272-16-1 | 98% Min. |  |
| AWZ1066S is a highly specific anti-Wolbachia drug candidate for a short-course treatm | ||||
| 2071523 | AER-271 | 634913-39-6 | 98% Min. |  |
| AER-271 is a potent aquaporin-4 (AQP4) inhibitor. AER-271 blocks acute cerebral edema | ||||
| 2071517 | ABX-1431 | 1446817-84-0 | 98% Min. |  |
| ABX-1431 is a covalent, irreversible MGLL inhibitor. ABX-1431 is currently entering c | ||||
| 2071508 | AZ31 | 2088113-98-6 | 98% Min. |  |
| AZ31 is a potent and highly selective ATM inhibitor. | ||||
| 2071503 | AB-423 | 1572510-80-5 | 98% Min. |  |
| AB-423 is a novel inhibitor of hepatitis b virus pregenomic rna encapsidation | ||||