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ADH-503;ADH503;ADH 503

ADH-503;ADH503;ADH 503

中文名稱ADH-503;ADH503;ADH 503
中文同義詞(Z)-4-[5-(3-芐基-2,4-二氧代噻唑烷-5-亞甲基)-呋喃-2-基]-苯甲酸 (2-羥基-乙基)-三甲基銨鹽;LEUKADHERIN-1 CHOLINE SALT;化合物ADH-503;ADH-503(鎓鹽);2-羥基-N,N,N-三甲基乙烷-1-氨基鎓(Z)-4-(5-((3-芐基-4-氧代-2-硫代噻唑烷-5-亞基)甲基)呋喃-2-基)苯甲酸鹽;化合物ADH-503,10 MM DMSO 溶液
英文名稱ADH-503
英文同義詞ADH 503;ADH503;ADH-503;ADH-503;ADH503;ADH 503;ADH-503 - Leukadherin-1 choline salt;ADH-503 [(Z)-Leukadherin-1 choline;2-Hydroxy-N,N,N-trimethylethan-1-aminium (Z)-4-(5-((3-benzyl-4-oxo-2-thioxothiazolidin-5-ylidene)methyl)furan-2-yl)benzoate;tumor-infiltrating,CD11b,ADH-503,Inhibitor,tumorassociated,dendritic,immunosuppressive,macrophages,repolarization,allosteric,inhibit,Complement System,ADH503,orally,ADH 503
CAS號2055362-74-6
分子式C27H29N2O5S2+
分子量525.66
EINECS號
相關(guān)類別制劑-激動劑
Mol文件2055362-74-6.mol
結(jié)構(gòu)式ADH-503;ADH503;ADH 503 結(jié)構(gòu)式

ADH-503;ADH503;ADH 503 性質(zhì)

儲存條件Store at -20°C
溶解度二甲基亞砜:21.43 mg/mL(40.85 mM)
形態(tài)固體
顏色棕至紅棕色

ADH-503;ADH503;ADH 503 用途與合成方法

ADH-503 ((Z)-Leukadherin-1 choline) 是一種具有口服活性的,變構(gòu)的 CD11b 激動劑。ADH-503 可以導(dǎo)致與腫瘤相關(guān)的巨噬細(xì)胞重新極化,減少腫瘤浸潤性免疫抑制骨髓細(xì)胞的數(shù)量,并增強(qiáng)樹突狀細(xì)胞的反應(yīng)。

CD11b

ADH-503 ((Z)-Leukadherin-1 choline; 4 μM; 8 days) reduces the numbers of total tumor-infiltrating CD11b + cells and subsets of CD11b + monocytes, granulocytes, eosinophils, and macrophages.

ADH-503 ((Z)-Leukadherin-1 choline; oral gavage; 30, 60, or 120 mg/kg; twice a day for 60 days) delayes tumor progression, leading to a significantly decreased tumor burden in time-point analysis and improved overall survival.
ADH-503 (oral gavage; 30, 100 mg/kg; twice a day; on days 1 and 5) has the mean half-life of 4.68 and 3.95 hours, a maximum concentration of 1716 and 2594 ng/mL and AUC 0-t in the plasma of 6950 and 13962 ng.h/mL at 30 and 100 mg/kg dosing, respectively.

Animal Model: KPC mice [p48-CRE/Lox-stop-Lox(LSL)-Kras G12D /p53 flox/flox ]
Dosage: 30, 60, or 120 mg/kg
Administration: Oral gavage; 60 days
Result: Delayed tumor progression, leading to a significantly decreased tumor burden in time-point analysis and improved overall survival.
Animal Model: Male rats
Dosage: 30, 100 mg/kg (Pharmacokinetic Analysis)
Administration: Oral gavage twice a day; on days 1 and 5
Result: Had the mean half-life of 4.68 and 3.95 hours, a maximum concentration of 1716 and 2594 ng/mL and AUC 0-t in the plasma of 6950 and 13962 ng.h/mL at 30 and 100 mg/kg dosing, respectively.

安全信息

MSDS信息

更新日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價(jià)格
2025/02/08HY-15701BADH-503;ADH503;ADH 503
ADH-503
2055362-74-65mg550元
2025/02/08HY-15701BADH-503;ADH503;ADH 503
ADH-503
2055362-74-610mM * 1mLin DMSO635元

ADH-503;ADH503;ADH 503 上下游產(chǎn)品信息

"ADH-503;ADH503;ADH 503"相關(guān)產(chǎn)品信息
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