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2055362-74-6

中文名稱(chēng) ADH-503;ADH503;ADH 503
英文名稱(chēng) ADH-503
CAS 2055362-74-6
分子式 C27H29N2O5S2+
分子量 525.66
MOL 文件 2055362-74-6.mol
更新日期 2024/12/15 19:35:20
2055362-74-6 結(jié)構(gòu)式 2055362-74-6 結(jié)構(gòu)式

基本信息

中文別名
(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
英文別名
ADH503
ADH 503
ADH-503
ADH-503
ADH503
ADH 503
ADH-503 - Leukadherin-1 choline salt

物理化學(xué)性質(zhì)

儲(chǔ)存條件-20°C儲(chǔ)存
溶解度DMSO: 21.43 mg/mL (40.85 mM)
形態(tài)Solid
顏色Brown to reddish brown

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H302-H315-H319-H335
防范說(shuō)明P261-P305+P351+P338
ADH-503;ADH503;ADH 503價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱(chēng)CAS號(hào)包裝價(jià)格
2024/11/08HY-15701BADH-503;ADH503;ADH 503
ADH-503
2055362-74-65mg550元
2024/11/08HY-15701BADH-503;ADH503;ADH 503
ADH-503
2055362-74-610mM * 1mLin DMSO630元
2024/11/08HY-15701BADH-503;ADH503;ADH 503
ADH-503
2055362-74-610mg900元

常見(jiàn)問(wèn)題列表

生物活性
ADH-503 ((Z)-Leukadherin-1 choline) 是一種具有口服活性的,變構(gòu)的 CD11b 激動(dòng)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(rùn)性免疫抑制骨髓細(xì)胞的數(shù)量,并增強(qiáng)樹(shù)突狀細(xì)胞的反應(yīng)。
靶點(diǎn)

CD11b

體外研究

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.

體內(nèi)研究

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.
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