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2361659-61-0

中文名稱(chēng) AES-135
英文名稱(chēng) Benzamide, 4-[[[4-(1,1-dimethylethyl)phenyl]methyl][2-[[(4-fluorophenyl)sulfonyl][(2,3,4,5,6-pentafluorophenyl)methyl]amino]acetyl]amino]-N-hydroxy-
CAS 2361659-61-0
分子式 C33H29F6N3O5S
分子量 693.66
MOL 文件 2361659-61-0.mol
2361659-61-0 結(jié)構(gòu)式 2361659-61-0 結(jié)構(gòu)式

基本信息

中文別名
化合物AES-135
英文別名
Benzamide, 4-[[[4-(1,1-dimethylethyl)phenyl]methyl][2-[[(4-fluorophenyl)sulfonyl][(2,3,4,5,6-pentafluorophenyl)methyl]amino]acetyl]amino]-N-hydroxy-

物理化學(xué)性質(zhì)

儲(chǔ)存條件-20°C儲(chǔ)存
溶解度DMSO : 100 mg/mL (144.16 mM; Need ultrasonic)
形態(tài)Solid
顏色White to off-white
AES-135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
2026/06/05HY-114483AES-135
AES-135
2361659-61-01 mg745元
2026/06/05HY-114483AES-135
AES-135
2361659-61-05 mg1938元
2026/06/05HY-114483AES-135
AES-135
2361659-61-010 mg2838元

常見(jiàn)問(wèn)題列表

生物活性
AES-135 是一種基于羥肟酸的 HDAC 抑制劑,可延長(zhǎng)胰腺癌原位小鼠模型的存活時(shí)間。AES-135 抑制 HDAC3、HDAC6、HDAC8 和 HDAC11,IC50 范圍為190-1100 nM。
靶點(diǎn)

HDAC6

190 nM (IC 50 )

HDAC11

636 nM (IC 50 )

HDAC3

654 nM (IC 50 )

HDAC8

1100 nM (IC 50 )

體外研究

AES-135 inhibits cancer cells growth with IC 50 values of 2.3 μM, 1.4 μM, 0.27 μM, 0.94 μM, 1.9 μM, 2.72 μM, 2.1 μM, 15.0 μM, 1.6 μM and 19.2 μM for BT143, BT189, D425, D458, MV4-11, MOLM-13, MDA-MB-231, K562, PC-3 and MRC-9 cells, respectively.

體內(nèi)研究

AES-135 (50 mg/kg; intraperitoneal injection; 5 days a week; for 1 month) treatment significantly increases survival of C57Bl/6 mice implanted with KPC2 cells.
NSG mice are dosed with a single 20 mg/kg intraperitoneal (IP) injection, and blood is taken at 0.5 h, 1 h, 2 h, 4 h, 8 h, and 24 h. AES-135 achieved μM concentrations in the blood, reaching C max 7452 ng/mL (10.74 μM) within 30 min, which is sustained for 8 h. The blood concentration of AES-135 is dose dependent, achieving an average of 323 ng/mL (0.47 μM) with 10 mg/kg dosing and 1829 ng/mL (2.64 μM) with 40 mg/kg. AES-135 shows an impressive pharmacokinetic profile in mice with an in vivo half-life of 5.0 h.

Animal Model: C57Bl/6 mice injected with KPC2 cells
Dosage: 50 mg/kg
Administration: Intraperitoneal injection; 5 days a week; for 1 month
Result: Significantly increased survival of mice.
"2361659-61-0" 相關(guān)產(chǎn)品信息
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