232931-57-6
基本信息
(11A S,11A'S)-8,8'-(丙烷-1,3-二基雙(氧))雙(7-甲氧基-2-亞甲基-2,3-二氫-1H-苯并[E]吡咯[1,2-A][1,4]二氮雜卓-5(11AH)-酮)
SP-2001
BN-2629
CS-1384
UP 2001
SJG 136
NSC 694501
(11aS,11'aS)-8,8'-[1,3-Propanediylbis(oxy)]bis[1,2,3,11a-tetrahydro-7-methoxy-2-methylene-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-one
5H-Pyrrolo[2,1-c][1,4]benzodiazepin-5-one, 8,8'-[1,3-propanediylbis(oxy)]bis[1,2,3,11a-tetrahydro-7-methoxy-2-methylene-, (11aS,11'aS)-
物理化學(xué)性質(zhì)
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 |
2024/11/08 | HY-14573 | SJG 136 SJG-136 | 232931-57-6 | 1 mg | 2800元 |
2024/11/08 | HY-14573 | SJG 136 SJG-136 | 232931-57-6 | 5mg | 4900元 |
2024/11/08 | HY-14573 | SJG 136 SJG-136 | 232931-57-6 | 10mM * 1mLin DMSO | 6000元 |
常見(jiàn)問(wèn)題列表
XL50: 45 nM (pBR322 DNA)
SJG-136 (dimer 5) is a DNA cross-linking agent, with an XL 50 (concentration of agent required for 50% cross-linking of pBR322 DNA) of 45 nM for pBR322 DNA. SJG-136 is cytotoxic to ovarian cell lines, such as A2780 (IC 50 , 22.5 pM), A2780cisR (IC 50 , 24 pM), CH1 (IC 50 , 0.12 nM), CH1cisR (IC 50 , 0.6 nM), and SKOV-3 (IC 50 , 9.1 nM). SJG-136 (SG2000) also reduces the viability of a panel of canine cancer cells, with GI 50 values ranging from 0.33 - >100 nM after a 1 h exposure, and <0.03 - 17.33 nM following continuous exposure.
SJG-136 shows more potent antitumor effect against CMeC-1 tumour at 0.30 mg/kg than 0.15 mg/kg either as a single dose or administered once a week for three weeks via dosed intravenously in mice. SJG-136-induced H2AX phosphorylation shows good correspondence, but less sensitivity, than measurement of foci.