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232931-57-6

中文名稱(chēng) SJG 136
英文名稱(chēng) BN-2629
CAS 232931-57-6
分子式 C31H32N4O6
分子量 556.61
MOL 文件 232931-57-6.mol
更新日期 2024/12/17 16:14:28
232931-57-6 結(jié)構(gòu)式 232931-57-6 結(jié)構(gòu)式

基本信息

中文別名
(11AS,11'AS)-8,8'-[1,3-丙二基雙(氧基)]雙[1,2,3,11A-四氫-7-甲氧基-2-亞甲基-5H-吡咯并[2,1-C] [1,4]苯并二氮雜-5-酮]
(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)
英文別名
SG2000
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)-
所屬類(lèi)別
生物化工:激動(dòng)劑抑制劑

物理化學(xué)性質(zhì)

沸點(diǎn)805.5±65.0 °C(Predicted)
密度1.36±0.1 g/cm3(Predicted)
儲(chǔ)存條件Sealed in dry,Room Temperature
溶解度DMSO: ≥ 100 mg/mL (179.66 mM)
酸度系數(shù)(pKa)3.88±0.20(Predicted)
形態(tài)Solid
顏色Off-white to yellow

安全數(shù)據(jù)

SJG 136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-14573SJG 136
SJG-136
232931-57-61 mg2800元
2024/11/08HY-14573SJG 136
SJG-136
232931-57-65mg4900元
2024/11/08HY-14573SJG 136
SJG-136
232931-57-610mM * 1mLin DMSO6000元

常見(jiàn)問(wèn)題列表

生物活性
SJG-136 是一種有效的 DNA 交聯(lián)劑 (DNA crosslinker),與 pBR322 DNA 交聯(lián)的 XL50 值為 45 nM。SJG-136 具有抗腫瘤作用。
靶點(diǎn)

XL50: 45 nM (pBR322 DNA)

體外研究

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.

體內(nèi)研究

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.

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