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S27096

JNJ-7777120

源葉(MedMol) 98%
  • 英文名:
  • 1-[(5-Chloro-1H-indol-2-yl)carbonyl]-4-methylpiperazine
  • 別名:
  • (5-氯-1H-吲哚-2-基)(4-甲基哌嗪-1-基)甲酮;JNJ7777120
  • CAS號:
  • 459168-41-3
  • 分子式:
  • C14H16ClN3O
  • 分子量:
  • 277.75
  • 核磁/質(zhì)譜:
品牌貨號產(chǎn)品規(guī)格價(jià)格(RMB) 庫存(上海) 北京 武漢 南京 數(shù)量計(jì)量單位 加入購物車...
源葉(MedMol) S27096-5mg 98% ¥400.00元 6 - - - EA 加入購物車
源葉(MedMol) S27096-10mg 98% ¥600.00元 5 - - - EA 加入購物車
源葉(MedMol) S27096-25mg 98% ¥1120.00元 6 - - - EA 加入購物車
源葉(MedMol) S27096-100mg 98% ¥3040.00元 預(yù)計(jì)交期:2-3天 - - - EA 加入購物車
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產(chǎn)品介紹

參考文獻(xiàn)

質(zhì)檢證書(COA)

摩爾濃度計(jì)算器

相關(guān)產(chǎn)品

  • 產(chǎn)品描述: JNJ-7777120 is a potent and selective histamine H4 receptor antagonist (Ki=4.5 nM). JNJ-7777120 effectively blocks histamine-induced migration of mouse tracheal mast cells from connective tissue to epithelial cells. JNJ-7777120 also significantly blocks neutrophil infiltration in a mouse Zymosan-induced peritonitis model. JNJ-7777120 has a good potential to study antipruritic and anti-inflammatory
  • 靶點(diǎn): H4 receptor;HistamineReceptor
  • 體內(nèi)研究:
    JNJ-7777120 shows equipotent against the human, mouse, and rat receptors and exhibits at least 1000-fold selectivity over H1, H2, or H3 receptors. JNJ-7777120 has an oral bioavailability of ~30% in rats and 100% in dogs, with a half-life of ~3 h in both species. JNJ-7777120 (20 mg/kg; s.c.; single daily for 2 days) blocks the histamine-induced migration of tracheal mast cells from the connective tissue toward the epithelium in mice. JNJ-7777120 (10 mg/kg; s.c.; single) significantly blocks neutrophil infiltration in a mouse zymosan-induced peritonitis model. Animal Model: BALB/c mice. Dosage: 20 mg/kg Administration: Subcutaneous injection; single daily for 2 days Result: Blocked histamine induced an increase in the number of mast cells per tracheal section and a significant migration of mast cells towards the tracheal epithelium. Animal Model: Male outbred Swiss albino mice (zymosan-induced peritonitis model). Dosage: 10 mg/kg Administration: Subcutaneous injection; single Result: Led to a statistically significant reduction of neutrophil infiltration.
  • 參考文獻(xiàn):
    1. Thurmond RL, et al. A potent and selective histamine H4 receptor antagonist with anti-inflammatory properties. J Pharmacol Exp Ther. 2004 Apr;309(1):404-13. 2. Ohsawa Y, et al. The antagonism of histamine H1 and H4 receptors ameliorates chronic allergic dermatitis via anti-pruritic and anti-inflammatory effects in NC/Nga mice. Allergy. 2012 Aug;67(8):1014-22.
  • 溶解性: Soluble  in  DMSO
  • 保存條件: 2-8℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 3.6 ml 18.002 ml 36.004 ml
    5 mM 0.72 ml 3.6 ml 7.201 ml
    10 mM 0.36 ml 1.8 ml 3.6 ml
    50 mM 0.072 ml 0.36 ml 0.72 ml
  • 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。
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