BCMCM-OH | 737830-16-9

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 香豆素及其衍生物
• 英文名称: BCMCM-OH
• CAS: 737830-16-9
• 化学式: C₂₃H₂₇ClO₁₀
• 分子量: 498.914
• InChiKey: LDXBKVNKIUBLIB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.11
• 重原子数：
  34.0
• 可旋转键数：
  8.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.48
• 拓扑面积：
  127.57
• 氢给体数：
  0.0
• 氢受体数：
  10.0

反应信息

• 作为反应物：
  描述：

  BCMCM-OH 在 N,N-二异丙基乙胺 、 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 反应 0.17h， 生成 (2S,3S)-3-benzyloxy-N-{[6,7-bis(carboxymethoxy)coumarin-4-yl-methoxy]carbonyl}aspartate
  参考文献：
  名称：

  Synthesis of carbamate-type caged derivatives of a novel glutamate transporter blocker

  摘要：

  L-threa-beta-Benzyloxyaspartate (L-TBOA) and (2S,3S)-3-{3-[4-(trifluoromethyl)benzoylamino]benzyloxy}aspartate (L-TFB-TBOA) are potent nontransportable blockers for glutamate transporters. We synthesized a carbamate-type coumarin derivative of L-TBOA 3a as a caged blocker and compared 3a with the corresponding ester-type analogs 1. The carbamate 3a was less sensitive to photolysis than the ester I but was more stable in the aqueous solution. The [6,7-bis(carboxymethoxy)-coumarin-4yl]methylcarbonyl (BCMCMC) group exhibited good results both in photoreactivity and stability. Therefore, we examined photolysis of N-BCMCMC-TBOA 3b and N-BCMCMC-TFB-TBOA 4, which immediately released blockers to show glutamate uptake inhibition. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2004.04.011
• 作为产物：
  描述：

  6,7-bis(tert-butoxycarbonylmethoxy)coumarin-4-carbaldehyde 在 sodium tetrahydroborate 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 5.0h， 生成 BCMCM-OH
  参考文献：
  名称：

  Synthesis of carbamate-type caged derivatives of a novel glutamate transporter blocker

  摘要：

  L-threa-beta-Benzyloxyaspartate (L-TBOA) and (2S,3S)-3-{3-[4-(trifluoromethyl)benzoylamino]benzyloxy}aspartate (L-TFB-TBOA) are potent nontransportable blockers for glutamate transporters. We synthesized a carbamate-type coumarin derivative of L-TBOA 3a as a caged blocker and compared 3a with the corresponding ester-type analogs 1. The carbamate 3a was less sensitive to photolysis than the ester I but was more stable in the aqueous solution. The [6,7-bis(carboxymethoxy)-coumarin-4yl]methylcarbonyl (BCMCMC) group exhibited good results both in photoreactivity and stability. Therefore, we examined photolysis of N-BCMCMC-TBOA 3b and N-BCMCMC-TFB-TBOA 4, which immediately released blockers to show glutamate uptake inhibition. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2004.04.011