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Design, Synthesis, and Pharmacological Evaluation of R/S-3, 4-Dihydro-2, 2-dimethyl- 6-halo-4-(phenylaminocarbonylamino)-2H-1-benzopyrans: Toward Tissue-Selective Pancreatic Cell KATP Channel Openers Structurally Related to (()-Cromakalim

机译：r / s-3，4-二氢-2,2-二甲基-6-卤代-4-（苯氨基羰基氨基）-2h-1-苯并吡喃（苯并吡喃）的设计，合成和药理评价：朝向组织选择性胰腺Cell Katp通道开启器与（（）-cromakalim有关

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1. Design, synthesis, and pharmacological evaluation of R/S-3,4-dihydro-2,2-dimethyl-6-halo-4-(phenylaminocarbonylamino)-2H-1-benzopyrans: Toward tissue-selective pancreatic beta-cell K-ATP channel openers structurally related to (+/-)-cromakalim [J] . Sebille S, Gall D, de Tullio P, Journal of Medicinal Chemistry . 2006,第15期

机译：R / S-3,4-二氢-2,2-二甲基-6-卤代-4-（苯基氨基羰基氨基）-2H-1-苯并吡喃的设计，合成和药理学评估：向组织选择性胰腺β细胞K-与（+/-）-cromakalim结构相关的ATP通道开放剂
2. QSAR modelling of pancreatic beta-cell KATP channel openers R/S-3,4-dihydro-2,2-dimethyl-6-halo-4-(substituted phenylaminocarbonylamino)-2H-1-benzopyrans using MLR-FA techniques. [J] . Alam SM, Samanta S, Halder AK, European Journal of Medicinal Chemistry: Chimie Therapeutique . 2009,第1期

机译：使用MLR-FA技术对胰腺β细胞KATP通道开放剂R / S-3,4-二氢-2,2-二甲基-6-卤代4-（取代的苯基氨基羰基氨基）-2H-1-苯并吡喃进行QSAR建模。
3. Structural finding of R/S-3,4-dihydro-2,2-dimethyl-6-halo-4-(substituted phenylaminocarbonylamino)-2H-1-benzopyrans as selective pancreatic beta-cells K_(ATP-p beta)channel openers [J] . Sk.Mahasin Alam, Soma Samanta, Am it Kumar Haider Canadian Journal of Chemistry . 2007,第12期

机译：R / S-3,4-二氢-2,2-二甲基-6-卤代-4-（取代的苯基氨基羰基氨基）-2H-1-苯并吡喃作为选择性胰β-细胞K_（ATP-pβ）通道开放剂的结构发现
4. Design Synthesis and Pharmacological Evaluation of Haloperidol Derivatives as Novel Potent Calcium Channel Blockers with Vasodilator Activity [O] . Yicun Chen, Jinhong Zheng, Fuchun Zheng, 2011

机译：氟哌啶醇衍生物作为新型具有强效血管扩张活性的钙通道阻滞剂的设计合成及药理评价
5. Design, Synthesis, and Pharmacological Evaluation of R/S-3, 4-Dihydro-2, 2-dimethyl- 6-halo-4-(phenylaminocarbonylamino)-2H-1-benzopyrans: Toward Tissue-Selective Pancreatic Cell KATP Channel Openers Structurally Related to (()-Cromakalim [O] . -1

机译：r / s-3，4-二氢-2,2-二甲基-6-卤代-4-（苯氨基羰基氨基）-2h-1-苯并吡喃（苯并吡喃）的设计，合成和药理评价：朝向组织选择性胰腺Cell Katp通道开启器与（（）-cromakalim有关

Design, Synthesis, and Pharmacological Evaluation of R/S-3, 4-Dihydro-2, 2-dimethyl- 6-halo-4-(phenylaminocarbonylamino)-2H-1-benzopyrans: Toward Tissue-Selective Pancreatic Cell KATP Channel Openers Structurally Related to (()-Cromakalim

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