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2,3-dimethyl-5-benzylfuran | 250609-52-0

中文名称
——
中文别名
——
英文名称
2,3-dimethyl-5-benzylfuran
英文别名
5-benzyl-2,3-dimethylfuran;2-benzyl-4,5-dimethylfuran;2-Benzyl4,5-dimethylfuran
2,3-dimethyl-5-benzylfuran化学式
CAS
250609-52-0
化学式
C13H14O
mdl
——
分子量
186.254
InChiKey
FRLNGHBISDFXOX-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    266.3±9.0 °C(Predicted)
  • 密度:
    1.011±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    13.1
  • 氢给体数:
    0
  • 氢受体数:
    1

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2,3-dimethyl-5-benzylfuran二甲基硫氧气rose bengal 作用下, 反应 2.5h, 生成 4-hydroxy-3,4-dimethyl-5-phenylcyclopent-2-enone
    参考文献:
    名称:
    简单呋喃从一锅到水中的4-羟基-2-环戊烯酮的转化
    摘要:
    使用单线态氧作为氧化剂,已开发出一种高效易用的一锅易得的呋喃在H 2 O中转化为4-羟基-2-环戊烯酮的方法。
    DOI:
    10.1002/anie.201407477
  • 作为产物:
    描述:
    2,3-dimethylfuran溴甲苯正丁基锂 作用下, 以 四氢呋喃正己烷 为溶剂, 反应 13.0h, 以68%的产率得到2,3-dimethyl-5-benzylfuran
    参考文献:
    名称:
    简单呋喃从一锅到水中的4-羟基-2-环戊烯酮的转化
    摘要:
    使用单线态氧作为氧化剂,已开发出一种高效易用的一锅易得的呋喃在H 2 O中转化为4-羟基-2-环戊烯酮的方法。
    DOI:
    10.1002/anie.201407477
点击查看最新优质反应信息

文献信息

  • Naphtho[2,3-B]heteroar-4-yl derivatives
    申请人:American Home Products Corporation
    公开号:US06121271A1
    公开(公告)日:2000-09-19
    This invention provides compounds of Formula I having the structure wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, W, R.sup.9, X, R.sup.6, p, Y, Z, R.sup.7, and R.sub.8 are as defined in the specification, or a pharmaceutically acceptable salt thereof, which are useful in treating metabolic disorders related to insulin resistance or hyperglycemia.
    这项发明提供了具有结构的化合物,其中R.sup.1、R.sup.2、R.sup.3、R.sup.4、R.sup.5、W、R.sup.9、X、R.sup.6、p、Y、Z、R.sup.7和R.sub.8如规范中定义,或其药用盐,可用于治疗与胰岛素抵抗或高血糖相关的代谢紊乱。
  • Furans, benzofurans, and thiophenes useful in the treatment of insulin
    申请人:American Home Products Corporation
    公开号:US06103708A1
    公开(公告)日:2000-08-15
    This invention provides compounds of Formula I having the structure: ##STR1## wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, R.sup.8, W, X, Y, and Z are as defined in the specification, or a pharmaceutically acceptable salt thereof, which are useful in treating metabolic disorders related to insulin resistance or hyperglycemia.
    这项发明提供了具有结构的Formula I的化合物:##STR1##其中R.sup.1、R.sup.2、R.sup.3、R.sup.4、R.sup.5、R.sup.6、R.sup.7、R.sup.8、W、X、Y和Z如规范中所定义,或其药学上可接受的盐,这些化合物在治疗与胰岛素抵抗或高血糖相关的代谢紊乱方面是有用的。
  • Benzothiophenes, benzofurans, and indoles useful in the treatment of insulin resistance and hyperglycemia
    申请人:American Home Products Corporation
    公开号:US06251936B1
    公开(公告)日:2001-06-26
    This invention provides compounds of Formula I having the structure E is S, SO, SO2, O, or NR1c; X is hydrogen, halogen, alkyl of 1-6 carbon atoms, alkenyl of 2-7 carbon atoms, CN, aryl, aralkyl of 6-12 carbon atoms, hydroxyalkyl of 1-6 carbon atoms, hydroxyaralkyl of 6-12 carbon atoms, perfluoroalkyl of 1-6 carbon atoms, alkoxy of 1-6 carbon atoms, aryloxy; arylalkoxy, nitro, amino, NR2R2a, NR2COR2a, cycloalkylamino of 3-8 carbon atoms, morpholino, alkylsulfanyl of 1-6 carbon atoms, arylsulfanyl, pyridylsulfanyl, 2-N,N-dimethylaminoethylsulfanyl, —OCH2CO2R2b or —COR2c; Z1 and Z2 are each, independently, hydrogen, halogen, CN, alkyl of 1-6 carbon atoms, aryl, aralkyl of 6-12 carbon atoms, cycloalkyl of 3-8 carbon atoms, nitro, amino, —NR1R1a, —NR1COR1a, cycloalkylamino of 3-8 carbon atoms, morpholino, or OR8, or Z1 and Z2 may be taken together as a diene unit having the formula —CH═CR9—CR10═CR11—; or a pharmaceutically acceptable salt thereof, which are useful in treating metabolic disorders related to insulin resistance or hyperglycemia.
    这项发明提供了具有结构的I型化合物,其中E为S、SO、SO2、O或NR1c;X为氢、卤素、1-6碳原子的烷基、2-7碳原子的烯基、CN、芳基、6-12碳原子的芳基烷基、1-6碳原子的羟基烷基、6-12碳原子的羟基芳基烷基、1-6碳原子的全氟烷基、1-6碳原子的烷氧基、芳氧基、芳基烷氧基、硝基、基、NR2R2a、NR2COR2a、3-8碳原子的环烷基基、吗啡啉、1-6碳原子的烷基基、芳基基、吡啶基、2-N,N-二甲基基乙基、—OCH2CO2R2b或—COR2c;Z1和Z2分别独立地为氢、卤素、CN、1-6碳原子的烷基、芳基、6-12碳原子的芳基烷基、3-8碳原子的环烷基、硝基、基、—NR1R1a、—NR1COR1a、3-8碳原子的环烷基基、吗啡啉或OR8,或Z1和Z2可以作为具有式—CH═CR9—CR10═CR11—的二烯单位一起取;或其药学上可接受的盐,用于治疗与胰岛素抵抗或高血糖相关的代谢紊乱。
  • Benzothiophenes, benzofurans, and indoles useful in the treatment of insulin-resistance and hyperglycemia
    申请人:——
    公开号:US20020002187A1
    公开(公告)日:2002-01-03
    This invention provides compounds of Formula I having the structure 1 A is hydrogen, halogen, or OH; B and D are each, independently, hydrogen, halogen, CN, alkyl of 1-6 carbon atoms, aryl, aralkyl of 6-12 carbon atoms, hydroxyalkyl of 1-6 carbon atoms, hydroxyaralkyl of 6-12 carbon atoms, cycloalkyl of 3-8 carbon atoms, nitro, amino, —NR 1 R 1a , —NR 1 COR 1a , —NR 1 CO 2 R 1a , cycloalkylamino of 3-8 carbon atoms, morpholino, furan-2-yl, furan-3-yl, thiophen-2-yl, thiophen-3-yl, —COR 1b or OR; R is hydrogen, alkyl of 1-6 carbon atoms, —COR 1 , —(CH 2 ) n CO 2 R 1 , —CH(R 1a )CO 2 R 1 , —SO 2 R 1 , —(CH 2 ) m CH(OH)CO 2 R 1 , —(CH 2 ) m COCO 2 R 1 , —(CH 2 ) m CH═CHCO 2 R 1 , or —(CH 2 ) m O(CH 2 )CO 2 R 1 ; R 1 is hydrogen, alkyl of 1-6 carbon atoms, aralkyl of 6-12 carbon atoms, aryl, or CH 2 CO 2 R 1 ; R 1′ is hydrogen or alkyl of 1-6 carbon atoms E is S, SO, SO 2 , O, or NR 1c ; X is hydrogen, halogen, alkyl of 1-6 carbon atoms, alkenyl of 2-7 carbon atoms, CN, aryl, aralkyl of 6-12 carbon atoms, hydroxyalkyl of 1-6 carbon atoms, hydroxyaralkyl of 6-12 carbon atoms, perfluoroalkyl of 1-6 carbon atoms, alkoxy of 1-6 carbon atoms, aryloxy; arylalkoxy, nitro, amino, NR 2 R 2a , NR 2 COR 2a , cycloalkylamino of 3-8 carbon atoms, morpholino, alkylsulfanyl of 1-6 carbon atoms, arylsulfanyl, pyridylsulfanyl, 2-N,N-dimethylaminoethylsulfanyl, —OCH 2 CO 2 R 2b or —COR 2c ; Y is hydrogen, halogen, alkyl of 1-6 carbon atoms, aryl, aralkyl of 6-12 carbon atoms, hydroxyalkyl of 1-6 carbon atoms, hydroxyaralkyl of 6-12 carbon atoms, —OR 3 , SR 3 , NR 3 R 3a , —COR 3b , morpholine or piperidine; R 1a , R 1c , R 2 , R 2a R 3 , R 3a are each, independently, hydrogen, alkyl of 1-6 carbon atoms, aralkyl of 6-12 carbon atoms, or aryl; R 1b is alkyl of 1-6 carbon atoms or aryl; R 2b is hydrogen, alkyl of 1-6 carbon atoms; R 2c and R 3b are each, independently, alkyl of 1-6 carbon atoms, aryl, or aralkyl of 6-12 carbon atoms; C is hydrogen, halogen or OR 4 ; R 4 is hydrogen, alkyl of 1-6 carbon atoms, —CH(R 5 )W, —C(CH 3 ) 2 CO 2 R 6 , 5-thiazolidine-2,4-dione, —CH(R 7 )(CH 2 ) m CO 2 R 6 , —COR 6 , —PO 3 (R 6 ) 2 , —SO 2 R 6 , —(CH 2 ) p CH(OH)CO 2 R 6 , —(CH 2 ) p COCO 2 R 6 , —(CH 2 ) p CH═CHCO 2 R 6 , or —(CH2) p O(CH 2 ) q CO 2 R 6 ; R 5 is hydrogen, alkyl of 1-6 carbon atoms, aralkyl of 6-12 carbon atoms, aryl, —CH 2 (1H-imidazol-4-yl), —CH 2 (3-1H-indolyl), —CH 2 CH 2 (1,3-dioxo-1,3-dihydro-isoindol-2-yl), —CH 2 CH 2 (1-oxo-1,3-dihydro-isoindol-2-yl), —CH 2 (3-pyridyl), —CH 2 CO 2 H, or —(CH 2 ) n G; G is NR 6a R 7a , NR 6a COR 7a , 2 W is CO 2 R 6 , CONH 2 , CONHOH, CN, CONH(CH 2 ) 2 CN, 5-tetrazole, —PO 3 (R 6 ) 2 , —CH 2 OH, —CONR 6b CHR 7b , —CH 2 NR 6b CHR 7b CO 2 R 6 , —CH 2 OCHR 7b CO 2 R 6 —CH 2 Br, or —CONR 6b CHR 7b CO 2 R 6 ; R 6 , R 6a , R 7 , R 7a are each, independently, is hydrogen, alkyl of 1-6 carbon atoms, or aryl; R 6b is hydrogen or —COR 6c ; R 6c is alkyl of 1-6 carbon atoms or aryl; R 7b is hydrogen, alkyl of 1-6 carbon atoms, or hydroxyalkyl of 1-6 carbon atoms; Z 1 and Z 2 are each, independently, hydrogen, halogen, CN, alkyl of 1-6 carbon atoms, aryl, aralkyl of 6-12 carbon atoms, cycloalkyl of 3-8 carbon atoms, nitro, amino, —NR 1 R 1a , —NR 1 COR 1a , cycloalkylamino of 3-8 carbon atoms, morpholino, or OR 8 , or Z 1 and Z 2 may be taken together as a diene unit having the formula —CH═CR 9 —CR 10 ═CR 11 —; R 8 is hydrogen, alkyl of 1-6 carbon atoms, or aryl; R 9 , R 10 , and R 11 are each, independently, hydrogen, alkyl of 1-6 carbon atoms, aryl, halogen, hydroxy, or alkoxy of 1-6 carbon atoms m is 1 to 4 n is 1 or 2; p is 1 to 4; q is 1 to 4; or a pharmaceutically acceptable salt thereof, which are useful in treating metabolic disorders related to insulin resistance or hyperglycemia.
    本发明提供了具有结构式I的化合物: 其中1A是氢、卤素或OH; B和D分别是氢、卤素、CN、1-6个碳原子的烷基、6-12个碳原子的芳基、6-12个碳原子的芳基烷基、1-6个碳原子的羟基烷基、6-12个碳原子的羟基芳基烷基、3-8个碳原子的环烷基、硝基、基、—NR1R1a、—NR1COR1a、—NR1CO2R1a、3-8个碳原子的环烷基基、吗啉基、呋喃-2-基、呋喃-3-基、噻吩-2-基、噻吩-3-基、—COR1bor OR; R是氢、1-6个碳原子的烷基、—COR1、—(CH2)nCO2R1、—CH(R1a)CO2R1、—SO2R1、—( )mCH(OH)CO2R1、—( )mCOCO2R1、—( )mCH═CHCO2R1或—( )mO( )CO2R1; R1是氢、1-6个碳原子的烷基、6-12个碳原子的芳基烷基、芳基或 CO2R1; R1'是氢或1-6个碳原子的烷基; E是S、SO、SO2、O或NR1c; X是氢、卤素、1-6个碳原子的烷基、2-7个碳原子的烯基、CN、6-12个碳原子的芳基烷基、1-6个碳原子的羟基烷基、6-12个碳原子的羟基芳基烷基、1-6个碳原子的全氟烷基、1-6个碳原子的烷氧基、芳氧基、芳基烷氧基、硝基、基、NR2R2a、NR2COR2a、3-8个碳原子的环烷基基、吗啉基、1-6个碳原子的烷基醇、芳基醇、吡啶醇、2-N,N-二甲基基乙基醇、—O CO2R2bor—COR2c; Y是氢、卤素、1-6个碳原子的烷基、芳基、6-12个碳原子的芳基烷基、1-6个碳原子的羟基烷基、6-12个碳原子的羟基芳基烷基、—OR3、SR3、NR3R3a、—COR3b、吗啉或哌啶; R1a、R1c、R2、R2a、R3、R3a各自独立地是氢、1-6个碳原子的烷基、6-12个碳原子的芳基烷基或芳基; R1b是1-6个碳原子的烷基或芳基; R2b是氢或1-6个碳原子的烷基; R2c和R3b各自独立地是1-6个碳原子的烷基、芳基或6-12个碳原子的芳基烷基; C是氢、卤素或OR4; R4是氢、1-6个碳原子的烷基、—CH(R5)W、—C(CH3)2CO2R6、5-噻唑烷-2,4-二酮、—CH(R7)( )mCO2R6、—COR6、—PO3(R6)2、—SO2R6、—( )pCH(OH)CO2R6、—( )pCOCO2R6、—( )pCH═CHCO2R6或—( )pO( )qCO2R6; R5是氢、1-6个碳原子的烷基、6-12个碳原子的芳基烷基、芳基、— (1H-咪唑-4-基)、— (3-1H-吲哚基)、— (1,3-二氢-2-氮杂-2-基)、— (1-氧代-1,3-二氢-2-氮杂-2-基)、— (3-吡啶基)、— CO2H或—( )nG; G是NR6aR7a、NR6aCOR7a、2W是CO2R6、CONH2、CONHOH、CN、CONH( )2CN、5-四唑、—PO3(R6)2、— OH、—CONR6bCHR7b、— NR6bCHR7bCO2R6、— OCHR7bCO2R6— Br或—CONR6bCHR7bCO2R6; R6、R6a、R7、R7a各自独立地是氢、1-6个碳原子的烷基或芳基; R6b是氢或—COR6c; R6c是1-6个碳原子的烷基或芳基; R7b是氢、1-6个碳原子的烷基或1-6个碳原子的羟基烷基; Z1和Z2各自独立地是氢、卤素、CN、1-6个碳原子的烷基、芳基、6-12个碳原子的芳基烷基、3-8个碳原子的环烷基、硝基、基、—NR1R1a、—NR1COR1a、3-8个碳原子的环烷基基、吗啉基或OR8,或Z1和Z2可以作为具有式—CH═CR9—CR10═CR11—的二烯单元一起取代; R8是氢、1-6个碳原子的烷基或芳基; R9、R10和R11各自独立地是氢、1-6个碳原子的烷基、芳基、卤素、羟基或1-6个碳原子的烷氧基; m为1至4; n为1或2; p为1至4; q为1至4; 或其药学上可接受的盐,其用于治疗与胰岛素抵抗或高血糖相关的代谢紊乱。
  • Furans, benzofurans, and thiophenes useful in the treatment of insulin resistance and hyperglycemia
    申请人:American Home Products Corporation
    公开号:US20020035272A1
    公开(公告)日:2002-03-21
    This invention provides compounds of Formula I having the structure 1 wherein R 1 and R 2 are each, independently, hydrogen, alkyl of 1-6 carbon atoms, halogen, perfluoroalkyl of 1-6 carbon atoms, cycloalkyl of 3-8 carbon atoms, thienyl, furyl, phenyl or phenyl substituted with trifluoromethyl, chloro, methoxy, or trifluoromethoxy; R 3 and R 4 are each, independently, hydrogen, carboxyl, hydroxyl, hydoxyalkyl of 1-6 carbon atoms, alkoxy of 1-6 carbon atoms, perfluoroalkoxy of 1-6 carbon atoms, alkanoyloxy of 2-7 carbon atoms, perfluoroalkanoyloxy of 2-7 carbon atoms, arylalkoxy of 7-15 carbon atoms, aryloxy of 6-12 carbon atoms, aroyloxy of 6-12 carbon atoms, aryloxycarbonyl of 7-13 carbon atoms, alkoxycarbonyl of 2-7 carbon atoms, perfluoroalkoxycarbonyl of 2-7 carbon atoms, alkyl of 1-6 carbon atoms, perfluoroalkyl of 1-6 carbon atoms, alkylamino of 1-6 carbon atoms, dialkylamino of 1-6 carbon atoms per alkyl group, tetrazolyl, mercapto, nitrile, nitro, amino, —NHSO 2 CF 3 , carbamoyl, carboxyaldehyde, halogen, acylamino, 3-hydroxy-cyclobut-3-ene-4-yl-1,2-dione, pyridyl, isoxazolyl, pyrimidyl or pyrimidyl substituted with mercapto, or tetronic acid; R 5 is hydrogen, alkyl of 1-6 carbon atoms, perfluoroalkyl of 1-6 carbon atoms, naphthalenylmethyl, benzyl or benzyl substituted with halogen, R 6 and R 7 are each, independently, hydrogen, alkyl of 1-6 carbon atoms, or perfluoroalkyl of 1-6 carbon atoms, or R 6 and R 7 may be taken together as a diene unit having the structure —CH═CH—CH═CH—; W is S or O, X is —NR 8 CH 2 —, —NR 8 —, or O; R 8 is hydrogen or alkyl; Y is carbonyl, methylene, ethyl, or —NHCH 2 —; Z is phenyl, pyridyl, naphthyl, thienyl, furyl, pyrrolyl, pyrazolyl, isoxazolyl, or isothiazolyl; or a pharmaceutically acceptable salt thereof, which are useful in treating metabolic disorders related to insulin resistance or hyperglycemia.
    本发明提供了具有结构1的化合物,其中R1和R2分别独立地为氢、1-6碳原子的烷基、卤素、1-6碳原子的全氟烷基、3-8碳原子的环烷基、噻吩基、呋喃基、苯基或经三甲基、、甲氧基或三甲氧基取代的苯基;R3和R4分别独立地为氢、羧基、羟基、1-6碳原子的羟基烷基、1-6碳原子的烷氧基、1-6碳原子的全氟烷氧基、2-7碳原子的烷酰氧基、2-7碳原子的全氟烷酰氧基、7-15碳原子的芳基烷氧基、6-12碳原子的芳基氧基、6-12碳原子的芳酰氧基、7-13碳原子的芳基氧羰基、2-7碳原子的烷氧羰基、2-7碳原子的全氟烷氧羰基、1-6碳原子的烷基、1-6碳原子的全氟烷基、1-6碳原子的烷基基、每个烷基基团为1-6碳原子的双烷基基、四唑基、巯基、腈基、硝基、基、—NHSO2CF3、基甲酰基、羧醛基、卤素、酰胺基、3-羟基环丁-3-烯-4-基-1,2-二酮、吡啶基、异噁唑基、嘧啶基或经巯基取代的嘧啶基或四酮酸;R5为氢、1-6碳原子的烷基、1-6碳原子的全氟烷基、基甲基、苄基或经卤素取代的苄基;R6和R7分别独立地为氢、1-6碳原子的烷基或1-6碳原子的全氟烷基,或R6和R7可以一起作为具有结构—CH═CH—CH═CH—的二烯基单元;W为S或O,X为—NR8CH2—、—NR8—或O;R8为氢或烷基;Y为羰基、亚甲基、乙基或—NHCH2—;Z为苯基、吡啶基、基、噻吩基、呋喃基、吡咯基、吡唑基、异噁唑基或异硫氰酸基;或其药学上可接受的盐,可用于治疗与胰岛素抵抗或高血糖相关的代谢紊乱。
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同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫