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[(1R,2R,4S)-4-[(2R)-2-[(1R,9S,12SR,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32SR,35R)-1,18-dihydroxy-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-2,3,10,14,20-pentaoxo-11,36-dioxa-4-azatricyclo[30.3.1.0^4,9]hexatriaconta-16,24,26,28-tetraen-12-yl]propyl]-2-methoxycyclohexyl] N-(2-pyridylmethyl)carbamate | 156598-70-8

中文名称
——
中文别名
——
英文名称
[(1R,2R,4S)-4-[(2R)-2-[(1R,9S,12SR,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32SR,35R)-1,18-dihydroxy-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-2,3,10,14,20-pentaoxo-11,36-dioxa-4-azatricyclo[30.3.1.0^4,9]hexatriaconta-16,24,26,28-tetraen-12-yl]propyl]-2-methoxycyclohexyl] N-(2-pyridylmethyl)carbamate
英文别名
Rapamycin 42-ester with 2-pyridinylmethyl carbamic acid;[(1R,2R,4S)-4-[(2R)-2-[(1R,9S,12S,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32S,35R)-1,18-dihydroxy-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-2,3,10,14,20-pentaoxo-11,36-dioxa-4-azatricyclo[30.3.1.04,9]hexatriaconta-16,24,26,28-tetraen-12-yl]propyl]-2-methoxycyclohexyl] N-(pyridin-2-ylmethyl)carbamate
[(1R,2R,4S)-4-[(2R)-2-[(1R,9S,12SR,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32SR,35R)-1,18-dihydroxy-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-2,3,10,14,20-pentaoxo-11,36-dioxa-4-azatricyclo[30.3.1.0^4,9]hexatriaconta-16,24,26,28-tetraen-12-yl]propyl]-2-methoxycyclohexyl] N-(2-pyridylmethyl)carbamate化学式
CAS
156598-70-8
化学式
C58H85N3O14
mdl
——
分子量
1048.32
InChiKey
LSOCKOPBRQNFEN-BBSWHLIISA-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

计算性质

  • 辛醇/水分配系数(LogP):
    6.9
  • 重原子数:
    75
  • 可旋转键数:
    10
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    226
  • 氢给体数:
    3
  • 氢受体数:
    15

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • [EN] MTORC MODULATORS AND USES THEREOF<br/>[FR] MODULATEURS DE MTORC ET LEURS UTILISATIONS
    申请人:AEOVIAN PHARMACEUTICALS INC
    公开号:WO2020154447A1
    公开(公告)日:2020-07-30
    Novel rapamycin analogs and uses thereof are disclosed herein. The rapamycin analogs of the present disclosure show increased mTORC1 specificity and lowered mTORC2 specificity relative to rapamycin.
    本文披露了新型雷帕霉素类似物及其用途。本公开的雷帕霉素类似物相对于雷帕霉素表现出增加的mTORC1特异性和降低的mTORC2特异性。
  • Carbamates of rapamycin
    申请人:Wyeth
    公开号:EP1266900A1
    公开(公告)日:2002-12-18
    The invention concerns a compound of the structure wherein R1 and R2 are each, independently, hydrogen, -CONH-[(CR3R4)m(-A-(CR5R6)n)p]q-B; R3, R4, R5, R6, R9 and R10 are each defined substitutents, and R3-6 may each also represent hydrogen, B is alkenyl of 2-7 carbon atoms, alkynyl of 2-7 carbon atoms, hydroxyalkyl of 1-6 carbon atoms, alkylthioalkyl of 2-12 carbon atoms, alkylaminoalkyl of 2-12 carbon atoms, dialkylaminoalkyl of 3-12 carbon atoms, -OR7, -SR7, -CN, -COR7, -CONHR7, -OSO3R7, -NR7R8, -NHCOR7, -NHSO2R7, or Ar; A is -CH2-, -NR7-, -O-, -S-, -SO-, -PR7-, -NHCO-, -NHSO- or -P(O)(R7)-; Ar is naphthyl, pyridyl, quinolyl, isoquinolyl, quinoxalyl, thienyl, thionaphthyl, furyl, benzofuryl, benzodioxyl, benzoxazolyl, benzoisoxazolyl, indolyl, thiazolyl, isoxazolyl, pyrimidinyl, pyrazinyl, imidazolyl, benzopyranyl, benz[b]thiophenolyl, benzimidazolyl, benzthiazolyl, benzodioxolyl, piperidinyl, morpholinyl, piperazinyl, tetrahydrofuranyl, or pyrrolidinyl; wherein the Ar group may be optionally mono-, di-, or tri- substituted with a group selected from alkyl of 1-6 carbon atoms, arylalkyl of 7-10 carbon atoms, alkoxy of 1-6 carbon atoms, cyano, halo, hydroxy, nitro, carbalkoxy of 2-7 carbon atoms, trifluoromethyl, amino, dialkylamino of 1-6 carbon atoms per alkyl group, dialkylaminoalkyl of 3-12 carbon atoms, hydroxyalkyl of 1-6 carbon atoms, alkoxyalkyl of 2-12 carbon atoms, alkylthio of 1-6 carbon atoms, -SO3H -PO3H, and -CO2H; PO3H, and -CO2H; is a nitrogen containing heterocycle that may be saturated, unsaturated, or partially unsaturated, and may be optionally mono-, di-, or tri- substituted with a defined substituent, with the proviso that R1 and R2 are not both hydrogen; m=0-6; n=0-6; p=0-1; q=0-1; or a pharmaceutically acceptable salt thereof which is useful as an immunosuppressive, antiinflammatory, antifungal, antiproliferative, and antitumor agent.
    该发明涉及一种具有以下结构的化合物,其中R1和R2分别独立地为氢,-CONH-[(CR3R4)m(-A-(CR5R6)n)p]q-B;R3、R4、R5、R6、R9和R10均为定义的取代基,R3-6也可以分别表示氢,B为2-7个碳原子的烯基,2-7个碳原子的炔基,1-6个碳原子的羟基烷基,2-12个碳原子的烷硫基烷基,2-12个碳原子的烷基氨基烷基,3-12个碳原子的二烷基氨基烷基,-OR7,-SR7,-CN,-COR7,-CONHR7,-OSO3R7,-NR7R8,-NHCOR7,-NHSO2R7或Ar;A为-CH2-,-NR7-,-O-,-S-,-SO-,-PR7-,-NHCO-,-NHSO-或-P(O)(R7)-;Ar为萘基,吡啶基,喹啉基,异喹啉基,喹啉基,噻吩基,噻萘基,呋喃基,苯并呋喃基,苯二氧基基,苯氧唑基,苯并异唑基,吲哚基,噻唑基,异噁唑基,嘧啶基,吡啉基,咪唑基,苯并吡喃基,苯并噻吩基,苯并咪唑基,苯并噻唑基,苯二氧唑基,哌啶基,吗啉基,哌嗪基,四氢呋喃基或吡咯烷基;其中Ar基可以选择性地单取代、双取代或三取代,取代基可选自1-6个碳原子的烷基,7-10个碳原子的芳基烷基,1-6个碳原子的烷氧基,氰基,卤素,羟基,硝基,2-7个碳原子的羰基烷氧基,三氟甲基,氨基,1-6个碳原子的二烷基氨基,3-12个碳原子的二烷基氨基烷基,1-6个碳原子的羟基烷基,2-12个碳原子的烷氧基烷基,1-6个碳原子的烷硫基,-SO3H,-PO3H和-CO2H;PO3H和-CO2H;是一种含氮杂环,可以饱和、不饱和或部分不饱和,并且可以选择性地单取代、双取代或三取代具有定义的取代基,但R1和R2不能同时为氢;m=0-6;n=0-6;p=0-1;q=0-1;或其药学上可接受的盐,可用作免疫抑制剂、抗炎剂、抗真菌剂、抗增殖剂和抗肿瘤剂。
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同类化合物

马杜霉素II 雷帕霉素 长川霉素 达福普丁甲磺酸 西罗莫司脂化物 蛎灰菌素A 子囊霉素 威里霉素 唑他莫司 吡美莫司 双氢他克莫司 去甲氧基雷帕霉素 化合物 T32504 化合物 T25424 依维莫司 他克莫司杂质5 他克莫司31-DMT 他克莫司 乌米里莫斯 FK-506一水合物 8-表他克莫司 8,9,14,15,24,25,26,26alpha-八氢-14-羟基-4,12-二甲基-3-(1-甲基乙基)-(3R,4R,5E,10E,12E,14S,26alphaR)-3H-21,18-次氮基-1H,22H-吡咯并[2,1-c][1,8,4,19]二氧杂二氮杂二十四环-1,7,16,22(4H,17H)-四酮 42-O-[2-[[羟基[2-(三甲基铵)乙氧基]亚膦酰基]氧基]乙基]雷帕霉素内盐 42-(二甲基亚膦酰)雷帕霉素 42-(2-四唑基)雷帕霉素 40-O-[2-(叔丁基二甲硅基)氧代]乙基雷帕霉素 37-去亚甲基24,33-二-O-(叔-丁基二甲基硅烷基)-37-氧代-FK-506 31-O-去甲基-Fk506 28-O-甲基-雷帕霉素 24,33-二-O-(叔-丁基二甲基硅烷基)-37,38-去氢-37,38-二羟基-FK-506 24,32-双-O-(tert-butyldimethylsilyl)-他克莫司 22-羟基-33-叔-丁基二甲基硅烷基氧基-异-FK-506 2-甲氧基-5-硝基嘧啶-4-胺 19-表FK-506 15-O-去甲基长川霉素 13-O-去甲基子囊霉素 (E/Z)-FK-50626,28-烯丙酸酯 (2S,5S,6R,10R,11S)-10-庚基-6-羟基-4,11-二甲基-5-(苯基甲基)-2-丙-2-基-1,9-二氧杂-4-氮杂环十二烷-3,8,12-三酮 (1R,2R,4S)-4-{(2R)-2-[(1R,9S,12S,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32S,35R)-1,18-二羟基-19,30-二甲氧基-15,17,21,23,29,35-六甲基-2,3,10,14,20-五氧代-11,36-二氧杂-4-氮杂三环[30.3.1.04,9]三十六碳-16,24,26,28-四烯-12-基]丙基}-2-甲氧基环己基2,2,5-三甲基-1,3-二恶烷-5-羧酸酯 (21S)-1-aza-4,4-dimethyl-6,19-dioxa-2,3,7,20-tetraoxobicyclo<19.4.0>pentacosane CCI-779 boronate rapamycin (-)-spongedepsin (1R,9S,12SR,15R,16E,18R,19R,21R,23S,24E,26E,28E,32SR,35R)-1,18-dihydroxy-30-(3-hydroxypropoxy)-19-methoxy-12-[(1R)-2-[(1S,3R,4R)-3-methoxy-4-(3-phenylpropoxy)cyclohexyl]-1-methylethyl]-15,17,21,23,29,35-hexamethyl-11,36-dioxa-4-azatricyclo[30.3.1.0^4,9]hexatriaconta-16,24,26,28-tetraene-2,3,10,14,20-pentone rapamycin 42-hemiadipate Rapamycin 42-ester with 4-methylpiperazine-1-carboxylic acid rapamycin O-[(S)-2,3-dihydroxypropyloxycarbonyl]rapamycin 29-epirapamycin 40-O-tert-butyldimethylsilyl rapamycin