92950-42-0 (焦谷氨酰丙氨酸,13-Oxo-10-deacetyl Baccatin III)

CAS号:
92950-42-0
中文名称:
焦谷氨酰丙氨酸
英文名称:
13-Oxo-10-deacetyl Baccatin III
分子式:
C29H34O10
分子量:
542.574269771576

焦谷氨酰丙氨酸(92950-42-0)名称与标识符

名称

中文别名:
10-脱乙酰基13-氧代浆果赤霉素Ⅲ;焦谷氨酰丙氨酸;
英文别名:
13-Oxo-10-deacetyl Baccatin III;10-Deacetyl-13-oxobaccatin III;13-Oxo-10-deacetyl B;(2aR,4S,4aS,6R,11S,12S,12aR,12bS)-12b-(Acetyloxy)-12-(benzoyloxy)-2a,4,4a,10,11,12,12a,12b-octahydro-4,6,11-trihydroxy-4a,8,13,13-tetramethyl-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxete-5,9(3H,6H)-dione (ACI);7,11-Methano-1H-cyclodeca[3,4]benz[1,2-b]oxete-5,9(3H,6H)-dione, 12b-(acetyloxy)-12-(benzoyloxy)-2a,4,4a,10,11,12,12a,12b-octahydro-4,6,11-trihydroxy-4a,8,13,13-tetramethyl-, [2aR-(2aα,4β,4aβ,6β,11α,12α,12aα,12bα)]- (ZCI);

标识符

InChIKey:
WMZBAMYUOYXRSF-RIFKXWPOSA-N
Inchi:
1S/C29H34O10/c1-14-17(31)12-29(36)24(38-25(35)16-9-7-6-8-10-16)22-27(5,23(34)21(33)20(14)26(29,3)4)18(32)11-19-28(22,13-37-19)39-15(2)30/h6-10,18-19,21-22,24,32-33,36H,11-13H2,1-5H3/t18-,19+,21+,22-,24-,27+,28-,29+/m0/s1
SMILES:
O([C@@]12CO[C@@H]1C[C@H](O)[C@@]1([C@@H]2[C@@H]([C@@]2(CC(=O)C(C)=C([C@H](C1=O)O)C2(C)C)O)OC(C1C=CC=CC=1)=O)C)C(=O)C

焦谷氨酰丙氨酸(92950-42-0)物化性质

实验特性

  • LogP : 1.29000
  • PSA : 156.66000

计算特性

  • 精确分子量 : 542.21500

焦谷氨酰丙氨酸(92950-42-0)推荐厂家 更多厂家(31)

焦谷氨酰丙氨酸(92950-42-0)合成路线

合成路线:1 步
反应条件:
参考文献:
Diastereoselective 14β-Hydroxylation of Baccatin III Derivatives
Baldelli, Eleonora; Battaglia, Arturo; Bombardelli, Ezio; Carenzi, Giacomo; Fontana, Gabriele; et al, Journal of Organic Chemistry, 2003, 68(25), 9773-9779
合成路线:1 步
反应条件:
参考文献:
A process for the preparation of 14--hydroxybaccatin III 1,14-carbonate
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Baccatin III derivatives: reduction of the C-11, C-12 double bond
Marder, Raphaele; Dubois, Joelle; Guenard, Daniel; Gueritte-Voegelein, Francoise; Potier, Pierre, Tetrahedron, 1995, 51(7), 1985-94
合成路线:1 步
反应条件:
参考文献:
The chemistry of occurrence of taxane derivatives. XIII. The oxidation of 10-deacetylbaccatin III
Appendino, Giovanni; Fenoglio, Ivana; Cravotto, Giancarlo; Varese, Marcella; Gariboldi, Pierluigi; et al, Gazzetta Chimica Italiana, 1994, 124(6), 253-7
合成路线:1 步
反应条件:
参考文献:
Preparation and pharmaceutical composition of Δ12,13-isotaxol analogs for use as antineoplastic agents
, United States, , ,
合成路线:1 步
参考文献:
Semi-synthetic taxanes with anti-tumoral activity
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Modification of taxane A ring via maneuvering of the C-11 double bond of 10-deacetylbaccatin III to get novel rearranged taxoids
Chakraborty, Vaishali; Bordoloi, Manobjyoti, Letters in Organic Chemistry, 2008, 5(8), 687-691