471-68-1 (齐墩果酸-12-烯,Olean-12-ene)

快速询单

结构式：

齐墩果酸-12-烯MOL文件

CAS号：

471-68-1

中文名称：

齐墩果酸-12-烯

英文名称：

Olean-12-ene

分子式：

C₃₀H₅₀

分子量：

410.718009471893

植物源：

台湾裸实

齐墩果酸-12-烯(471-68-1)名称与标识符

名称

英文别名：

Olean-12-ene;18BETA(H)-OLEAN-12(13)-ENE;18ß(H)-OLEAN-12(13)-ENE;18ß(H)-Olean-12(13)-ene100µg;Olean-12-en;

标识符

InChIKey：

ZTLIRKGRXLVPOF-GAXUHWGVSA-N

Inchi：

1S/C30H50/c1-25(2)16-17-27(5)18-19-29(7)21(22(27)20-25)10-11-24-28(6)14-9-13-26(3,4)23(28)12-15-30(24,29)8/h10,22-24H,9,11-20H2,1-8H3/t22-,23-,24+,27+,28-,29+,30+/m0/s1

SMILES：

[C@@]12(C)CC[C@H]3C(C)(C)CCC[C@]3(C)[C@H]1CC=C1[C@@H]3CC(C)(C)CC[C@]3(C)CC[C@@]21C

齐墩果酸-12-烯(471-68-1)物化性质

实验特性

LogP : 9.19810
PSA : 0.00000

计算特性

精确分子量 : 410.39100

齐墩果酸-12-烯(471-68-1)推荐厂家更多厂家(1)

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齐墩果酸-12-烯(471-68-1)相关文献

1. The synthesis of β-amyrin
D. H. R. Barton,E. F. Lier,J. F. McGhie J. Chem. Soc. C 1968 1031
2. 279. Triterpenoids. Part XLVIII. Olean-13(18)-ene : isomerisation of olean-12-ene and related hydrocarbons with mineral acid
George Brownlie,M. B. E. Fayez,F. S. Spring,Robert Stevenson,W. S. Strachan J. Chem. Soc. 1956 1377
3. 170. Triterpenes of the friedelane series. Part III. The course of the friedelene–oleanene rearrangement
J. L. Courtney,R. M. Gascoigne,A. Z. Szumer J. Chem. Soc. 1958 881
4. Design, synthesis and biological evaluation of novel amide-linked 18β-glycyrrhetinic acid derivatives as novel ALK inhibitors
Dong Cai,Zhi hua Zhang,Yu Chen,Chao Ruan,Sheng qiang Li,Shi qin Chen,Lian shan Chen RSC Adv. 2020 10 11694
5. 3-(2,6-Dichloro-benzyloxy)-11-oxo-olean-12-ene-29-oic acid, a semisynthetic derivative of glycyrrhetic acid: synthesis, antiproliferative, apoptotic and anti-angiogenesis activity
Rajni Sharma,Santosh K. Guru,Shreyans K. Jain,Anup Singh Pathania,Ram A. Vishwakarma,Shashi Bhushan,Sandip B. Bharate Med. Chem. Commun. 2015 6 564
6. Triterpenoids. Part VIII. Allylic oxidation by N-bromosuccinimide
B. W. Finucane,J. B. Thomson J. Chem. Soc. Perkin Trans. 1 1972 1856
7. Barrigenol triterpenes from the husks of Xanthoceras sorbifolia Bunge and their antitumor activities
Da Wang,Dan Su,Xian-Zhe Li,Dan Liu,Rong-Gang Xi,Hui-Yuan Gao,Xiao-Bo Wang RSC Adv. 2016 6 27434
8. Network pharmacology-based study of the mechanisms of action of anti-diabetic triterpenoids from Cyclocarya paliurus
Zixin Lin,Yingpeng Tong,Na Li,Ziping Zhu,Junmin Li RSC Adv. 2020 10 37168
9. Stereochemistry at C-11 and C-12 in the biosynthesis of olean-12-ene, urs-12-ene, and β-sitosterol from [5-13C,5-2H2]mevalonolactone in tissue cultures of Isodon japonicus Hara
Shujiro Seo,Yutaka Tomita,Kazuo Tori,Yohko Yoshimura J. Chem. Soc. Chem. Commun. 1980 1275
10. Six new triterpenoids and other triterpenoids and steroids from three Quercus species of Hong Kong
Wai-Haan Hui,Man-Moon Li J. Chem. Soc. Perkin Trans. 1 1977 897