114414-78-7
（新白叶藤碱,cryptotackieine）
新白叶藤碱
cryptotackieine
114414-78-7
C16H12N2
232.279883384705
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击：新白叶藤碱结构式
名称和标识符
| InChIKey |
PZIIKMBOSNKNFZ-UHFFFAOYSA-N |
| Inchi |
1S/C16H12N2/c1-18-15-9-5-2-6-11(15)10-13-12-7-3-4-8-14(12)17-16(13)18/h2-10H,1H3 |
| SMILES |
N1(C)C2=CC=CC=C2C=C2C3=CC=CC=C3N=C12 |
别名信息
- 中文别名 -
- 5-甲基吲哚[2,3-b]喹啉
- 新百叶藤碱
- 新百叶腾碱
- 新白叶藤碱
- 英文别名 -
- 5H-Quinindoline,5-methyl-
- 5-methylindolo[2,3-b]quinoline
- 5H-Quinindoline, 5-methyl-
- cryptotackieine
- 10.1021/np0496284
- 5H-Quinodoline, 5-methyl-
- 5-Methyl-5H-quinindoline
- NEOCRYPTOLEPINE
- NSC687967
- BDBM50412204
- 5-methyl-5h-indolo[2,3-b]quinoline
- NCI60_031751
- NCI60_031752
- CHEMBL115585
- DTXSID90150720
- CHEMBL465591
- EX-A5436
- SCHEMBL1833360
- 114414-78-7
- NSC-687967
- Cryptotackieine
- Neocryptolepine
- NSC 687967
物化性质
计算特性
| 精确分子量 |
232.100048391g/mol |
| 氢键供体数量 |
0 |
| 氢键受体数量 |
1 |
| 可旋转化学键数量 |
0 |
| 同位素质量 |
232.100048391g/mol |
| 重原子数量 |
18 |
| 复杂度 |
316 |
| 同位素原子数量 |
0 |
| 确定原子立构中心数量 |
0 |
| 不确定原子立构中心数量 |
0 |
| 确定化学键立构中心数量 |
0 |
| 不确定化学键立构中心数量 |
0 |
| 共价键单元数量 |
1 |
| 疏水参数计算参考值（XlogP） |
3.7 |
| 拓扑分子极性表面积 |
17.8 |
相关文献
-
1.
Advancements in the synthesis of fused tetracyclic quinoline derivatives
Ramadan A. Mekheimer,Mariam A. Al-Sheikh,Hanadi Y. Medrasi,Kamal U. Sadek RSC Adv. 2020 10 19867
-
2.
Studies on the Claisen rearrangements in the indolo[2,3-b]quinoline system
Nicholas Vo?te,Douglas Philp,Alexandra M. Z. Slawin,Nicholas J. Westwood Org. Biomol. Chem. 2010 8 442
-
3.
5-Methyl-N-(8-(5,6,7,8-tetrahydroacridin-9-ylamino)octyl)-5H-indolo[2,3-b]quinolin-11-amine: a highly potent human cholinesterase inhibitor
Li Wang,Ignacio Moraleda,Isabel Iriepa,Alejandro Romero,Francisco López-Mu?oz,Mourad Chioua,Tsutomu Inokuchi,Manuela Bartolini,José Marco-Contelles Med. Chem. Commun. 2017 8 1307
-
4.
An efficient iron-promoted synthesis of 6H-indolo[2,3-b]quinolines and neocryptolepine derivatives
Zicong Yan,Changfeng Wan,Jianyong Wan,Zhiyong Wang Org. Biomol. Chem. 2016 14 4405
-
5.
A Pd(ii)-catalyzed C–H activation approach to densely functionalized N-heteroaromatics related to neocryptolepine and their evaluation as potential inducers of apoptosis
Rajnikanth Sunke,Vimal Kumar,Mohd Ashraf Ashfaq,Swapna Yellanki,Raghavender Medisetti,Pushkar Kulkarni,E. V. Venkat Shivaji Ramarao,Nasreen Z. Ehtesham,Manojit Pal RSC Adv. 2015 5 44722
-
6.
Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid
Elida N. Thobokholt,Enrique L. Larghi,Andrea B. J. Bracca,Teodoro S. Kaufman RSC Adv. 2020 10 18978
-
7.
Baylis–Hillman acetates in organic synthesis: convenient one-pot synthesis of α-carboline framework – a concise synthesis of neocryptolepine
Deevi Basavaiah,Daggula Mallikarjuna Reddy Org. Biomol. Chem. 2012 10 8774
-
8.
Baylis–Hillman acetates in organic synthesis: convenient one-pot synthesis of α-carboline framework – a concise synthesis of neocryptolepine
Deevi Basavaiah,Daggula Mallikarjuna Reddy Org. Biomol. Chem. 2012 10 8774
-
9.
Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
Satoshi Hibino,Tominari Choshi Nat. Prod. Rep. 2001 18 66
-
10.
Simple synthesis 11-substituted norcryptotackieine derivatives
Micha? Nowacki,Krzysztof Wojciechowski RSC Adv. 2015 5 94296
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