¡¡ Bienvenidos a buscar productos químicos en chem960.com!
cryptotackieine | 114414-78-7
Nombre del producto:cryptotackieine
Número CAS:114414-78-7
MF:C16H12N2
CID:177315
PubChem ID:390526
Investigación
Oferta
Productos relacionados
Nombre e identificación
- 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
- 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
Propiedades químicas y físicas
Atributos calculados
- Calidad precisa: 232.100048391g/mol
- Recuento de donantes vinculados al hidrógeno: 0
- Recuento de receptores de enlace de hidrógeno: 1
- Cuenta de enlace giratorio: 0
- Masa isotópica única: 232.100048391g/mol
- Recuento de átomos pesados: 18
- Complejidad: 316
- Recuento atómico isotópico: 0
- Recuento del Centro estereoscópico atómico definido: 0
- Recuento de centros estereoscópicos atómicos indefinidos: 0
- Recuento de centros tridimensionales de bonos fijos: 0
- Conteo indefinido de centros tridimensionales de Bond: 0
- Recuento de unidades de unión covalente: 1
- Xlogp3: 3.7
- Superficie del Polo topológico: 17.8
Letteratura correlata
- 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
Investigación