Product name：cryptotackieine

Computed Properties

• Exact Mass: 232.100048391g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Monoisotopic Mass: 232.100048391g/mol
• Heavy Atom Count: 18
• Complexity: 316
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count : 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• Covalently-Bonded Unit Count: 1
• XLogP3: 3.7
• Topological Polar Surface Area: 17.8

• 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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