104713-40-8 Usage
Molecular structure
A complex synthetic compound with an indole-2-carboxamide backbone, a tetrahydro-7-methyl-4-oxocyclopropa(C)pyrrolo(3,2-e)indol-2(1H)-yl group, and an indol-5-yl group.
Chirality
A racemic mixture (+-) with equal amounts of both enantiomers.
Potential applications
May have potential in pharmaceutical research due to unique structure and biological activities associated with indole derivatives.
Check Digit Verification of cas no
The CAS Registry Mumber 104713-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,1 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 104713-40:
(8*1)+(7*0)+(6*4)+(5*7)+(4*1)+(3*3)+(2*4)+(1*0)=88
88 % 10 = 8
So 104713-40-8 is a valid CAS Registry Number.
InChI:InChI=1/C30H23N5O3/c1-15-13-31-27-24(36)11-25-30(26(15)27)12-18(30)14-35(25)29(38)23-10-17-8-19(6-7-21(17)34-23)32-28(37)22-9-16-4-2-3-5-20(16)33-22/h2-11,13,18,31,33-34H,12,14H2,1H3,(H,32,37)
104713-40-8Relevant academic research and scientific papers
Stereoelectronic factors influencing the biological activity and DNA interaction of synthetic antitumor agents modeled on CC-1065
Warpehoski,Gebhard,Kelly,Krueger,Li,McGovren,Prairie,Wicnienski,Wierenga
, p. 590 - 603 (2007/10/02)
The synthesis, physicochemical properties, and biological activities of a series of novel spiro cyclopropyl compounds, modeled on the potent antitumor antibiotic CC-1065 (1), are described. Many of these synthetic analogues are significantly more effectiv
