Answer:
122
Step-by-step explanation:
Plug in 1 for x and 11 for y
1 to the power of any number will always equal 1
I hope this helps!
Answer:
Option 2
Step-by-step explanation:
¼Y - ½
= ¼Y - 2/4
= ¼(Y - 2)
Answer:
True. That is a function.
Step-by-step explanation:
A function just means that every input has only one output. The simpler way to do these is the vertical line test. Draw a vertical line anywhere on the graph and see if the vertical line is intersected in two places. If the vertical line is crossed twice, the graph isn't a function.
In parallelogram LMNO, NO = 10.2, and LO = 14.7. The basic property of a parallelogram that the opposite sides in a parallelogram are equal; so, two sides are 10.2 (NO=LM=10.2), and two sizes are 14.7, = (LO=MN=14.7).
The perimeter of the parallelogram LMNO is:
P= 2NO + 2LO.
P= (2 x 10.2)+(2 x 14.7).
P= 20.4 + 29.4.
So, P= 49.8.
Answer:The crystal structures of five 6-mercaptopurine derivatives, viz. 2-[(9-acetyl-9H-purin-6-yl)sulfanyl]-1-(3-methoxyphenyl)ethan-1-one (1), C16H14N4O3S, 2-[(9-acetyl-9H-purin-6-yl)sulfanyl]-1-(4-methoxyphenyl)ethan-1-one (2), C16H14N4O3S, 2-[(9-acetyl-9H-purin-6-yl)sulfanyl]-1-(4-chlorophenyl)ethan-1-one (3), C15H11ClN4O2S, 2-[(9-acetyl-9H-purin-6-yl)sulfanyl]-1-(4-bromophenyl)ethan-1-one (4), C15H11BrN4O2S, and 1-(3-methoxyphenyl)-2-[(9H-purin-6-yl)sulfanyl]ethan-1-one (5), C14H12N4O2S. Compounds (2), (3) and (4) are isomorphous and accordingly their molecular and supramolecular structures are similar. An analysis of the dihedral angles between the purine and exocyclic phenyl rings show that the molecules of (1) and (5) are essentially planar but that in the case of the three isomorphous compounds (2), (3) and (4), these rings are twisted by a dihedral angle of approximately 38°. With the exception of (1) all molecules are linked by weak C—H⋯O hydrogen bonds in their crystals. There is π–π stacking in all compounds. A Cambridge Structural Database search revealed the existence of 11 deposited compounds containing the 1-phenyl-2-sulfanylethanone scaffold; of these, only eight have a cyclic ring as substituent, the majority of these being heterocycles.
Keywords: crystal structure, mercaptopurines, supramolecular structure
Go to:
Chemical context
Purines, purine nucleosides and their analogs, are nitrogen-containing heterocycles ubiquitous in nature and present in biological systems like man, plants and marine organisms (Legraverend, 2008 ▸). These types of heterocycles take part of the core structure of guanine and adenine in nucleic acids (DNA and RNA) being involved in diverse in vivo catabolic and anabolic metabolic pathways.
6-Mercaptopurine is a water insoluble purine analogue, which attracted attention due to its antitumor and immunosuppressive properties. The drug is used, among others, in the treatment of rheumathologic disorders, cancer and prevent
Step-by-step explanation:
