8-(4-Chlorophenylthio)-cAMP
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8-(4-Chlorophenylthio)-cAMP
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CAS No:
41941-66-6
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Formula:
C16H15ClN5O6PS
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Chemical Name:
8-(4-Chlorophenylthio)-cAMP
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Synonyms:
Adenosine,8-[(4-chlorophenyl)thio]-,cyclic 3′,5′-(hydrogen phosphate);4H-Furo[3,2-d]-1,3,2-dioxaphosphorin,adenosine deriv.;8-(p-Chlorophenylthio)adenosine 3′,5′-cyclic phosphate;8-(p-Chlorophenylthio) 3′,5′-cyclic AMP;8-(4-Chlorophenylthio)-cAMP;8-(p-Chlorophenylthio)-cAMP;8-(4-Chlorophenylthio)cyclic AMP;8-(p-Chlorophenylthio)-cyclic AMP;CPT;111750-89-1;72549-29-2
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CAS No:
Description
8-(4-chlorophenylthio)-cAMP is a 3',5'-cyclic purine nucleotide that is 3',5'-cyclic AMP in which the hydrogen at position 2 on the purine fragment is replaced by a 4-chlorophenylthio group. It has a role as a protein kinase agonist. It is a 3',5'-cyclic purine nucleotide, an adenyl ribonucleotide, an organochlorine compound and an aryl sulfide. It derives from a 3',5'-cyclic AMP.
Drug Information
Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction. (See all compounds classified as Enzyme Inhibitors.)|Drugs intended to prevent damage to the brain or spinal cord from ischemia, stroke, convulsions, or trauma. Some must be administered before the event, but others may be effective for some time after. They act by a variety of mechanisms, but often directly or indirectly minimize the damage produced by endogenous excitatory amino acids. (See all compounds classified as Neuroprotective Agents.)
8-((4-chlorophenyl)thio)cyclic-3',5'-AMP
Computed Properties
Molecular Weight:471.8
XLogP3:0.5
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:11
Rotatable Bond Count:3
Exact Mass:471.0169191
Monoisotopic Mass:471.0169191
Topological Polar Surface Area:180
Heavy Atom Count:30
Complexity:693
Defined Atom Stereocenter Count:4
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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