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Home > Encyclopedia > 8-(4-Chlorophenylthio)-cGMP

8-(4-Chlorophenylthio)-cGMP

8-(4-Chlorophenylthio)-cGMP structure

8-(4-Chlorophenylthio)-cGMP 

structure
  • CAS No:

    54364-02-2

  • Formula:

    C16H15ClN5O7PS

  • Chemical Name:

    8-(4-Chlorophenylthio)-cGMP

  • Synonyms:

    Guanosine,8-[(4-chlorophenyl)thio]-,cyclic 3′,5′-(hydrogen phosphate);4H-Furo[3,2-d]-1,3,2-dioxaphosphorin,guanosine deriv.;8-(4-Chlorophenylthio)-cGMP;8-(p-Chlorophenylthio)-cGMP

  • Categories:

    Biochemical Engineering  >  Saccharides

Description

8-(4-chlorophenylthio)-cGMP is a 3',5'-cyclic purine nucleotide that is 3',5'-cyclic GMP 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, a ribonucleotide, an aryl sulfide and an organochlorine compound. It derives from a 3',5'-cyclic GMP. It is a conjugate acid of an 8-(4-chlorophenylthio)-cGMP(1-).

8-(4-Chlorophenylthio)-cGMP Basic Attributes

589.00100

487.81

Characteristics

213.16000

3.20980

2.19g/cm3

841.8ºC at 760 mmHg

462.9ºC

1.927

Drug Information

Drugs or agents which antagonize or impair any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system. (See all compounds classified as Platelet Aggregation Inhibitors.)

8-((4-chlorophenyl)thio)cyclic-3',5'-GMP

Computed Properties

Molecular Weight:487.8
XLogP3:-0.4
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:3
Exact Mass:487.0118337
Monoisotopic Mass:487.0118337
Topological Polar Surface Area:196
Heavy Atom Count:31
Complexity:817
Defined Atom Stereocenter Count:4
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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