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dipalmitoyl cyclic guanosinemonophosphate
Also Known As:
dihexadecanoyl cGMP; dihexadecanoyl-cyclic GMP; dipalmitoyl cGMP; dipalmitoyl-cyclic GMP; dp cGMP
Networked:
1
relevant articles (
0
outcomes,
0
trials/studies)
Bio-Agent Context: Research Results
Heterocyclic Compounds: 198
Fused-Ring Heterocyclic Compounds
2-Ring Heterocyclic Compounds
Purines: 651
Purine Nucleotides: 140
Guanine Nucleotides: 675
Cyclic GMP: 803
dipalmitoyl cyclic guanosinemonophosphate: 1
Nucleic Acids, Nucleotides, and Nucleosides: 1
Nucleotides: 15763
Cyclic Nucleotides: 1456
Cyclic GMP: 803
dipalmitoyl cyclic guanosinemonophosphate: 1
Ribonucleotides: 307
Guanine Nucleotides: 675
Cyclic GMP: 803
dipalmitoyl cyclic guanosinemonophosphate: 1
Purine Nucleotides: 140
Guanine Nucleotides: 675
Cyclic GMP: 803
dipalmitoyl cyclic guanosinemonophosphate: 1
Lipids: 114793
Fatty Acids: 27405
Palmitic Acids: 35
Palmitates: 1597
dipalmitoyl cyclic guanosinemonophosphate: 1
Related Diseases
1.
Lordosis
11/01/1983 - "
Lordosis behavior elicited with 2.0 mg/rat dp cGMP was blocked with 8.0 mg/rat methyl-isobutylxanthine (MIX), a phosphodiesterase inhibitor, suggesting that dp cGMP stimulated lordosis through its conversion to 5'GMP.
"
11/01/1983 - "
Dp cGMP and 5'GMP (2.0 mg/rat), also induced lordosis behavior in ovariectomized, adrenalectomized estrogen primed rats.
"
11/01/1983 - "
Free cGMP (2.0 mg/rat); dp cGMP (1.0, 2.0 and 4.0 mg/rat) and 5'GMP (2.0 and 4.0 mg/rat) induced significant lordosis behavior in ovariectomized, estrogen-primed rats.
"
11/01/1983 - "
The effect of systemic administration of guanosine, cGMP, dipalmitoyl (dp) cGMP, 5'GMP and 5'GDP on lordosis behavior was studied in ovariectomized, estradiol benzoate (EB) primed rats (4 micrograms/rat).
"
Related Drugs and Biologics
1.
Phosphodiesterase Inhibitors
2.
Guanosine Diphosphate (GDP)
3.
Guanosine
4.
Estrogens (Estrogen)
5.
estradiol 3-benzoate (estradiol benzoate)