Guanylatecyclase (guanylylcyclase, GC) is a lyase enzyme. Guanylylcyclase is often part of the G protein signaling cascade that is activated by low intracellular calcium levels and inhibited by high intracellular calcium levels. In response to calcium levels, guanylylcyclase synthesizes cGMP from GTP. cGMP keeps cGMP-gated channels open, allowing for the entry of calcium into the cell. The guanylylcyclase activity is modulated by the calcium-binding guanylylcyclase activating proteins (GCAP1 and GCAP2). A key mechanism by which Ca2+ modulates phototransduction in rods involves the synthesis of cGMP by guanylylcyclase (GC), regulated by a pair of Ca2+-binding GuanylylCyclase Activating Proteins (GCAP1 and GCAP2). The second messenger cyclic guanosine monophosphate (cGMP) is generated by the heterodimeric α/β-heme protein soluble guanylatecyclase (sGC) upon activation by its endogenous ligand nitric oxide (NO). NO binds to the reduced prosthetic heme group bound to the β subunit. cGMP is a key mediator of the cardiovascular system and its effects lead to vasodilation, inhibition of smooth muscle proliferation, blockade of leukocyte infiltration and inhibition of platelet aggregation. Impairment of the cytoprotective NO/sGC/cGMP-signalling pathway is associated with the development of serious cardiovascular diseases such as hypertension or heart failure.


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Olinciguat

Olinciguat (IW-1701) is an oral guanylate cyclase (sGC) stimulator with concentration-dependent stimulation of sGC in purified rat and human enzyme assays and a whole cell assay[1].

  • CAS Number: 1628732-62-6
  • MF: C21H16F5N7O3
  • MW: 509.39
  • Catalog: Guanylate Cyclase
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

CFM 1571 hydrochloride

CFM 1571 hydrochloride is the stimulator of the nitric oxide receptor, soluble guanylate cyclase (sGC) with an EC50 and IC50 of 5.49 μM and 2.84 μM, respectively. Soluble guanylate cyclase (sGC) is a key signal-transduction enzyme activated by nitric oxide (NO). CFM 1571 (hydrochloride) (compound 32) has the potential for the research of cardiovascular and other diseases[1][2].

  • CAS Number: 1215548-30-3
  • MF: C23H29ClN4O3
  • MW: 444.954
  • Catalog: Guanylate Cyclase
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

Praliciguat

Praliciguat (IW-1973) is a potent and orally active soluble guanylate cyclase stimulator, enhances NO signaling, acts as a vasodilator. Praliciguat (IW-1973) stimulates sGC in HEK-293 cells with an EC50 of 197 nM[1].

  • CAS Number: 1628730-49-3
  • MF: C21H14F8N6O2
  • MW: 534.36
  • Catalog: Guanylate Cyclase
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

RQIKIWFQNRRMKWKK

DT-3 is a membrane-permeable protein kinase G Iα inhibitory peptide. DT-3 is a guanylyl cyclase? inhibitor and shows pharmacological blockade of the cGMP–PKG signalling[1].

  • CAS Number: 329306-46-9
  • MF: C104H168N34O20S
  • MW:
  • Catalog: Guanylate Cyclase
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

Cinaciguat

Cinaciguat is an activator of guanylate cyclase (sGC), and used for acute decompensated heart failure.

  • CAS Number: 329773-35-5
  • MF: C36H39NO5
  • MW: 565.699
  • Catalog: Guanylate Cyclase
  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 731.0±60.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 395.9±32.9 °C

Ebselen oxide

Ebselen oxide, the selenone analogue of Ebselen, covalently modifies diguanylate cyclase (DGC) to inhibit c-di-GMP-receptor interactions and reduces DGC activity. Ebselen oxide also inhibits alginate production (IC50=14 μM) by Pseudomonas aeruginosa. Ebselen oxide inhibits HDAC1, HDAC3, HDAC4, HDAC5, HDAC6, HDAC7, HDAC8, and HDAC9 (IC50 ranging from 0.2 to 4.7 μM)[1][2][3].

  • CAS Number: 104473-83-8
  • MF: C13H9NO2Se
  • MW: 290.176
  • Catalog: Guanylate Cyclase
  • Density: N/A
  • Boiling Point: 277.3±23.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 121.5±22.6 °C

Uroguanylin Topoisomer A (human) trifluoroacetate salt

Uroguanylin (human) is a natural ligand for the Guanylyl Cyclase (GCC) receptor expressed in metastatic colorectal cancer tumors. Uroguanylin (human) has anti-tumor actions in an animal model for human colon cancer[1][2].

  • CAS Number: 154525-25-4
  • MF: C64H102N18O26S4
  • MW: 1667.86000
  • Catalog: Guanylate Cyclase
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

BM121307

BM121307 is a guanylate cyclase activator that was in phase I development for the treatment of ischaemic heart disorders. The research has been discontinued.

  • CAS Number: 137213-91-3
  • MF: C8H14N2O4
  • MW: 202.20800
  • Catalog: Guanylate Cyclase
  • Density: 1.2g/cm3
  • Boiling Point: 378.8ºC at 760mmHg
  • Melting Point: N/A
  • Flash Point: 182.9ºC

Mosliciguat

Mosliciguat is a guanylate cyclase activator[1].

  • CAS Number: 2231749-54-3
  • MF: C41H36ClF3N2O5
  • MW: 729.18
  • Catalog: Guanylate Cyclase
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A