1. GPCR/G Protein
  2. Guanylate Cyclase
  3. Avenciguat

Avenciguat (BI-685509) is a potent and orally active sGC activator. Avenciguat restores cyclic guanosine monophosphate (cGMP) and improves functionality of nitric oxide (NO) pathways. Avenciguat can be used in research of chronic kidney disease (CKD) and diabetic kidney disease (DKD).

For research use only. We do not sell to patients.

Avenciguat

Avenciguat Chemical Structure

CAS No. : 1579514-06-9

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Description

Avenciguat (BI-685509) is a potent and orally active sGC activator. Avenciguat restores cyclic guanosine monophosphate (cGMP) and improves functionality of nitric oxide (NO) pathways. Avenciguat can be used in research of chronic kidney disease (CKD) and diabetic kidney disease (DKD)[1].

In Vitro

Avenciguat increased cGMP in human and rat platelet-rich plasma treated with the heme-oxidant ODQ.html" class="link-product" target="_blank">ODQ (HY-101255) with EC50 values are 467 nM and 304 nM, respectively[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Avenciguat (1, 3, 10, 30 mg/kg; p.o.) co-administered with Enalapril.html" class="link-product" target="_blank">Enalapril (HY-B0331) reduce proteinuria and incidence of glomerular sclerosis in a dose-dependent manner[1].
Avenciguat (30 mg/kg; p.o.) reduces tubulointerstitial fibrosis in rat unilateral ureteral obstruction (UUO) model[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: ZSF1 rat model[1]
Dosage: 1, 3, 10, 30 mg/kg; 3 mg/kg (enalapril)
Administration: Oral administration; daily
Result: Reduced proteinuria and incidence of glomerular sclerosis in a dose-dependent manner.
Animal Model: rat UUO model[1]
Dosage: 30 mg/kg
Administration: v
Result: Reduced tubulointerstitial fibrosis in rat UUO model.
Clinical Trial
Molecular Weight

582.69

Formula

C34H38N4O5

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

O=C(C1=C(OCC)N(C2=NC(C3=C(OCC4=CC=C5C(CCN(C6CCOCC6)C5)=C4C)C(C)=CC=C3)=CC=C2)N=C1)O

Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Solvent & Solubility
In Vitro: 

DMSO : 2 mg/mL (3.43 mM; ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.7162 mL 8.5809 mL 17.1618 mL
5 mM --- --- ---
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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Purity & Documentation
References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.7162 mL 8.5809 mL 17.1618 mL 42.9045 mL
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Avenciguat
Cat. No.:
HY-153092
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