Structure of BAY 41-2272
CAS No.: 256376-24-6
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
BAY 41-2272 is an activator of guanylate cyclases (sGC).
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Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
CAS No. : | 256376-24-6 |
Formula : | C20H17FN6 |
M.W : | 360.39 |
SMILES Code : | NC1=NC(C2=NN(CC3=CC=CC=C3F)C4=NC=CC=C42)=NC=C1C5CC5 |
MDL No. : | MFCD06411391 |
InChI Key : | ATOAHNRJAXSBOR-UHFFFAOYSA-N |
Pubchem ID : | 9798973 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
Description |
BAY 41-2272, an oral and soluble activator of guanylate cyclases (sGC), enhances sGC activity 400-fold in combination with NO. It effectively reduces cardiac workload and boosts cardiac output, making it suitable for cardiovascular disease research[1][2].
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In Vitro:
Cell Line
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Concentration | Treated Time | Description | References |
msGC-NT (truncated Manduca sexta sGC) | 5 µM | To investigate the effect of BAY 41-2272 on the heme pocket of sGC. The results showed that upon binding of BAY 41-2272, a new fast phase appeared during CO photolysis, indicating that CO molecules were trapped and recaptured in the heme pocket | J Am Chem Soc. 2008 Nov 26;130(47):15748-9 | |
UM47 cells | 10 μM | 72 h | significantly reduced clonogenic survival | Cancer Lett. 2016 Jan 28;370(2):279-85 |
CAL27 cells | 10 μM | 72 h | significantly increased apoptosis | Cancer Lett. 2016 Jan 28;370(2):279-85 |
CAL27 cells | 10 μM | 24 h | significantly decreased cell proliferation | Cancer Lett. 2016 Jan 28;370(2):279-85 |
CAL27 cells | 10 μM | 72 h | decreased cell viability, induced apoptosis | Cancer Lett. 2016 Jan 28;370(2):279-85 |
human lung slices (PCLS) | 10, 20, or 50 μM | 30 min | To test the bronchodilatory effect of BAY 41-2272 in human lung slices, results showed that BAY 41-2272 could dilate preconstricted small airways. | Proc Natl Acad Sci U S A. 2016 Apr 26;113(17):E2355-62 |
Platelets | 10 μM | 10 min | To evaluate the effect of BAY 41-2272 on thrombin-induced P-selectin expression in platelets. Results showed that BAY 41-2272 significantly reversed thrombin-induced P-selectin expression. | Proc Natl Acad Sci U S A. 2004 Feb 3;101(5):1386-91 |
Human umbilical vein endothelial cells (HUVECs) | 10 μM | 30 min to 5 h | To evaluate the effect of BAY 41-2272 on IL-1β-induced P-selectin expression. Results showed that BAY 41-2272 significantly attenuated IL-1β-induced P-selectin expression but had no effect on E-selectin and ICAM-1 expression. | Proc Natl Acad Sci U S A. 2004 Feb 3;101(5):1386-91 |
Human embryonic stem cells (H-9) | 1-9 μM | 24 h | To investigate the effect of BAY 41-2272 on the differentiation of human embryonic stem cells into myocardial cells, showing a dose-dependent increase in Nkx2.5 mRNA expression. | Proc Natl Acad Sci U S A. 2008 Dec 2;105(48):18924-9 |
Mouse embryonic stem cells (EZ1) | 1-3 μM | 8 days | To investigate the effect of BAY 41-2272 on the differentiation of mouse embryonic stem cells into myocardial cells, showing a 65% to 2-fold increase in Nkx2.5 mRNA expression. | Proc Natl Acad Sci U S A. 2008 Dec 2;105(48):18924-9 |
CAL27 cells | 10 μM | 60 min | increased intracellular cGMP content, significantly higher than control | Cancer Lett. 2016 Jan 28;370(2):279-85 |
Washed platelets | 10 μM | 3 min | To evaluate the inhibitory effect of BAY 41-2272 on platelet aggregation and its impact on cGMP levels. Results showed that BAY 41-2272 significantly inhibited platelet aggregation and increased cGMP levels. | Cardiovasc Diabetol. 2012 Jan 16;11:5 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
Lambs | Acute pulmonary hypertension model | Inhalation | 0.05, 0.1, and 0.15 mg/kg | 2-hour intervals between each dose | Inhalation of BAY 41-2272 produced dose-dependent pulmonary vasodilation and increased transpulmonary cGMP release without significant effect on mean arterial pressure. | Am J Respir Crit Care Med. 2007 Dec 1;176(11):1138-45 |
Mice | Ovalbumin (OVA) and house dust mite extract (HDME)-induced allergic asthma models | Intratracheal administration | 30 μg/kg | Single dose, 30 minutes before testing | To test the bronchodilatory effect of BAY 41-2272 in allergic asthma mouse models, results showed that BAY 41-2272 could significantly reduce or eliminate airway hyperresponsiveness. | Proc Natl Acad Sci U S A. 2016 Apr 26;113(17):E2355-62 |
Mice | ENOS knockout and wild-type mice | Tissue superfusion | 0.3-1 μM | Single administration, observation time not specified | To evaluate the effect of BAY 41-2272 on leukocyte rolling and adhesion. Results showed that BAY 41-2272 significantly reduced leukocyte rolling and adhesion in eNOS knockout mice to levels observed in WT animals. Additionally, BAY 41-2272 inhibited IL-1β-induced leukocyte rolling and adhesion. | Proc Natl Acad Sci U S A. 2004 Feb 3;101(5):1386-91 |
Tags: BAY 41-2272 | BAY 41-2272 | soluble guanylate cyclase activator | sGC stimulator | nitric oxide (NO) signaling pathway enhancer | cyclic GMP (cGMP) pathway modulator | vasodilation inducer | cardiovascular therapeutic agent | pulmonary hypertension research compound | blood pressure regulator | endothelial function enhancer | heme-dependent sGC agonist | smooth muscle relaxation promoter | vascular tone modulator | nitric oxide-independent sGC activator | NO–sGC–cGMP signaling cascade | oxidative stress-sensitive target | pro-angiogenic signaling | 256376-24-6 |
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H250 | Catches fire spontaneously if exposed to air |
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