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Chemical Structure| 41443-28-1 Chemical Structure| 41443-28-1

Structure of ODQ
CAS No.: 41443-28-1

Chemical Structure| 41443-28-1

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ODQ is a selective and irreversible inhibitor of nitric oxide-sensitive guanylyl cyclase.

Synonyms: 1H-ODQ

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Product Details of ODQ

CAS No. :41443-28-1
Formula : C9H5N3O2
M.W : 187.15
SMILES Code : O=C1ON=C2N1C3=C(C=CC=C3)N=C2
Synonyms :
1H-ODQ
MDL No. :MFCD00792620
InChI Key :LZMHWZHOZLVYDL-UHFFFAOYSA-N
Pubchem ID :1456

Safety of ODQ

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Related Pathways of ODQ

GPCR

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
DU-145 cells 50 µM 48 hours ODQ activated caspase-3 at 50 μM, promoting apoptosis. Br J Pharmacol. 2008 Nov;155(6):804-13
PC-3 cells 50 µM 48 hours ODQ activated caspase-3 at 50 μM, promoting apoptosis. Br J Pharmacol. 2008 Nov;155(6):804-13
Human platelets 10 µM 10 min ODQ inhibited VASP phosphorylation, but after prolonged incubation (3 min or longer) with NO donor, VASP phosphorylation signals recovered. Br J Pharmacol. 2013 Sep;170(2):317-27
Murine platelets 10 µM 10 min ODQ reduced NO-induced cGMP increases, but at high NO donor concentrations (100 μM DEA-NO), ODQ lost its inhibitory effect. Br J Pharmacol. 2013 Sep;170(2):317-27
HEK-GC cells 1, 10, 100 µM 10 min ODQ reduced NO-induced cGMP increases, but even at a concentration of 100 μM ODQ the NO-induced cGMP production was not completely abrogated. Br J Pharmacol. 2013 Sep;170(2):317-27
Cytosolic extracts from aortic rings and cardiomyocytes 50 µM 10 minutes To investigate the effects of ODQ on SNAP-induced increases in cGMP levels. In cytosolic extracts, ODQ reduced these effects by about 50%. Br J Pharmacol. 1999 Jun;127(3):693-700
Rat ventricular cardiomyocytes 50 µM 10 minutes To investigate the effects of ODQ on SNAP-, DETA NONOate-, and carbachol-induced increases in cGMP levels. In cardiomyocytes, ODQ did not affect these effects. Br J Pharmacol. 1999 Jun;127(3):693-700
Rat aortic rings 50 µM 10 minutes To investigate the effects of ODQ on SNAP-, DETA NONOate-, and carbachol-induced increases in cGMP levels. In aortic rings, ODQ completely abolished these effects. Br J Pharmacol. 1999 Jun;127(3):693-700
Rat coronary arteries 5 µM 20 minutes To investigate the effect of ODQ on dapagliflozin-induced vasodilation, results showed that ODQ did not affect dapagliflozin-induced vasodilation. Int J Mol Sci. 2023 Nov 28;24(23):16873
HEK293 cells 10 µM 30 minutes Measure intracellular cGMP levels, ODQ inhibited the effects of VL-102 and YC-1. Cephalalgia. 2018 Jul;38(8):1471-1484
Normal human prostate epithelial cells (HPrECs) 10 µM 48 hours ODQ at 10 μM did not activate caspase-3, indicating no apoptotic effect on normal cells. Br J Pharmacol. 2008 Nov;155(6):804-13
LNCaP cells 0.1 µM to 100 µM 48 hours ODQ activated caspase-3 at 50 and 100 μM, promoting apoptosis, and caused DNA fragmentation and nucleosome accumulation at 100 μM. Br J Pharmacol. 2008 Nov;155(6):804-13

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
C57BL6/J mice Chronic nitroglycerin migraine model Intraperitoneal injection 1 mg/kg Every other day for 9 days ODQ completely blocked acute and chronic hyperalgesia induced by nitroglycerin. Cephalalgia. 2018 Jul;38(8):1471-1484

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

5.34mL

1.07mL

0.53mL

26.72mL

5.34mL

2.67mL

53.43mL

10.69mL

5.34mL

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