Vericiguat - Moligand™, ≥98% , Soluble guanylate cyclase activator, CAS No.1350653-20-1, Soluble guanylate cyclase activator

CAS: 1350653-20-1 Cat. No.: V414461 Peso molecular: 426.38 Número EC: 814-370-3 PubChem CID: 54674461
Disponible para pedir
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
Vericiguat [USAN] | methyl N-[4,6-diamino-2-[5-fluoro-1-[(2-fluorophenyl)methyl]pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-5-yl]carbamate | SB16806 | 1350653-20-1 | DS-2178 | VERICIGUAT [JAN] | WHO 9805 | D11051 | Vericiguat | AKOS025289795 | BCP18886 | Methyl
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
2mg
V414461-2mg
3
9,90US$
5mg
V414461-5mg
3
10,90US$
10mg
V414461-10mg
2

12,90US$

19,90US$
Guardar 7,00 US$ (35.18%)
25mg
V414461-25mg
2

27,90US$

41,90US$
Guardar 14,00 US$ (33.41%)
50mg
V414461-50mg
2

49,90US$

74,90US$
Guardar 25,00 US$ (33.38%)
100mg
V414461-100mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

85,90US$

128,90US$
Guardar 43,00 US$ (33.36%)
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Why this grade

Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Information

Vericiguat Vericiguat (BAY1021189, Verquvo) is a potent, orally available and soluble guanylate cyclase (sGC) stimulator.


Targets

sGC


In vitro

The stimulation of sGC by Vericiguat is examined with a recombinant CHO cell line overexpressing rat sGC. Vericiguat stimulates the sGC reporter cell line concentration dependently with an EC50 of 1005 ± 145 nM. In the presence of the NO donor S-nitroso-N-acetyl-D,L-penicillamine (SNAP) (30 and 100 nM), the EC50 value shifts to 39.0 ± 5.1 and 10.6 ± 1.7 nM, respectively. In the presence of ODQ, pretreatment of the sGC reporter cell line with 10 μM ODQ for 3 h results in a significantly reduced efficacy of Vericiguat, with an EC50 of 256 ± 40 nM being observed.


In vivo

Vericiguat can maintain heart and kidney function in a model of hypertension-induced end-organ damage with substantially reduced overall mortality.


Cell Research(from reference)

Cell lines:CHO cells 

Concentrations:0.01 μM to 100 μM 

Incubation Time:6 min 

Specifications

Sinónimos
Vericiguat [USAN] | methyl N-[4, 6-diamino-2-[5-fluoro-1-[(2-fluorophenyl)methyl]pyrazolo[3, 4-b]pyridin-3-yl]pyrimidin-5-yl]carbamate | SB16806 | 1350653-20-1 | DS-2178 | VERICIGUAT [JAN] | WHO 9805 | D11051 | Vericiguat | AKOS025289795 | BCP18886 | Methyl
Especificaciones y pureza
Moligand™, ≥98%
Mecanismos bioquímicos y fisiológicos
Vericiguat (BAY1021189, Verquvo) is a potent, orally available and soluble guanylate cyclase (sGC) stimulator.
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
Moligand™
Tipo de acción
ACTIVATOR
Mecanismo de acción
Soluble guanylate cyclase activator
Pureza
≥98%
Propiedades del producto
ALogP2.341
Recuento HBD3
Enlace rotable5
Nombres e identificadores
Pubchem Sid504771336
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504771336
Sonrisas canónicasCOC(=O)NC1=C(N=C(N=C1N)C2=NN(C3=C2C=C(C=N3)F)CC4=CC=CC=C4F)N
IUPAC Namemethyl N-[4,6-diamino-2-[5-fluoro-1-[(2-fluorophenyl)methyl]pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-5-yl]carbamate
InChIKeyQZFHIXARHDBPBY-UHFFFAOYSA-N
INCHI1S/C19H16F2N8O2/c1-31-19(30)25-14-15(22)26-17(27-16(14)23)13-11-6-10(20)7-24-18(11)29(28-13)8-9-4-2-3-5-12(9)21/h2-7H,8H2,1H3,(H,25,30)(H4,22,23,26,27)
Isómeros SMILES COC(=O)NC1=C(N=C(N=C1N)C2=NN(C3=C2C=C(C=N3)F)CC4=CC=CC=C4F)N
PubChem CID 54674461
Peso molecular 426.38

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasePyrazolopyridines
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPyrazolopyridines
Alternative Parents Fluorobenzenes  Aminopyrimidines and derivatives  Pyridines and derivatives  Imidolactams  Aryl fluorides  Pyrazoles  Heteroaromatic compounds  Carbamate esters  Azacyclic compounds  Primary amines  Organofluorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Pyrazolopyridine - Aminopyrimidine - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Imidolactam - Benzenoid - Pyrimidine - Pyridine - Monocyclic benzene moiety - Azole - Heteroaromatic compound - Carbamic acid ester - Pyrazole - Azacycle - Amine - Organofluoride - Organohalogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Primary amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as pyrazolopyridines. These are compounds containing a pyrazolopyridine skeleton, which consists of a pyrazole fused to a pyridine. Pyrazole is 5-membered ring consisting of three carbon atoms and two adjacent nitrogen centers. Pyridine is a 6-membered ring with four carbon and one nitrogen atoms.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
GUCY1A1 Tclin Guanylate cyclase soluble subunit alpha-1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GUCY1A2 Tclin Guanylate cyclase soluble subunit alpha-2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GUCY1B1 Tclin Guanylate cyclase soluble subunit beta-1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CYP2C8 Tchem Cytochrome P450 2C8 (1492 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2A6 Tchem Cytochrome P450 2A6 (2861 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2B6 Tchem Cytochrome P450 2B6 (1338 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Canis familiaris (36305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Artery (19 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Heart (171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aorta (2975 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Gucy1a1 Guanylate cyclase soluble subunit alpha-1 (85 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeFechaArticulo
F2210179Certificate of AnalysisMar 04, 2025 V414461
F2210195Certificate of AnalysisMar 04, 2025 V414461
F2210196Certificate of AnalysisMar 04, 2025 V414461
F2210197Certificate of AnalysisMar 04, 2025 V414461
F2210198Certificate of AnalysisMar 04, 2025 V414461
F2210199Certificate of AnalysisMar 04, 2025 V414461
F2210193Certificate of AnalysisMay 23, 2022 V414461
Propiedades químicas y físicas
SolubilidadSolubility (25°C) In vitro DMSO: 85 mg/mL (199.35 mM); Water: Insoluble; Ethanol: Insoluble;
DMSO (mg/ml) Solubilidad máxima85
DMSO (mM) Solubilidad máxima199.352690088653
Agua (mg/ml) Solubilidad máxima<1
Peso molecular426.400 g/mol
XLogP31.500
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count10
Rotatable Bond Count5
Exact Mass426.136 Da
Monoisotopic Mass426.136 Da
Topological Polar Surface Area147.000 Ų
Heavy Atom Count31
Formal Charge0
Complexity622.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Calculadoras de soluciones
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