GS-9620 - ≥95% , Toll-like receptor 7 activator, CAS No.1228585-88-3, Toll-like receptor 7 activator

CAS: 1228585-88-3 Cat. No.: G126483 Formula: C22H30N6O2 Peso molecolare: 410.51
Disponibile su ordine
GRADE & PURITY ≥95%
Synonyms
Vesatolimod [USAN:INN] | BDBM50440284 | Vesatolimod | VFOKSTCIRGDTBR-UHFFFAOYSA-N | MFCD25372045 | AKOS025290740 | AMY41043 | CCG-268776 | FT-0721305 | Vesatolimod [INN] | VESATOLIMOD [USAN] | BCP08305 | 8-(3-(pyrrolidin-1-ylmethyl)benzyl)-4-amino-2-butox
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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Size
Germania (EU)
USA*
Price
Qty
5mg
G126483-5mg
—
3 Disponibile
46,77€
10mg
G126483-10mg
—
3 Disponibile
73,67€
50mg
G126483-50mg
—
2 Disponibile
306,23€
100mg
G126483-100mg
—
2 Disponibile
609,07€
Enter a quantity for the sizes you want to add.
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Why this grade

≥95% 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.

Panoramica

product description:

GS-9620 is an effective and specific orally active agonist of Toll-like receptor 7.

In vitro activity:

GS-9620 rapidly internalizes into cells and preferentially localizes to and signals from endo-lysosomal compartments. To test this hypothesis, the kinetics of cellular uptake of the compound in Daudi cells using tritiated GS-9620 (3H-GS-9620) is measured. The kinetics of 3H-GS-9620 accumulation is rapid, reaching concentration-dependent steady-state equilibrium in approximately thirty minutes. Measured intracellular concentration of 3H-GS-9620 is 5-fold higher than the extracellular concentration of 3H-GS-9620 used to treat cells. Increases in intracellular 3H-GS-9620 concentrations are roughly proportional with increasing concentrations of 3H-GS-9620

In vivo activity

Single oral doses of GS-9620 at 0.3 and 1 mg/kg in uninfected chimpanzees demonstrates a dose- and exposure-related induction of serum IFN-α, select cytokines/chemokines, and interferon-stimulated genes (ISG) in the peripheral blood and liver. Following oral administration at 0.3 (n=3), and 1 mg/kg (n=3 and n=4), GS-9620 Cmax is 3.6±3.5, 36.8±34.5, and 55.4±81.0 nM, respectively. Peak serum interferon responses occur at 8 h post-dose. The mean peak levels of induced serum IFN-α are 66 and 479 pg/mL at doses of 0.3 and 1 mg/kg, respectively. GS-9620 treatment induces ISG transcripts including ISG15, OAS-1, MX1, IP-10 (CXCL10), and I-TAC (CXCL11) in peripheral blood mononuclear cells (PBMC) at 0.3 mg/kg and in both PBMC and the liver at 1 mg/kg.


Specifications

Sinonimi
Vesatolimod [USAN:INN] | BDBM50440284 | Vesatolimod | VFOKSTCIRGDTBR-UHFFFAOYSA-N | MFCD25372045 | AKOS025290740 | AMY41043 | CCG-268776 | FT-0721305 | Vesatolimod [INN] | VESATOLIMOD [USAN] | BCP08305 | 8-(3-(pyrrolidin-1-ylmethyl)benzyl)-4-amino-2-butox
Specifiche e purezza
≥95%
Meccanismi biochimici e fisiologici

Description: IC50 Value: N/A GS-9620 is a potent and selective orally active small molecule agonist of Toll-like receptor 7(TLR-7) in chimpanzees with chronic HBV infection [1]. GS-9620 is a novel oral agonist of Toll-like receptor 7 (TLR

Condizioni di conservazione di stoccaggio
Store at -20°C
Spedito in
Ice chest + Ice pads
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Tipo di azione
ACTIVATOR
Meccanismo d'azione
Toll-like receptor 7 activator
Purezza
≥95%
Proprietà del prodotto
ALogP2.7
Nomi e identificatori
Pubchem Sid504770702
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504770702
Sorrisi canoniciCCCCOC1=NC(=C2C(=N1)N(CC(=O)N2)CC3=CC=CC(=C3)CN4CCCC4)N
IUPAC Name4-amino-2-butoxy-8-[[3-(pyrrolidin-1-ylmethyl)phenyl]methyl]-5,7-dihydropteridin-6-one
InChIKeyVFOKSTCIRGDTBR-UHFFFAOYSA-N
INCHI1S/C22H30N6O2/c1-2-3-11-30-22-25-20(23)19-21(26-22)28(15-18(29)24-19)14-17-8-6-7-16(12-17)13-27-9-4-5-10-27/h6-8,12H,2-5,9-11,13-15H2,1H3,(H,24,29)(H2,23,25,26)
Isomeri SMILES CCCCOC1=NC(=C2C(=N1)N(CC(=O)N2)CC3=CC=CC(=C3)CN4CCCC4)N
Peso molecolare 410.51
Reaxy-Rn 20308598
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=20308598&ln=

Documentazione

📋 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
ClassePteridines and derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPteridines and derivatives
Alternative Parents Alpha amino acids and derivatives  Phenylmethylamines  Dialkylarylamines  Benzylamines  Alkyl aryl ethers  Aminopyrimidines and derivatives  Aralkylamines  N-alkylpyrrolidines  Imidolactams  Heteroaromatic compounds  Trialkylamines  Secondary carboxylic acid amides  Lactams  Azacyclic compounds  Carbonyl compounds  Hydrocarbon derivatives  Organic oxides  Primary amines  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Alpha-amino acid or derivatives - Pteridine - Benzylamine - Phenylmethylamine - Dialkylarylamine - Alkyl aryl ether - Aminopyrimidine - Aralkylamine - Monocyclic benzene moiety - Pyrimidine - N-alkylpyrrolidine - Benzenoid - Imidolactam - Pyrrolidine - Heteroaromatic compound - Secondary carboxylic acid amide - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Carboxamide group - Lactam - Azacycle - Carboxylic acid derivative - Ether - Organooxygen compound - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Primary amine - Organic oxide - Organic oxygen compound - Amine - Organonitrogen compound - Aromatic heteropolycyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as pteridines and derivatives. These are polycyclic aromatic compounds containing a pteridine moiety, which consists of a pyrimidine fused to a pyrazine ring to form pyrimido(4,5-b)pyrazine.
External Descriptors Not available
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
TLR7 Tclin Toll-like receptor 7 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TLR8 Tchem Toll-like receptor 8 (1853 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Liver microsomes (16955 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Liver (3974 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cynomolgus monkey (4946 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Tlr7 Toll-like receptor 7 (174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
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.

5 results found

Lot NumberCertificate TypeDataOggetto
I2620023Certificate of AnalysisSep 28, 2026 G126483
H2223124Certificate of AnalysisMar 11, 2026 G126483
H2223266Certificate of AnalysisMar 11, 2026 G126483
H2223267Certificate of AnalysisMar 11, 2026 G126483
H2223268Certificate of AnalysisMar 11, 2026 G126483
Proprietà chimiche e fisiche
SolubilitàDMSO mg/mL Water mg/mL Ethanol mg/mL
Peso molecolare410.500 g/mol
XLogP32.700
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count7
Rotatable Bond Count8
Exact Mass410.243 Da
Monoisotopic Mass410.243 Da
Topological Polar Surface Area96.600 Ų
Heavy Atom Count30
Formal Charge0
Complexity558.000
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
Domande frequenti e articoli
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

Domande frequenti

What is the purity of this product?
This product is supplied at ≥95% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.
How should this product be stored?
Store at ?20 °C. Freezer storage is required to maintain the specified shelf life.
How is this product shipped?
This product ships in an insulated container with ice pads. Unpack on arrival and transfer it to the storage condition stated above.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 1228585-88-3, the molecular formula is C22H30N6O2, and the molecular weight is 410.51 g/mol. InChIKey VFOKSTCIRGDTBR-UHFFFAOYSA-N.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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