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Motolimod (VTX-2337) - 99%, high purity , Toll-like receptor 8 agonist, CAS No.926927-61-9, Toll-like receptor 8 agonist

In stock
Item Number
M413715
Grouped product items
SKU Size
Availability
Price Qty
M413715-1mg
1mg
3
$35.90
M413715-5mg
5mg
3
$147.90
M413715-25mg
25mg
3
$484.90

TLR Agonists

Basic Description

Synonyms 2-amino-N,N-dipropyl-8-[4-(pyrrolidine-1-carbonyl)phenyl]-3H-1-benzazepine-4-carboxamide | 3H-1-Benzazepine-4-carboxamide, 2-amino-n,N-dipropyl-8-(4-(1-pyrrolidinylcarbonyl)phenyl)- | AKOS027422467 | EX-A1102 | GTPL9026 | D10716 | MOTOLIMOD [USAN] | s7161
Specifications & Purity Moligand™, ≥99%
Biochemical and Physiological Mechanisms Motolimod (VTX-2337) is a selective and potent Toll-like receptor 8 (TLR8) agonist with EC50 of 100 nM, > 50-fold selectivity over TLR7. Phase 2.
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade Moligand™
Action Type AGONIST
Mechanism of action Toll-like receptor 8 agonist
Product Description

Information

Motolimod (VTX-2337) Motolimod (VTX-2337) is a selective and potent Toll-like receptor 8 (TLR8) agonist with EC50 of 100 nM, > 50-fold selectivity over TLR7. Phase 2.


Targets

TLR8 100 nM(EC50)


In vitro

VTX-2337 stimulates the production of both TNFα with EC50 of 140 nM and IL-12 with EC50 of 120 nM in PBMCs. In monocytes and mDCs, VTX-2337 selectively induces the production of TNFα and IL-12 via NF-κB activation. VTX-2337 also stimulates IFNγ production from NK cells, augments the lytic function of NK cells and enhances ADCC.


In vivo

In an ovarian cancer mouse model, TX-2337 enhances the effect of pegylated liposomal doxorubicin (PLD).


Cell Research(from reference)

Cell lines:PBMCs or purified NK cells 

Concentrations:~500 nM 

Incubation Time:48 h 

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Benzazepines
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Benzazepines
Alternative Parents Benzamides  N-acylpyrrolidines  Benzoyl derivatives  Azepines  Imidolactams  Tertiary carboxylic acid amides  Propargyl-type 1,3-dipolar organic compounds  Carboxamidines  Azacyclic compounds  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Benzazepine - Benzamide - Benzoic acid or derivatives - Benzoyl - N-acylpyrrolidine - Azepine - Monocyclic benzene moiety - Imidolactam - Benzenoid - Tertiary carboxylic acid amide - Pyrrolidine - Carboxamide group - Amidine - Azacycle - Carboxylic acid amidine - Organic 1,3-dipolar compound - Carboxylic acid derivative - Propargyl-type 1,3-dipolar organic compound - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as benzazepines. These are organic compounds containing a benzene ring fused to an azepine ring (unsaturated seven-membered heterocycle with one nitrogen atom replacing a carbon atom).
External Descriptors Not available

Product Properties

ALogP 3.854
hba_count 3
HBD Count 1
Rotatable Bond 7

Associated Targets(Human)

TLR8 Tchem Toll-like receptor 8 (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
HepG2 (196354 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TLR8 Tchem Toll-like receptor 8 (1853 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Tlr7 Toll-like receptor 7 (174 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504768015
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504768015
IUPAC Name 2-amino-N,N-dipropyl-8-[4-(pyrrolidine-1-carbonyl)phenyl]-3H-1-benzazepine-4-carboxamide
INCHI InChI=1S/C28H34N4O2/c1-3-13-31(14-4-2)28(34)24-17-23-12-11-22(18-25(23)30-26(29)19-24)20-7-9-21(10-8-20)27(33)32-15-5-6-16-32/h7-12,17-18H,3-6,13-16,19H2,1-2H3,(H2,29,30)
InChIKey QSPOQCXMGPDIHI-UHFFFAOYSA-N
Smiles CCCN(CCC)C(=O)C1=CC2=C(C=C(C=C2)C3=CC=C(C=C3)C(=O)N4CCCC4)N=C(C1)N
Isomeric SMILES CCCN(CCC)C(=O)C1=CC2=C(C=C(C=C2)C3=CC=C(C=C3)C(=O)N4CCCC4)N=C(C1)N
Molecular Weight 458.6
Reaxy-Rn 12838053
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=12838053&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

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.

3 results found

Lot Number Certificate Type Date Item
G2219638 Certificate of Analysis May 09, 2025 M413715
G2219662 Certificate of Analysis May 09, 2025 M413715
G2219763 Certificate of Analysis May 09, 2025 M413715

Chemical and Physical Properties

Solubility Solubility (25°C) In vitro DMSO: 55 mg/mL warmed with 50ºC Water: bath (119.93 mM); Ethanol: 15 mg/mL (32.7 mM); Water: Insoluble;
DMSO(mg / mL) Max Solubility 55
DMSO(mM) Max Solubility 119.9302224
Water(mg / mL) Max Solubility <1
Molecular Weight 458.600 g/mol
XLogP3 3.800
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 7
Exact Mass 458.268 Da
Monoisotopic Mass 458.268 Da
Topological Polar Surface Area 79.000 Ų
Heavy Atom Count 34
Formal Charge 0
Complexity 771.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

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