TyK2-IN-2 - 10mM in DMSO , CAS No.2098466-94-3

CAS: 2098466-94-3 Cat. No.: T654529 Molecular Weight: 310.35 PubChem CID: 129626433
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GRADE & PURITY 10mM in DMSO
Storage
Store at -80°C
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1ml
T654529-1ml
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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.

Overview

TyK2-IN-2 (Compoud 18) is a potent and selective TYK2 inhibitor with IC 50 s of 7 nM, 0.1 μM and 0.05 μM for TYK2 JH2 , IL-23 and IFNα , respectively. TyK2-IN-2 also inhibits phosphodiesterase 4 (PDE4) with an IC 50 of 62 nM. TyK2-IN-2 can be used for the research of inflammatory and autoimmune diseases

In Vitro

A co-crystal structure of TyK2-IN-2 (Compoud 18) bound to the TYK2 JH2 is solved. First, limited room between C8 and the hinge is seen, consistent with the loss in affinity seen with groups larger than methylamino at this position. There are also hydrogen bonds revealed between the NH of the C8 methylamine and from N1 of the IZP core to the ‘hinge’ (Val690). Additional hydrogen bonds are observed from the oxygen of the C3 amide to Lys642 and to the hinge carbonyl of Glu688 through a bridging water molecule. The pocket proximal to the C3 amide of the TYK2 JH2 domain contains a combination of residues which are largely unique relative to the kinome such as a small residue (Ala671) under the “gatekeeper” (Thr687) and the replacement of the highly kinase-conserved DFG motif by DPG which alters the positioning of the conserved catalytic Lys642 and Asp759. The ability of the C3 amide to fit and bind to this pocket is believed to be a key source of kinome selectivity for TyK2-IN-2 (Compoud 18). MCE has not independently confirmed the accuracy of these methods. They are for reference only.

IC50& Target:Tyk2 JH2 7 nM (IC 50 ) PDE4 62 nM (IC 50 )

Specifications

Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
TyK2-IN-2 (Compoud 18) is a potent and selective TYK2 inhibitor with IC 50 s of 7 nM, 0.1 μM and 0.05 μM for TYK2 JH2 , IL-23 and IFNα , respectively. TyK2-IN-2 also inhibits phosphodiesterase 4 (PDE4) with an IC 50 of 62 nM. TyK2-IN-2 can be used for the
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers
Isomeric SMILES CC1=CC(=CC(=C1)NC2=NN3C(=CN=C3C(=C2)NC)C(=O)N)C
PubChem CID 129626433
Molecular Weight 310.35

Documentation

📋 Safety Data Sheet (SDS)

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

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✅ Certificate of Analysis (COA)

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

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Associated Targets(Human)
TYK2 Tclin Non-receptor tyrosine-protein kinase TYK2 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PDE4D Tclin cAMP-specific 3',5'-cyclic phosphodiesterase 4D (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Solution Calculators
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