MRT67307 HCl - ≥98% , CAS No.1781882-89-0

CAS: 1781882-89-0 Cat. No.: M413883 Molecular Weight: 464.6 (free-base)
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
N-[3-[[5-cyclopropyl-2-[3-(morpholin-4-ylmethyl)anilino]pyrimidin-4-yl]amino]propyl]cyclobutanecarboxamide hydrochloride
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5mg
M413883-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$206.90

$240.90
Save $34.00 (14.11%)
25mg
M413883-25mg
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$794.90

$927.90
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100mg
M413883-100mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$1,825.90

$2,129.90
Save $304.00 (14.27%)
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Why this grade

≥98% 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.

📋

Quality documents

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

📚

Literature proof

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

Overview

Information

MRT67307 is a potent and dualIKKϵandTBK1inhibitor with IC50 of 160 and 19 nM, respectively. MRT67307 potently inhibitsULK1andULK2and blocksautophagy.


Targets

IKKϵ (Cell-free assay); TBK1 (Cell-free assay) 160 nM; 190 nM


In vitro

In macrophages, MRT67307 prevents the phosphorylation of IRF3 and the production of IFNβ. In wild-type MEFs, MRT67307 enhances the IL-1-stimulated phosphorylation of p105 at Ser933 and RelA at both Ser468 and Ser536, and also enhances IL-1-stimulated activation of NF-κB-dependent gene transcription. MRT67307 increases IL-10 production and suppresses proinflammatory cytokine production via a cAMP response element-Binding protein (CREB)-regulated transcriptional coactivator (CRTC) 3 Dependent Mechanism. In addition, MRT67307 inhibit ULK and block autophagy in MEF cells.


Cell Research(from reference)

Cell lines:MEFs and 293T cells 

Concentrations:10 μM 

Incubation Time:1 h 

Specifications

Synonyms
N-[3-[[5-cyclopropyl-2-[3-(morpholin-4-ylmethyl)anilino]pyrimidin-4-yl]amino]propyl]cyclobutanecarboxamide hydrochloride
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
MRT67307 is a potent and dual IKKϵ and TBK1 inhibitor with IC50 of 160 and 19 nM, respectively. MRT67307 potently inhibits ULK1 and ULK2 and blocks autophagy.
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
INHIBITOR
Purity
≥98%
Names and Identifiers
Alternate CAS CAS 2095432-39-4;1190378-57-4
Molecular Weight 464.6 (free-base)

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

Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
SolubilitySolubility (25°C) In vitro DMSO: 92 mg/mL warmed with 50ºC Water: bath Water: 92 mg/mL Ethanol: 92 mg/mL
Solution Calculators
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Customer Reviews

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