JH-RE-06 - ≥98% , CAS No.1361227-90-8

CAS: 1361227-90-8 Cat. No.: J414220 Molecular Weight: 468.72
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
4(1H)​-​Quinolinone,8-​chloro-​2-​[(2,​4-​dichlorophenyl)​amino]​-​3-​(3-​methyl-​1-​oxobutyl)​-​5-​nitro- | 8-Chloro-2-[(2,4-dichlorophenyl)amino]-3-(3-methyl-1-oxobutyl)-5-nitro-4(1H)-quinolinone
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1mg
J414220-1mg
3
$59.90
5mg
J414220-5mg
2
$209.90
25mg
J414220-25mg
2
$739.90
50mg
J414220-50mg
2
$1,279.90
100mg
J414220-100mg
1
$2,059.90
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Why this grade

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

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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.

Overview

Information

JH-RE-06 JH-RE-06 is a potent REV1-REV7 interface inhibitor with an IC50 of 0.78 μM and Kd value of 0.42 μM, disrupting REV1-POL ζ-mediated mutagenic translesion synthesis (TLS).


Targets

REV1-REV7 (Cell-free assay); REV1-REV7 (Cell-free assay) 0.42 μM(Kd); 0.78 μM


In vitro

JH-RE-06 disrupts mutagenic TLS by preventing recruitment of mutagenic POL ζ. Remarkably, JH-RE-06 targets a nearly featureless surface of REV1 that interacts with the REV7 subunit of POL ζ. Binding of JH-RE-06 induces REV1 dimerization, which blocks the REV1-REV7 interaction and POL ζ recruitment. JH-RE-06 inhibits mutagenic TLS and enhances cisplatin-induced-toxicity in cultured human and mouse cell lines.


In vivo

JH-RE-06 improves tumor cell response to cisplatin in vivo. Co-administration of JH-RE-06 with cisplatin suppresses the growth of xenograft human melanomas in mice, establishing a framework for developing TLS inhibitors as a novel class of chemotherapy adjuvants.


Cell Research(from reference)

Cell lines:HT1080 cells, A375 cells, KP cells, MEF, LNCap cells, AG01522 cells. 

Concentrations:1.5 μM 

Incubation Time:24 h 

Specifications

Synonyms
4(1H)​-​Quinolinone, 8-​chloro-​2-​[(2, ​4-​dichlorophenyl)​amino]​-​3-​(3-​methyl-​1-​oxobutyl)​-​5-​nitro- | 8-Chloro-2-[(2, 4-dichlorophenyl)amino]-3-(3-methyl-1-oxobutyl)-5-nitro-4(1H)-quinolinone
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
JH-RE-06 is a potent REV1-REV7 interface inhibitor with an IC50 of 0.78 μM and Kd value of 0.42 μM, disrupting REV1-POL ζ-mediated mutagenic translesion synthesis (TLS).
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.
Purity
≥98%
Product Properties
ALogP6.232
hba_count2
HBD Count2
Rotatable Bond6
Names and Identifiers
Canonical SmilesCC(C)CC(=O)C1=C(NC2=CC=C(Cl)C=C2Cl)NC3=C(Cl)C=CC(=C3C1=O)[N+]([O-])=O
Molecular Weight 468.72
Reaxy-Rn 22334922
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=22334922&ln=

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:

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

9 results found

Lot NumberCertificate TypeDateItem
L2315104Certificate of AnalysisDec 01, 2023 J414220
L2315105Certificate of AnalysisDec 01, 2023 J414220
L2315106Certificate of AnalysisDec 01, 2023 J414220
L2315107Certificate of AnalysisDec 01, 2023 J414220
L2315108Certificate of AnalysisDec 01, 2023 J414220
L2315109Certificate of AnalysisDec 01, 2023 J414220
L2315110Certificate of AnalysisDec 01, 2023 J414220
L2315111Certificate of AnalysisDec 01, 2023 J414220
L2315112Certificate of AnalysisDec 01, 2023 J414220
Chemical and Physical Properties
SolubilitySolubility (25°C) In vitro DMSO: 12 mg/mL (25.6 mM); Water: Insoluble; Ethanol: Insoluble;
DMSO(mg / mL) Max Solubility12
DMSO(mM) Max Solubility25.6016385048643
Water(mg / mL) Max Solubility<1
Solution Calculators
Reviews

Customer Reviews

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