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FH535 - ≥98%, high purity , CAS No.108409-83-2

    Grade & Purity:
  • ≥98%
In stock
Item Number
F127654
Grouped product items
SKU Size
Availability
Price Qty
F127654-10mg
10mg
3
$64.90
F127654-50mg
50mg
3
$200.90
F127654-250mg
250mg
2
$904.90

Wnt/β-cantenin inhibitor and PPARγ and PPARδ antagonist

Basic Description

Synonyms FH535 | FH-535 | HB0288 | HMS3653N07 | BDBM50509999 | FH535, >=98% (HPLC) | SB19433 | HY-15721 | J-002138 | C13H10Cl2N2O4S | EX-A388 | SMSF0005619 | N-(2-Methyl-4-nitrophenyl)-2,5-dichlorobenzenesulfonamide | beta-Catenin/Tcf Inhibitor, FH535 | beta -Cate
Specifications & Purity ≥98%
Biochemical and Physiological Mechanisms Description:IC50 Value: 1.1uM (Cytotoxicity in the CCLP-1 cell line) [1] FH535 is a compound that suppresses both Wnt/beta-catenin and peroxisome proliferator-activated receptor (PPAR) signaling. FH535antagonizes both PPAR gamma and PPAR delta ligand
Storage Temp Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Note Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

FH535 is a Wnt/β-catenin signaling inhibitor and also a dual PPARγ and PPARδ antagonist.
A cell-permeable compound that inhibits Wnt/β-catenin and PPAR

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Sulfanilides
Intermediate Tree Nodes Not available
Direct Parent Sulfanilides
Alternative Parents Benzenesulfonamides  Benzenesulfonyl compounds  Nitrobenzenes  Nitrotoluenes  Dichlorobenzenes  Nitroaromatic compounds  Aryl chlorides  Organosulfonamides  Aminosulfonyl compounds  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Organic oxides  Organonitrogen compounds  Organopnictogen compounds  Hydrocarbon derivatives  Organochlorides  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Benzenesulfonamide - Sulfanilide - Nitrobenzene - Nitrotoluene - Benzenesulfonyl group - 1,4-dichlorobenzene - Nitroaromatic compound - Chlorobenzene - Halobenzene - Toluene - Aryl halide - Aryl chloride - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic nitro compound - C-nitro compound - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organosulfur compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as sulfanilides. These are organic aromatic compounds containing a sulfanilide moiety, with the general structure RS(=O)(=O)NC1=CC=CC=C1.
External Descriptors Not available

Associated Targets(Human)

5637 (630 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
A 172 (535 Activities)
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A204 (242 Activities)
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A2058 (690 Activities)
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A-375 (9258 Activities)
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A-427 (643 Activities)
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A498 (42825 Activities)
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A673 (619 Activities)
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ACHN (49357 Activities)
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AGS (1999 Activities)
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BT-20 (503 Activities)
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BT-474 (2113 Activities)
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BXPC-3 (2997 Activities)
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C8166 (1658 Activities)
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CA46 (271 Activities)
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CAKI-1 (44928 Activities)
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Calu-1 (518 Activities)
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Calu-3 (339 Activities)
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Calu-6 (398 Activities)
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CAPAN-1 (772 Activities)
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CCRF-CEM (65223 Activities)
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COLO 205 (50209 Activities)
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COR-L23 (253 Activities)
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Daoy (570 Activities)
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Daudi (625 Activities)
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DLD-1 (17511 Activities)
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DMS-79 (150 Activities)
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DMS-273 (14108 Activities)
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DU-145 (51482 Activities)
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EVSA-T (142 Activities)
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G-361 (890 Activities)
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G-401 (156 Activities)
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HL-60 (67320 Activities)
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HT-1080 (3966 Activities)
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HT-29 (80576 Activities)
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HuCCT-1 (128 Activities)
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Huh-7 (12904 Activities)
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HuTu80 (255 Activities)
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IM-9 (160 Activities)
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J82 (505 Activities)
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JAR (316 Activities)
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JIYOYE (162 Activities)
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K562 (73714 Activities)
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KM12 (47707 Activities)
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LoVo (4724 Activities)
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M14 (47487 Activities)
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MCF7 (126967 Activities)
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MDA-MB-361 (612 Activities)
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MDA-MB-453 (1139 Activities)
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MDA-MB-468 (9477 Activities)
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Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
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H4 (48 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
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Plasmodiophora brassicae (194 Activities)
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SARS-CoV-2 (38078 Activities)
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Vero C1008 (1716 Activities)
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Mechanisms of Action

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

Names and Identifiers

IUPAC Name 2,5-dichloro-N-(2-methyl-4-nitrophenyl)benzenesulfonamide
INCHI InChI=1S/C13H10Cl2N2O4S/c1-8-6-10(17(18)19)3-5-12(8)16-22(20,21)13-7-9(14)2-4-11(13)15/h2-7,16H,1H3
InChIKey AXNUEXXEQGQWPA-UHFFFAOYSA-N
Smiles CC1=C(C=CC(=C1)[N+](=O)[O-])NS(=O)(=O)C2=C(C=CC(=C2)Cl)Cl
Isomeric SMILES CC1=C(C=CC(=C1)[N+](=O)[O-])NS(=O)(=O)C2=C(C=CC(=C2)Cl)Cl
Molecular Weight 361.2
Reaxy-Rn 28463026
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=28463026&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.

4 results found

Lot Number Certificate Type Date Item
F2418004 Certificate of Analysis Jun 24, 2024 F127654
H1813151 Certificate of Analysis Feb 21, 2024 F127654
H1813150 Certificate of Analysis Feb 21, 2024 F127654
H1602011 Certificate of Analysis Dec 18, 2023 F127654

Chemical and Physical Properties

Solubility 25°C: DMSO
Refractive Index 1.65
Boil Point(°C) ~526.3° C at 760 mmHg
Melt Point(°C) 202.89°C
Molecular Weight 361.200 g/mol
XLogP3 3.900
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 3
Exact Mass 359.974 Da
Monoisotopic Mass 359.974 Da
Topological Polar Surface Area 100.000 Ų
Heavy Atom Count 22
Formal Charge 0
Complexity 505.000
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

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