U-104

Catalog No.S2866 Batch:S286604

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Technical Data

Formula

C13H12FN3O3S

Molecular Weight 309.32 CAS No. 178606-66-1
Solubility (25°C)* In vitro DMSO 62 mg/mL (200.43 mM)
Water Insoluble
Ethanol Insoluble
In vivo (Add solvents to the product individually and in order)
Homogeneous suspension
CMC-NA
≥5mg/ml Taking the 1 mL working solution as an example, add 5 mg of this product to 1 ml of CMC-Na solution, mix evenly to obtain a homogeneous suspension with a final concentration of 5 mg/ml.
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
* Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

Biological Activity

Description U-104 (MST-104, NSC 213841, SLC-0111, WBI-5111) is a potent carbonic anhydrase (CA) inhibitor for CA IX and CA XII with Ki of 45.1 nM and 4.5 nM, respectively, very low inhibition for CA I and CA II.
Targets
CAXII [1]
(Cell-free assay)
CAIX [1]
(Cell-free assay)
4.5 nM(Ki) 45.1 nM(Ki)
In vitro U-104 (50  μM) blocks the mesenchymal phenotype in the cancer stem cells population in hypoxia condition of 4T1 cells. This compound (<50  μM) significantly reduces migration in a dose-dependent manner in metastatic MDA-MB-231 LM2-4Luc+ cells , with cells growing as compact colonies similar to parental MDA-MB-231 cells. [2] This chemical possesses aromatic groups at the second nitrogen ureido group. [3]
In vivo U-104 (38 mg/kg) inhibits primary tumor growth in the mice implanted orthotopically with MDA-MB-231 LM2-4Luc+ cells. This compound (19 mg/kg) inhibits metastases formation in the 4T1 experimental metastasis mice model. [1] This chemical (38 mg/kg) significantly delay primary tumor growth and reduces cancer stem cell population in NOD/SCID mice orthotopically implanted with MDA-MB-231 LM2-4Luc+ cells. It (5 mg/mL, oral gavage) shows a significant delay in tumor growth in Balb/c mice orthotopically implanted with 4T1 cells. [2]

Protocol (from reference)

Animal Study:[2]
  • Animal Models

    Balb/c mice orthotopically implanted with 4T1 cells.

  • Dosages

    5 mg/mL

  • Administration

    Oral gavage

References

  • https://pubmed.ncbi.nlm.nih.gov/21415165/
  • https://pubmed.ncbi.nlm.nih.gov/23208505/
  • https://pubmed.ncbi.nlm.nih.gov/21361354/

Customer Product Validation

<p>(c-f) Effects of the CAIX inhibitor U-104 (75 μM) on cell proliferation by Pt45.P1/asTF+ cells (c, e) or Pt45.P1 cells (d, f) under advanced-stage (c, d) or early-stage conditions (e, f). At the indicated times, WST-1 uptake was measured by colorimetry. The error bars are s.e.m. * Indicates significance at P<0.05.</p>

, , Lab Invest, 2016, 96(12):1234-1245

Regression coefficients from the second-order stepwise linear regression model are provided based on the data obtained from Search 2.1 (B) The results allow the least effective compounds to be eliminated. Red is used to highlighted drug contributions that do not help to inhibit cell viability, orange bars are used to indicate minimal contributions and green highlights synergistic drug interactions. The inset in B shows the linear fit of modelled data with theoretical quartiles versus standardized residuals and the corresponding R2-values for each model. Significance is indicated by asterisks, **p < 0.01 and *p < 0.05.

Data from [ , , Sci Rep, 2015, 5:14508 ]

Synchronous with the decrease in CA9 expression, the TMZ + U‑104 combination substantially decreased the expression of SOX9, p-AKT and BCL‑2 in glioma cells, and increased the expression of BAX, compared to the TMZ alone group.

Data from [ , , Int J Oncol, 2018, 53(1):189-202 ]

Selleck's U-104 Has Been Cited by 11 Publications

Alterations in gene expression associated with invasion of RAS-mutant thyroid tumors and their potential diagnostic and therapeutic utility [ Eur Thyroid J, 2025, 14(3)e250022] PubMed: 40440326
Depletion of slow-cycling PDGFRα+ADAM12+ mesenchymal cells promotes antitumor immunity by restricting macrophage efferocytosis [ Nat Immunol, 2023, 24(11):1867-1878] PubMed: 37798557
SLC-0111, an inhibitor of carbonic anhydrase IX, attenuates hepatoblastoma cell viability and migration [ Front Oncol, 2023, 13:1118268] PubMed: 36776327
CA9 and PRELID2; hypoxia-responsive potential therapeutic targets for pancreatic ductal adenocarcinoma as per bioinformatics analyses [ J Pharmacol Sci, 2023, 10.1016/j.jphs.2023.10.003] PubMed: 37973221
A nanoplatform to boost multi-phases of cancer-immunity-cycle for enhancing immunotherapy [ J Control Release, 2021, 339:403-415] PubMed: 34655676
Hotspots of Aberrant Enhancer Activity in Fibrolamellar Carcinoma Reveal Candidate Oncogenic Pathways and Therapeutic Vulnerabilities. [ Cell Rep, 2020, 14;31(2):107509] PubMed: 32294439
Integrating Phenotypic Search and Phosphoproteomic Profiling of Active Kinases for Optimization of Drug Mixtures for RCC Treatment [ Cancers (Basel), 2020, 12(9)E2697] PubMed: 32967224
One-pot synthesis of pH-responsive charge-switchable PEGylated nanoscale coordination polymers for improved cancer therapy [Yang Y, et al. Biomaterials, 2018, 156:121-133] PubMed: 29195181
Association between SOX9 and CA9 in glioma, and its effects on chemosensitivity to TMZ [Xu X, et al. Int J Oncol, 2018, 53(1):189-202] PubMed: 29749469
Activation of carbonic anhydrase IX by alternatively spliced tissue factor under late-stage tumor conditions [Ramchandani D, et al. Lab Invest, 2016, 10.1038/labinvest.2016.103] PubMed: 27721473

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SHIPPING AND STORAGE
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