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SLC-0111

SKU: orb1225910

Description

SLC-0111 is a sulfonamide carbonic anhydrase (CA, EC 4.2.1.1) inhibitor with IC50 of 45 nM and 4.5 nM for tumor-associated enzymes hCA IX and hCA XII; showed selective CA IX/XII inhibitory profiles, displays >20-fold and >100-fold selectivity over hCA II and hCA I, respectively; reduces tumor cell growth and increases apoptotic cell death in prostate cancer cells.Pancreatic Cancer Phase 1(In Vitro):U-104 (SLC-0111) is a potent exosome inhibitor.U-104 has low inhibition for CA I (Ki=5080 nM) and CA II (Ki=9640 nM).U-104 (50 μM; for 72 hours) blocks the mesenchymal phenotype in the cancer stem cells population in hypoxia condition of 4T1 cells. U-104 (<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.\n(In Vivo):U-104 (19, 38 mg/kg; daily; for 27 days) inhibits primary tumor growth in the mice implanted orthotopically with MDA-MB-231 LM2-4Luc+ cells. U-104 (19 mg/kg; daily; for 5 days) inhibits metastases formation in the 4T1 experimental metastasis mice model.U-104 (38 mg/kg; i.p.; from 11 to 27 days) significantly delays primary tumor growth and reduces cancer stem cell population in NOD/SCID mice orthotopically implanted with MDA-MB-231 LM2-4Luc+ cells.U-104 (50 mg/kg; oral gavage; continuously for 4 days and suspended for 1 day; from 10 to 30 days) shows a significant delay in tumor growth in Balb/c mice orthotopically implanted with 4T1 cells.

Images & Validation

Key Properties

CAS Number178606-66-1
MW309.315
Purity>98% (HPLC)
FormulaC13H12FN3O3S
SMILESFC1=CC=C(C=C1)NC(NC2=CC=C(C=C2)S(N)(=O)=O)=O
TargetCarbonic Anhydrase
SolubilityDMSO: 30.9 mg/mL (100 mM) ( < 1 mg/ml refers to the product slightly soluble or insoluble )

Bioactivity

In Vivo
U-104 (19, 38 mg/kg; daily; for 27 days) inhibits primary tumor growth in the mice implanted orthotopically with MDA-MB-231 LM2-4Luc+ cells. U-104 (19 mg/kg; daily; for 5 days) inhibits metastases formation in the 4T1 experimental metastasis mice model. U-104 (38 mg/kg; i.p.; from 11 to 27 days) significantly delays primary tumor growth and reduces cancer stem cell population in NOD/SCID mice orthotopically implanted with MDA-MB-231 LM2-4Luc+ cells. U-104 (50 mg/kg; oral gavage; continuously for 4 days and suspended for 1 day; from 10 to 30 days) shows a significant delay in tumor growth in Balb/c mice orthotopically implanted with 4T1 cells.
In Vitro
U-104 (SLC-0111) is a potent exosome inhibitor. U-104 has low inhibition for CA I (Ki= 5080 nM) and CA II (Ki= 9640 nM). U-104 (50 μM; for 72 hours) blocks the mesenchymal phenotype in the cancer stem cells population in hypoxia condition of 4T1 cells. U-104 (< 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.

Storage & Handling

StorageStorage temperature: -20°C. Stability: ≥ 2 years
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

SLC 0111 | SLC0111

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SLC-0111 (orb1225910)

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Available Sizes

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5 mg
$ 70.00
10 mg
$ 90.00
25 mg
$ 160.00
50 mg
$ 240.00
100 mg
$ 420.00
200 mg
$ 660.00
500 mg
$ 1,070.00