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CAIX Inhibitor S4 1330061-67-0

CAIX Inhibitor S4 1330061-67-0

CAS No.: 1330061-67-0

CAIX Inhibitor S4 is an inhibitor (blocker/antagonist) of carbonic anhydrase IX. It is more selective for CAIX than CAI
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This product is for research use only, not for human use. We do not sell to patients.

CAIX Inhibitor S4 is an inhibitor (blocker/antagonist) of carbonic anhydrase IX. It is more selective for CAIX than CAI and CAII, but inhibits CAXII. In the MDA-MB-231 mouse xenograft model, it reduced the number of lung metastases but not the growth of primary tumors.

Physicochemical Properties


Molecular Formula C15H17N3O4S
Molecular Weight 335.378
Exact Mass 335.093
Elemental Analysis C, 53.72; H, 5.11; N, 12.53; O, 19.08; S, 9.56
CAS # 1330061-67-0
PubChem CID 53342705
Appearance White to off-white solid powder
Density 1.4±0.1 g/cm3
Index of Refraction 1.663
LogP 2.51
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 4
Heavy Atom Count 23
Complexity 487
Defined Atom Stereocenter Count 0
SMILES

S(N)(=O)(=O)OC1C=CC(=CC=1)NC(NC1C=C(C)C=C(C)C=1)=O

InChi Key HGVHSNXRZYOTPD-UHFFFAOYSA-N
InChi Code

InChI=1S/C15H17N3O4S/c1-10-7-11(2)9-13(8-10)18-15(19)17-12-3-5-14(6-4-12)22-23(16,20)21/h3-9H,1-2H3,(H2,16,20,21)(H2,17,18,19)
Chemical Name

4-(3-(3,5-dimethylphenyl)ureido)phenyl sulfamate
Synonyms

CAIX Inhibitor S4
HS Tariff Code 2934.99.9001
Storage

Powder-20°C 3 years

4°C 2 years

In solvent -80°C 6 months

-20°C 1 month

Shipping Condition Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)

Biological Activity


ln Vitro In a dose-dependent way, CAIX Inhibitor S4 (1-100 μM; 24 h) reduces the growth of MDA-MB-231, HCT116, and HT29 cells [1]. Under hypoxic conditions, eGFP-MDA-MB-231 cell migration is inhibited in a concentration-dependent manner by CAIX Inhibitor S4 (3.3-33 μM; 24 h) [1]. Under hypoxic conditions, CAIX Inhibitor S4 (33 μM; 15-60 min) decreases the spreading of MDA-MB-231 cells; however, under normoxic conditions, there is minimal delay [1].
ln Vivo CAIX Inhibitor S4 (10 mg/kg; i.p. for 14 days) inhibits metastatic tumor burden in the MDA-MB-231 model without affecting primary tumor growth or mouse condition [1].
Cell Assay Cell proliferation assay[1]
Cell Types: MDA-MB-231, HCT116 and HT29 Cell
Tested Concentrations: 1, 10, 100 μM
Incubation Duration: 24 hrs (hours)
Experimental Results: Inhibition of cell proliferation of MDA-MB-231, HCT116 and HT29 cells, IC50 481 μM, >1000 μM and 20 μM respectively.
Animal Protocol Animal/Disease Models: Female nu/nu CBA mice (10-12 weeks) are injected with eGFP-MDA-MB-231 cells [1]
Doses: 10 mg/kg
Route of Administration: intraperitoneal (ip) injection every day, "5 days, 2 days off" Results of the 14-day dosing regimen: Dramatically diminished metastatic tumor burden in the lungs of mice bearing orthotopic eGFP-MDA-MB-231 tumors. Average body weights were similar between vehicle and S4-treated mice throughout the experiments.
References

[1]. Antimetastatic effect of sulfamate carbonic anhydrase IX inhibitors in breast carcinoma xenografts. J Med Chem. 2012 Jun 14;55(11):5591-600.


Solubility Data


Solubility (In Vitro) DMSO : ~250 mg/mL (~745.42 mM)
Solubility (In Vivo) Note: Listed below are some common formulations that may be used to formulate products with low water solubility (e.g. < 1 mg/mL), you may test these formulations using a minute amount of products to avoid loss of samples.

Injection Formulations
(e.g. IP/IV/IM/SC)
Injection Formulation 1: DMSO : Tween 80: Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution 50 μL Tween 80 850 μL Saline)
*Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH ₂ O to obtain a clear solution.
Injection Formulation 2: DMSO : PEG300 :Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL DMSO 400 μLPEG300 50 μL Tween 80 450 μL Saline)
Injection Formulation 3: DMSO : Corn oil = 10 : 90 (i.e. 100 μL DMSO 900 μL Corn oil)
Example: Take the Injection Formulation 3 (DMSO : Corn oil = 10 : 90) as an example, if 1 mL of 2.5 mg/mL working solution is to be prepared, you can take 100 μL 25 mg/mL DMSO stock solution and add to 900 μL corn oil, mix well to obtain a clear or suspension solution (2.5 mg/mL, ready for use in animals).
Injection Formulation 4: DMSO : 20% SBE-β-CD in saline = 10 : 90 [i.e. 100 μL DMSO 900 μL (20% SBE-β-CD in saline)]
*Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution.
Injection Formulation 5: 2-Hydroxypropyl-β-cyclodextrin : Saline = 50 : 50 (i.e. 500 μL 2-Hydroxypropyl-β-cyclodextrin 500 μL Saline)
Injection Formulation 6: DMSO : PEG300 : castor oil : Saline = 5 : 10 : 20 : 65 (i.e. 50 μL DMSO 100 μLPEG300 200 μL castor oil 650 μL Saline)
Injection Formulation 7: Ethanol : Cremophor : Saline = 10: 10 : 80 (i.e. 100 μL Ethanol 100 μL Cremophor 800 μL Saline)
Injection Formulation 8: Dissolve in Cremophor/Ethanol (50 : 50), then diluted by Saline
Injection Formulation 9: EtOH : Corn oil = 10 : 90 (i.e. 100 μL EtOH 900 μL Corn oil)
Injection Formulation 10: EtOH : PEG300:Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL EtOH 400 μLPEG300 50 μL Tween 80 450 μL Saline)

Oral Formulations Oral Formulation 1: Suspend in 0.5% CMC Na (carboxymethylcellulose sodium)
Oral Formulation 2: Suspend in 0.5% Carboxymethyl cellulose
Example: Take the Oral Formulation 1 (Suspend in 0.5% CMC Na) as an example, if 100 mL of 2.5 mg/mL working solution is to be prepared, you can first prepare 0.5% CMC Na solution by measuring 0.5 g CMC Na and dissolve it in 100 mL ddH2O to obtain a clear solution; then add 250 mg of the product to 100 mL 0.5% CMC Na solution, to make the suspension solution (2.5 mg/mL, ready for use in animals).
Oral Formulation 3: Dissolved in PEG400
Oral Formulation 4: Suspend in 0.2% Carboxymethyl cellulose
Oral Formulation 5: Dissolve in 0.25% Tween 80 and 0.5% Carboxymethyl cellulose
Oral Formulation 6: Mixing with food powders

Note: Please be aware that the above formulations are for reference only. InvivoChem strongly recommends customers to read literature methods/protocols carefully before determining which formulation you should use for in vivo studies, as different compounds have different solubility properties and have to be formulated differently.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 2.9817 mL 14.9085 mL 29.8169 mL
5 mM 0.5963 mL 2.9817 mL 5.9634 mL
10 mM 0.2982 mL 1.4908 mL 2.9817 mL
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.