Structure of UAMC-3203 HCl
CAS No.: 2271358-65-5
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
UAMC-3203 HCl is a potent and selective Ferroptosis inhibitor with an IC50 of 12 nM.
Synonyms: UAMC-3203 (hydrochloride); UAMC-3203 hydrochloride
4.5
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Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
CAS No. : | 2271358-65-5 |
Formula : | C25H38ClN5O2S |
M.W : | 508.12 |
SMILES Code : | O=S(C1=CC=C(NC2CCCCC2)C(NCC3=CC=CC=C3)=C1)(NCCN4CCNCC4)=O.[H]Cl |
Synonyms : |
UAMC-3203 (hydrochloride); UAMC-3203 hydrochloride
|
MDL No. : | MFCD32062758 |
InChI Key : | WBZHHIZXEXJBSM-UHFFFAOYSA-N |
Pubchem ID : | 137701964 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
A549 | 25 nM | 24 hours | Inhibit FZKA-induced lipid peroxidation | Front Pharmacol. 2022 Apr 13;13:851680 |
H1299 | 25 nM | 24 hours | Inhibit FZKA-induced lipid peroxidation | Front Pharmacol. 2022 Apr 13;13:851680 |
H1650 | 25 nM | 24 hours | Inhibit FZKA-induced lipid peroxidation | Front Pharmacol. 2022 Apr 13;13:851680 |
PC9 | 25 nM | 24 hours | Inhibit FZKA-induced lipid peroxidation | Front Pharmacol. 2022 Apr 13;13:851680 |
Human corneal epithelial (HCE) cells | 10 nM, 1 µM, 10 µM, 50 µM | 3 hours | Assess cytotoxicity of UAMC-3203. Cell viability was reduced to 75% and 39.2% at 10 µM and 50 µM, respectively, whereas 10 nM and 1 µM caused no toxicity. | Pharmaceutics. 2022 Dec 29;15(1):118 |
Bone marrow-derived macrophages (BMDMs) | 1 µM | 4 hours | To evaluate the protective effect of UAMC-3203 on erythrophagocytosis-induced ferroptosis. Results showed that UAMC-3203 significantly reduced lipid peroxidation and cell death. | Angiogenesis. 2023 Nov;26(4):505-522 |
Human corneal epithelial (HCE) cells | 10 nM, 1 µM, 10 µM, 50 µM | 72 hours | Evaluate the effect of UAMC-3203 on cell migration. Results showed significantly higher HCE cell migration at 10 nM and 1 µM (p<0.001 and p=0.003 vs. negative control), while 10 µM and 50 µM showed no notable effects. | Pharmaceutics. 2022 Dec 29;15(1):118 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
Mice | Choline-deficient L-amino acid-defined high-fat diet (CDAHFD) and high-fat high-fructose diet (HFHFD) models | Subcutaneous osmotic minipumps | 12.35 mg/kg | 4 weeks | To evaluate the inhibitory effect of UAMC-3203 on ferroptosis in CDAHFD and HFHFD models. Results showed that UAMC-3203 reduced ALT and steatosis, but had little effect on hepatocyte ballooning, lobular inflammation, and fibrosis. | Cell Death Differ. 2024 Sep;31(9):1113-1126 |
ApoE−/− Fbn1C1039G+/− mice | Western-type diet (WD)-induced atherosclerosis model | Subcutaneous osmotic minipumps | 12.35 mg/kg/day | Daily administration for 8 weeks | To evaluate the effect of UAMC-3203 on atherosclerosis. Results showed that UAMC-3203 significantly reduced carotid plaque thickness, especially in plaques with confirmed IP angiogenesis or hemorrhage. | Angiogenesis. 2023 Nov;26(4):505-522 |
Female C57BL/6 mice | Mild spinal cord injury model | Intraperitoneal injection | 15 mg/kg | Daily for either early treatment group (1-14 days) or delayed treatment group (28-42 days) | To evaluate the effects of UAMC-3203 on locomotor recovery and secondary damage after mild spinal cord injury. Results showed that both early and delayed treatments improved locomotor recovery and reduced secondary damage. | Acta Neuropathol. 2024 Jun 22;147(1):106 |
Wistar rats | Spinal cord injury model | Intraperitoneal injection | 5 mg/kg | 7 consecutive days | UAMC-3203 inhibits ferroptosis, reduces spinal cord tissue damage and motor neuron loss, mitigates the inflammatory response post-spinal cord injury, and enhances the restoration of motor function in rats | Sci Rep. 2024 Aug 30;14(1):20180 |
Tags: UAMC-3203 | UAMC3203 | UAMC 3203 | Ferroptosis | inhibitor | 2271358-65-5 |
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