research use only
Cat.No.S5645
| Related Targets | Bcl-2 Caspase PD-1/PD-L1 Ferroptosis p53 Apoptosis related Synthetic Lethality STAT TNF-alpha Ras |
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| Other Heme Oxygenase Inhibitors | Fraxetin Ferulaldehyde Tin protoporphyrin IX dichloride Momordica grosvenori Extract |
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In vitro |
DMSO
: 20 mg/mL
(30.67 mM)
Water : Insoluble |
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In vivo |
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| Molecular Weight | 651.94 | Formula | C34H32ClFeN4O4 |
Storage (From the date of receipt) | 3 years -20°C(in the dark) powder |
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| CAS No. | 16009-13-5 | -- | Storage of Stock Solutions |
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| Synonyms | protohemin | Smiles | CC1=C(C2=CC3=C(C(=C([N-]3)C=C4C(=C(C(=N4)C=C5C(=C(C(=N5)C=C1[N-]2)C)C=C)C)C=C)C)CCC(=O)O)CCC(=O)O.[Cl-].[Fe+3] | ||
| In vitro |
Treatment of hemin or AFC damped the expression of TFRC in CT26 cells, which can be significantly rescued by overexpression of OTUD1. |
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| In vivo |
Following the i.p. administration of Hemin (100 μM/kg), the HO-1 level in the renal cortex begins to increase gradually. The HO-1 level reaches its peak 24 h after this compound preconditioning. HO-1 is expressed mainly in the renal tubules. The HO-2 level in the kidney does not change following this chemical preconditioning. |
References |
(data from https://clinicaltrials.gov, updated on 2024-05-22)
| NCT Number | Recruitment | Conditions | Sponsor/Collaborators | Start Date | Phases |
|---|---|---|---|---|---|
| NCT03338816 | Completed | Acute Hepatic Porphyria|Acute Intermittent Porphyria|Porphyria Acute Intermittent|Acute Porphyria|Hereditary Coproporphyria (HCP)|Variegate Porphyria (VP)|ALA Dehydratase Deficient Porphyria (ADP) |
Alnylam Pharmaceuticals |
November 16 2017 | Phase 3 |
| NCT02949830 | Completed | Acute Intermittent Porphyria |
Alnylam Pharmaceuticals |
October 2016 | Phase 1|Phase 2 |
| NCT01855841 | Completed | Post-ERCP Acute Pancreatitis |
Erasme University Hospital |
April 2012 | Phase 2 |
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