ACTH 11-24 acetate(4237-93-8 free base)
CAS No. 79190-56-0
ACTH 11-24 acetate(4237-93-8 free base)( —— )
Catalog No. M37912 CAS No. 79190-56-0
ACTH 11-24 acetate(4237-93-8 free base) (Adrenocorticotropic Hormone (11-24) acetate) is a fragment of adrenocorticotrophin, induces cortisol release.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 67 | Get Quote |
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| 5MG | 84 | Get Quote |
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| 10MG | 113 | Get Quote |
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| 25MG | 196 | Get Quote |
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| 50MG | 294 | Get Quote |
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| 100MG | 415 | Get Quote |
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| 200MG | 579 | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameACTH 11-24 acetate(4237-93-8 free base)
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NoteResearch use only, not for human use.
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Brief DescriptionACTH 11-24 acetate(4237-93-8 free base) (Adrenocorticotropic Hormone (11-24) acetate) is a fragment of adrenocorticotrophin, induces cortisol release.
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DescriptionACTH 11-24 acetate(4237-93-8 free base) (Adrenocorticotropic Hormone (11-24) acetate) is a fragment of adrenocorticotrophin, induces cortisol release. ACTH (11-24) has been identified as a competitive antagonist of ACTH (1-39) and ACTH (1-10) in isolated adrenal cells.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayGPCR/G Protein
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TargetMelanocortin Receptor
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RecptorMelanocortin Receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number79190-56-0
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Formula Weight1712.12
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Molecular FormulaC79H138N24O18
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Purity>98% (HPLC)
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Solubility——
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SMILESCC([C@H](NC([C@@H]1CCCN1C([C@@H](N)CCCCN)=O)=O)C(NCC(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N2CCC[C@H]2C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N3CCC[C@H]3C(O)=O)=O)CC4=CC=C(O)C=C4)=O)C(C)C)=O)CCCCN)=O)C(C)C)=O)=O)CCC/N=C(N)\N)=O)CCC/N=C(N)\N)=O)CCCCN)=O)CCCCN)=O)=O)C.CC(O)=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Setmelanotide
Setmelanotide (RM-493, BIM-22493, IRC-022493) is a peptide, non-selective melanocortin receptor agonist with binding Ki of 3.9/10/2.1 for hMC1R/hMC3R/hMC4R, respectively.
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JNJ-10229570
JNJ-10229570 (JNJ10229570) is a novel potent, selective melanocortin receptor MC1R and MC5R antagonist with binding IC50 of 270 nM and 200 nM, respectively.
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HS 014
Potent and selective melanocortin MC4 receptor antagonist (Ki values are 3.16, 108, 54.4 and 694 nM for cloned human MC4, MC1, MC3 and MC5 receptors respectively). Increases food intake in rats and nociception in mice following central administration in vivo. Also inhibits IL-1β-induced Fos expression in the paraventricular hypothalamus.
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