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Chemical structure of Hepcidin-20 (human)

GA22328

Hepcidin-20 (human)

Also known as (2S,3R)-2-[[(2S)-6-amino-2-[[(1R,4R,7S,10S,13S,16S,19R,25S,28R,31R,36R,39S,42S,45R,55R)-16-(4-aminobutyl)-45-[[(2S,3S)-2-amino-3-methylpentanoyl]amino]-39-benzyl-42-[(2S)-butan-2-yl]-10-(3-carbamimidamidopropyl)-13-(hydroxymethyl)-7-(1H-imidazol-5-ylmethyl)-25-(2-methylsulfanylethyl)-2,5,8,11,14,17,20,23,26,29,38,41,44,51,54,61-hexadecaoxo-33,34,47,48,57,58,63,64-octathia-3,6,9,12,15,18,21,24,27,30,37,40,43,50,53,60-hexadecazatetracyclo[26.21.10.44,19.236,55]pentahexacontane-31-carbonyl]amino]hexanoyl]amino]-3-hydroxybutanoic acid

Hepcidin-20, a degradation product of hepcidin-25 found in plasma and urine, shows an increased antimicrobial activity compared to the full-length peptide, but it is not involved in iron metabolism

ChemicalCAS342790-23-2MW2191.77FormulaC85H135N27O23S9
CAS number
342790-23-2
Molecular weight
2191.77
Formula
C85H135N27O23S9
Solubility
Soluble in DMSO
InChIKey
KCGSCDOCNSLUQM-BJMJBLFRSA-N
Catalogue number
GA22328
Brand
GLPBIO
Computed properties PubChem CID 131852664 · XLogP -7.5 · TPSA 1030 Ų · H-bond donors 29
XLogP
-7.5
TPSA
1030 Ų
H-bond donors
29
H-bond acceptors
37
Rotatable bonds
33
Heavy atoms
144

SMILES CC[C@H](C)[C@H]1C(=O)N[C@H](C(=O)N[C@H]2CSSC[C@H](NC(=O)[C@@H]3CSSC[C@@H](C(=O)NCC(=O)N[C@@H](CSSC[C@@H](C(=O)N1)NC(=O)[C@H]([C@@H](C)CC)N)C(=O)N[C@H]4CSSC[C@@H](C(=O)NCC(=O)N[C@H](C(=O)N3)CCSC)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC4=O)CC5=CN=CN5)CCCNC(=N)N)CO)CCCCN)NC2=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(=O)O)CC6=CC=CC=C6

Computed descriptors from PubChem (CID 131852664), public domain. Identity cross-checked against the supplier's molecular formula and weight — verify before use.

Ordering in Israel

Lead time
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Pricing
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Documents
Lot certificate of analysis and manufacturer SDS are emailed with your order confirmation.
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