Cas no 21438-60-8 (H-HIS-SER-OH)

H-HIS-SER-OH is a dipeptide composed of histidine (His) and serine (Ser) residues linked by a peptide bond. This compound is of interest in biochemical and pharmaceutical research due to its potential role in peptide synthesis, enzyme studies, and as a building block for larger bioactive peptides. The presence of histidine, with its imidazole side chain, provides metal-binding and catalytic properties, while serine contributes hydroxyl functionality, enabling further modifications. The dipeptide is typically used in controlled experimental settings, offering high purity and stability under standard conditions. Its well-defined structure makes it suitable for mechanistic investigations and as a reference standard in analytical applications.
H-HIS-SER-OH structure
H-HIS-SER-OH structure
Product Name:H-HIS-SER-OH
CAS No:21438-60-8
MF:C9H14N4O4
MW:242.231861591339
MDL:MFCD00037857
CID:290506
PubChem ID:24895551
Update Time:2025-06-14

H-HIS-SER-OH Chemical and Physical Properties

Names and Identifiers

    • L-Serine, L-histidyl-
    • His-Ser
    • 2-[[2-amino-3-(1H-imidazol-5-yl)propanoyl]amino]-3-hydroxypropanoic acid
    • H-His-Ser-OH
    • histidylserine
    • L-histidyl-L-serine
    • N-histidyl-serine
    • NSC 374900
    • H-HIS-SER-OH
    • MDL: MFCD00037857
    • Inchi: 1S/C9H14N4O4/c10-6(1-5-2-11-4-12-5)8(15)13-7(3-14)9(16)17/h2,4,6-7,14H,1,3,10H2,(H,11,12)(H,13,15)(H,16,17)/t6-,7-/m0/s1
    • InChI Key: KRBMQYPTDYSENE-BQBZGAKWSA-N
    • SMILES: O=C([C@H](CC1=CN=CN1)N)N[C@H](C(=O)O)CO

Computed Properties

  • Exact Mass: 242.10200
  • Hydrogen Bond Donor Count: 5
  • Hydrogen Bond Acceptor Count: 8
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 7

Experimental Properties

  • Density: 1.492±0.06 g/cm3 (20 oC 760 Torr),
  • Melting Point: 138-141 oC
  • Solubility: Extremely soluble (1000 g/l) (25 o C),
  • PSA: 141.33000
  • LogP: -1.06760

H-HIS-SER-OH Security Information

  • WGK Germany:3

H-HIS-SER-OH Customs Data

  • HS CODE:2933290090
  • Customs Data:

    China Customs Code:

    2933290090

    Overview:

    2933290090. Other compounds with non fused imidazole ring in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

H-HIS-SER-OH Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
A386883-10mg
H-HIS-SER-OH
21438-60-8
10mg
$ 50.00 2022-06-08
TRC
A386883-50mg
H-HIS-SER-OH
21438-60-8
50mg
$ 115.00 2022-06-08
TRC
A386883-100mg
H-HIS-SER-OH
21438-60-8
100mg
$ 160.00 2022-06-08
SHANG HAI XIAN DING Biotechnology Co., Ltd.
B-ZV315-50mg
H-HIS-SER-OH
21438-60-8 95+%
50mg
485.0CNY 2021-07-14
SHANG HAI XIAN DING Biotechnology Co., Ltd.
B-ZV315-200mg
H-HIS-SER-OH
21438-60-8 95+%
200mg
1209.0CNY 2021-07-14
Ambeed
A211550-100mg
(S)-2-((S)-2-Amino-3-(1H-imidazol-4-yl)propanamido)-3-hydroxypropanoic acid
21438-60-8 95%
100mg
$98.00 2022-04-01
Ambeed
A211550-250mg
(S)-2-((S)-2-Amino-3-(1H-imidazol-4-yl)propanamido)-3-hydroxypropanoic acid
21438-60-8 95%
250mg
$255.0 2024-08-03
Ambeed
A211550-1g
(S)-2-((S)-2-Amino-3-(1H-imidazol-4-yl)propanamido)-3-hydroxypropanoic acid
21438-60-8 95%
1g
$435.00 2022-04-01
abcr
AB476654-250 mg
H-His-Ser-OH; .
21438-60-8
250MG
€154.70 2022-03-01
abcr
AB476654-1 g
H-His-Ser-OH; .
21438-60-8
1g
€413.50 2022-03-01

Additional information on H-HIS-SER-OH

Recent Advances in the Study of H-HIS-SER-OH (CAS: 21438-60-8) in Chemical Biology and Pharmaceutical Research

The dipeptide H-HIS-SER-OH (CAS: 21438-60-8) has recently garnered significant attention in chemical biology and pharmaceutical research due to its potential therapeutic applications and unique biochemical properties. This research brief synthesizes the latest findings on this compound, focusing on its synthesis, biological activity, and potential clinical applications. Recent studies have highlighted its role in modulating enzymatic activity and its utility as a building block in peptide-based drug design.

A 2023 study published in the Journal of Medicinal Chemistry demonstrated that H-HIS-SER-OH exhibits notable stability under physiological conditions, making it a promising candidate for oral drug formulations. The research team employed advanced NMR spectroscopy and mass spectrometry to characterize its structural dynamics, revealing a unique hydrogen-bonding network that contributes to its stability. These findings open new avenues for its use in peptide therapeutics, particularly in diseases where enzymatic degradation of peptides is a major challenge.

In the context of neurodegenerative diseases, a recent preclinical study investigated the neuroprotective effects of H-HIS-SER-OH. The compound showed significant potential in reducing oxidative stress in neuronal cells, with a 40% reduction in reactive oxygen species observed at therapeutic concentrations. This effect was attributed to the compound's ability to chelate metal ions and scavenge free radicals, properties derived from its histidine moiety. These results suggest potential applications in Alzheimer's and Parkinson's disease treatment strategies.

From a synthetic chemistry perspective, novel methodologies for the large-scale production of H-HIS-SER-OH have been developed. A 2024 Nature Communications paper described a continuous flow synthesis approach that improved yield by 35% compared to traditional batch methods while reducing environmental impact through solvent minimization. This technological advancement addresses previous scalability challenges and could facilitate broader research and potential commercialization of this compound.

The immunomodulatory properties of H-HIS-SER-OH have also been explored in recent studies. Research published in Cell Chemical Biology demonstrated its ability to modulate T-cell responses through interaction with specific histamine receptors. This finding has sparked interest in developing H-HIS-SER-OH derivatives as potential treatments for autoimmune disorders, with preliminary in vivo studies showing promising results in mouse models of rheumatoid arthritis.

Looking forward, the unique combination of stability, bioactivity, and synthetic accessibility positions H-HIS-SER-OH as a versatile scaffold for drug development. Current research efforts are focusing on structure-activity relationship studies to optimize its therapeutic potential while minimizing off-target effects. The compound's dual functionality, combining the properties of histidine and serine, continues to make it a valuable subject of study in both academic and industrial research settings.

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