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H-SER-OH application areas
- Medicine and Biochemistry
Used as peptide synthesis intermediates for the preparation of drugs (such as antibiotics and anticancer peptides). Its derivative, H-Ser-Asp-OH, exhibits biological activity and may participate in signal transduction.
- Chiral Synthesis
In asymmetric catalysis, serine derivatives can serve as chiral ligands to control reaction stereoselectivity.
- Research Tools
Used in cell culture, protein structure studies, and metabolic pathway analysis.
Product information
| L-Serine Foods test item | Index |
| H-SER-OH CAS NO. | 56-45-1 |
| Water Solubility | 250g/L (20 º C) |
| Maximum Wavelength (λ max) | λ: 260nm Amax: 0.05 λ: 280nm Amax: 0.05 |
| Sublimation Point | 150 º C |
| LogP | -1.580 |
| Stability | Stable. Incompatible with strong oxidizing agents. |
Hereditary sensory and autonomic neuropathy type 1 (HSAN1) is clinically characterized
by early-onset dissociated sensory impairment, affecting pain and temperature sensation,
while vibration and joint position senses are preserved. This is due to length-dependent
axonal neuropathy.
Many patients frequently experience severe positive sensory symptoms such as radiating
or burning pain in the limbs, and some may undergo a brief period of hyperalgesia in the
early stages. Due to severe sensory impairment, many patients develop neuropathic ulcers
and Charcot joints, and may even require amputations.
Most patients exhibit significant motor dysfunction early in the disease course. Autopsy
reports of HSAN1 patients reveal marked degeneration of dorsal root ganglion cells and
a reduction in myelinated axons in peripheral nerves . Unmyelinated axons are also affected,
though reportedly to a lesser extent.
H-SER-OH Transgenic mice carrying the C133W mutation closely mimic the disease
progression observed in humans. By 10 months of age, these mice develop hyperalgesia,
motor dysfunction, thinning of peripheral nerve myelin, loss of visceral innervation, and
signs of neuronal stress in the dorsal root ganglia.

By 12 months, the hyperalgesia subsides, and by 14 months, they exhibit small-fiber
sensory neuropathy and sensory-motor deficits similar to those seen in HSAN1 patients.
Unlike humans, C133W transgenic mice exhibit infertility, with reduced sperm count, sperm
motility, and testicular weight, features that can be reversed by forced overexpression of
the wild-type gene in double-transgenic mice.


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