S4503

DL-Serine hydroxamate

≥97% (TLC), suitable for ligand binding assays

Manufacturer: Sigma Aldrich

CAS Number: 55779-32-3

Synonym(S): SHX

Select a Size

Pack Size SKU Availability Price
250 MG S4503-250-MG In Stock ₹ 42,401.53
1 G S4503-1-G In Stock ₹ 1,02,014.80

S4503 - 250 MG

₹ 42,401.53

In Stock

Quantity

1

Base Price: ₹ 42,401.53

GST (18%): ₹ 7,632.275

Total Price: ₹ 50,033.805

Quality Level

200

Assay

≥97% (TLC)

form

powder

technique(s)

ligand binding assay: suitable

color

white to off-white

application(s)

cell analysis

storage temp.

−20°C

SMILES string

NC(CO)C(=O)NO

InChI

1S/C3H8N2O3/c4-2(1-6)3(7)5-8/h2,6,8H,1,4H2,(H,5,7)

InChI key

LELJBJGDDGUFRP-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
S4503
DL-Serine hydroxamate
Sigma Aldrich ₹ 42,401.53 - ₹ 1,02,014.80
CS-0142371
DL-Serine hydroxamate
ChemScene ₹ 8,128.20 - ₹ 21,390.00
AY06532
55779-32-3 | Propanamide, 2-amino-N,3-dihydroxy-, (±)-
A2B Chem ₹ 11,550.60 - ₹ 25,496.88

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Description

  • Application: Serine has been used as an inhibitor of seryl-tRNA synthetase.[1][2] DL-Serine hydroxamate is used to induce metabolic synthesis of guanosine 3′-diphosphate 5′-diphosphate (ppGpp) in E. coli by amino acid starvation.[3] It is also used to synchronize cell cycle in E. coli cultures by inhibition of tRNA charging.[4]
  • Biochem/physiol Actions: Serine is involved in the one-carbon unit metabolism. It is associated with the biosynthesis of cysteine, ceramide, phosphatidylserine, purine and pyrimidine. In bacteria, it participates in tryptophan synthesis. Gluconeogenesis, one of the important biochemical processes, involves serine, particularly in ruminants. Protein phosphorylation is one such event that utilizes serine. Glycine, a metabolic product of serine, serves as an antioxidant and a neurotransmitter. D-serine is known to activate the N-methyl-D-aspartate (NMDA) receptors of the brain.[5] Serine hydroxamate, a structural analogue of serine prevents seryl-tRNA (transfer ribonucleic acid) charging and thereby decreases phospholipid and nucleic acid synthesis in Escherichia coli.[6][7]

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Quality Level:
200

Assay:
≥97% (TLC)

form:
powder

technique(s):
ligand binding assay: suitable

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white to off-white

application(s):
cell analysis

storage temp.:
−20°C

SMILES string:
NC(CO)C(=O)NO

InChI:
1S/C3H8N2O3/c4-2(1-6)3(7)5-8/h2,6,8H,1,4H2,(H,5,7)

InChI key:
LELJBJGDDGUFRP-UHFFFAOYSA-N

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