Date published: 2026-4-26

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DL-2-Amino-2-thiazoline-4-carboxylic acid (CAS 2150-55-2)

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Alternate Names:
2-Amino-4,5-dihydro-4-thiazolecarboxylic Acid; 2-Iminothiazolidine-4-carboxylic Acid; DL-2-Amino-2-thiazolin-4-carboxylic Acid
CAS Number:
2150-55-2
Molecular Weight:
146.17
Molecular Formula:
C4H6N2O2S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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DL-2-Amino-2-thiazoline-4-carboxylic acid finds widespread utility in various scientific experiments and research endeavors. It plays a role in biochemical and physiological investigations, as well as in the exploration of enzymes and proteins. Additionally, it contributes significantly to the study of cell signaling pathways. The primary function of DL-2-Amino-2-thiazoline-4-carboxylic acid lies in its inhibitory properties towards enzymes and proteins. By selectively binding to the active site of these biomolecules, it effectively impedes their normal functionality. Moreover, this compound also interacts with the cell membrane, obstructing the reception of external signals by the cells. Through these inhibitory actions, DL-2-Amino-2-thiazoline-4-carboxylic acid plays a vital role in elucidating molecular mechanisms and physiological processes.


DL-2-Amino-2-thiazoline-4-carboxylic acid (CAS 2150-55-2) References

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  2. Biotechnological production of amino acids and derivatives: current status and prospects.  |  Leuchtenberger, W., et al. 2005. Appl Microbiol Biotechnol. 69: 1-8. PMID: 16195792
  3. Metabolic control analysis of L-cysteine producing strain TS1138 of Pseudomonas sp.  |  Huai, L., et al. 2009. Biochemistry (Mosc). 74: 288-92. PMID: 19364323
  4. Graphene-like nets of hydrogen-bonded water molecules in the dihydrate of 2-[(2-ammonioethyl)amino]acetate and the structure of its anhydrous hydroiodide salt.  |  Wiklund, T., et al. 2010. Acta Crystallogr C. 66: o410-3. PMID: 20679718
  5. Isolation and genetic improvement of Pseudomonas sp. strain HUT-78, capable of enzymatic production of L-cysteine from DL-2-amino-Δ2-thiazoline-4-carboxylic acid.  |  Yang, B., et al. 2011. J Gen Appl Microbiol. 57: 379-86. PMID: 22353743
  6. Enhanced biocatalytic production of L-cysteine by Pseudomonas sp. B-3 with in situ product removal using ion-exchange resin.  |  Wang, P., et al. 2015. Bioprocess Biosyst Eng. 38: 421-8. PMID: 25199811
  7. Enzymes for pharmaceutical and therapeutic applications.  |  Meghwanshi, GK., et al. 2020. Biotechnol Appl Biochem. 67: 586-601. PMID: 32248597
  8. Fungal lipases as biocatalysts: A promising platform in several industrial biotechnology applications.  |  Mahfoudhi, A., et al. 2022. Biotechnol Bioeng. 119: 3370-3392. PMID: 36137755
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

DL-2-Amino-2-thiazoline-4-carboxylic acid, 1 g

sc-285456
1 g
$221.00

DL-2-Amino-2-thiazoline-4-carboxylic acid, 5 g

sc-285456A
5 g
$856.00