Date published: 2025-10-18

1-800-457-3801

SCBT Portrait Logo
Seach Input

Porphine (CAS 101-60-0)

0.0(0)
Write a reviewAsk a question

Application:
Porphine is a parent compound for many porphyrins
CAS Number:
101-60-0
Molecular Weight:
310.35
Molecular Formula:
C20H14N4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Porphine, an aromatic heterocycle, serves as a building block for various porphyrins, including heme, and exhibits the ability to form metal complexes through its central nitrogen atoms. As an organic compound within the porphyrin family, porphine holds significant importance in the composition of heme, a vital cofactor found in proteins like hemoglobin. Comprised of four pyrrole rings interconnected by methine bridges, porphine exists as a colorless solid and demonstrates solubility in most organic solvents. Extensively investigated in biochemistry and pharmacology, porphine has contributed to the exploration of hemoglobin′s structure, function, and its role in cellular respiration and energy generation. Furthermore, studies involving porphine have shed light on the structure, function, and synthesis of proteins involved in heme biosynthesis and other biomolecules. Acting as a cofactor, porphine engages in oxidation-reduction reactions within hemoglobin and other heme-related proteins. By binding to the heme prosthetic group, it facilitates electron transfer between the iron atom and the heme prosthetic group, enabling essential energy-producing oxidation-reduction reactions to take place.


Porphine (CAS 101-60-0) References

  1. Determination of iron-porphyrin-like complexes at nanomolar levels in seawater.  |  Vong, L., et al. 2007. Anal Chim Acta. 588: 237-44. PMID: 17386816
  2. Strategies for development of antimalarials based on encapsulated porphyrin derivatives.  |  Deda, DK., et al. 2015. Mini Rev Med Chem. 14: 1055-71. PMID: 25553431
  3. β-Formyl- and β-Vinylporphyrins: Magic Building Blocks for Novel Porphyrin Derivatives.  |  Cerqueira, AFR., et al. 2017. Molecules. 22: PMID: 28758915
  4. Advancing porphyrin's biomedical utility via supramolecular chemistry.  |  Rajora, MA., et al. 2017. Chem Soc Rev. 46: 6433-6469. PMID: 29048439
  5. Antibacterial activity of porphyrin derivatives against multidrug-resistant bacteria.  |  Tasli, H., et al. 2019. Pak J Pharm Sci. 32: 2369-2373. PMID: 31894020
  6. Classic highlights in porphyrin and porphyrinoid total synthesis and biosynthesis.  |  Senge, MO., et al. 2021. Chem Soc Rev. 50: 4730-4789. PMID: 33623938
  7. Porphyrin in Prebiotic Catalysis: Ascertaining a Route for the Emergence of Early Metalloporphyrins.  |  Dagar, S., et al. 2022. Chembiochem. 23: e202200013. PMID: 35233914

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Porphine, 5 mg

sc-264082
5 mg
$235.00

Porphine, 10 mg

sc-264082A
10 mg
$454.00