Date published: 2026-2-8

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5-(5-Bromo-2-furyl)-4-propyl-4H-1,2,4-triazole-3-thiol

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Molecular Weight:
288.16
Molecular Formula:
C9H10BrN3OS
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Manumycin A is an antibiotic originally generated by Streptomyces parvulus that acts as a selective and vigorous inhibitor of Ras farnesyltransferase. The compound has been observed to block the activity of IKKbeta by robustly and rapidly inhibiting TNF alpha induced phosphorylation of IkappaBalpha and NF-kappaB nuclear translocation. Studies indicate that Manumycin A has the ability to induce the dimerization of IKKbeta and dissociation of IKK from IKKgamma/NEMO, the adapter protein. Atherosclerosis studies report that Manumycin A decreases oxidative stress. Additionally, Manumycin A irreversibly inhibits neutral sphingomyelina, and may act to produce nitric oxide and induce apoptosis in leukemia cell studies. Manumycin A is an inhibitor of Farnesyl Transferase and N-SMase.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

5-(5-Bromo-2-furyl)-4-propyl-4H-1,2,4-triazole-3-thiol, 500 mg

sc-317706
500 mg
$180.00