Chemodex

Doxycycline hyclate

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Product Details
Synonyms Doxycycline hydrochloride hemiethanolate hemihydrate; α-6-Deoxy-5-hydroxytetracycline; Vibramycin hyclate
Product Type Chemical
Properties
Formula C22H24N2O8 . HCl . 0.5H2O . 0.5C2H6O
MW 512.94
CAS 24390-14-5
RTECS QI8925000
Source/Host Chemicals Synthetic
Purity Chemicals ≥98% (HPLC)
Appearance Yellow powder.
Solubility Soluble in water (5mg/ml).
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturer's product datasheet.

InChi Key HALQELOKLVRWRI-ZVACAFRPSA-N
Smiles OC1=C2C([C@H](C)C3C(C2=O)=C(O)[C@@]4(O)C([C@H](N(C)C)C(O)=C(C(N)=O)C4=O)[C@H]3O)=CC=C1.CCO.OC5=C6C([C@H](C)C7C(C6=O)=C(O)[C@@]8(O)C([C@H](N(C)C)C(O)=C(C(N)=O)C8=O)[C@H]7O)=CC=C5.Cl.O.Cl
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
Product Specification Sheet
Datasheet Download PDF
Description
Doxycycline hyclate is a broad-spectrum tetracycline antibiotic. It binds to the 30S ribosomal subunit of bacteria and inhibits protein synthesis, preventing bacteria from growing and replicating. Next to its antibacterial activity it shows also anti-inflammatory, anti-protozoal, neuroprotective, anti-viral and anti-cancer properties. Doxycycline also inhibits selective human matrix metalloproteinases (MMP-8, MMP-9, MMP-13), inhibits replication of some viruses, inhibits the apicoplast of the malaria parasite Plasmodium spp. and reduces neuoinflammation. It can be used as a regulator for inducible gene expression systems where expression depends on either the presence (Tet-On) or absence (Tet-Off) of doxycycline. Intermediate for the synthesis of fluorescent probes.
Product References
(1) G.M. Williamson; Chemotherapia 13, 1 (1968) | (2) I. Chopra; Antimicrob. Agents Chemother. 38, 637 (1994) | (3) G.N. Smith, et al.; Arthritis Rheum. 42, 1140 (1999) | (4) D.J. Gould, et al.; Gene Ther. 7, 2061 (2000) | (5) B.A. Cunha; Med. Clin. North Am. 90, 1089 (2006) | (6) B. Berman, et al.; Drugs Today 43, 27 (2007) | (7) J. Sagar, et al.; Anticancer Agents Med. Chem. 10, 556 (2010) | (8) M.O. Griffin, et al.; Pharmacol. Res. 63, 102 (2011) | (9) A.T. Das, et al.; Curr. Gene Ther. 16, 156 (2016) | (10) C. Balducci & G. Forloni; Front. Pharmacol. 10, 738 (2019) | (11) F. Chi, et al.; Virus Res. 345, 199388 (2024)
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