D9891

Doxycycline hyclate

Manufacturer: Sigma Aldrich

CAS Number: 24390-14-5

Synonym(S): 6-Desoxy-5-hydroxytetracycline hydrochloride hemihydrate hemiethanolate, Doxycycline hydrochloride hemiethanolate hemihydrate

Select a Size

Pack Size SKU Availability Price
1 G D9891-1-G In Stock ₹ 6,094.48
5 G D9891-5-G In Stock ₹ 18,056.10
10 G D9891-10-G In Stock ₹ 23,501.08
25 G D9891-25-G In Stock ₹ 30,959.50
100 G D9891-100-G In Stock ₹ 1,20,157.50

D9891 - 1 G

₹ 6,094.48

In Stock

Quantity

1

Base Price: ₹ 6,094.48

GST (18%): ₹ 1,097.006

Total Price: ₹ 7,191.486

biological source

synthetic

Quality Level

200

Assay

≥93.5% (HPLC)95.0-102.0% anhydrous basis (ethanol free based)

form

powder

storage condition

(Tightly closed. Dry. )

color

yellow to yellow-green

antibiotic activity spectrum

Gram-negative bacteriaGram-positive bacteriamycoplasmaparasites

Mode of action

protein synthesis | interferes

storage temp.

2-8°C

SMILES string

Cl[H].Cl[H].[H]O[H].CCO.C[C@@H]1C2[C@H](O)C3[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]3(O)C(O)=C2C(=O)c4c(O)cccc14.C[C@@H]5C6[C@H](O)C7[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]7(O)C(O)=C6C(=O)c8c(O)cccc58

Other Options

Image Product Name Manufacturer Price Range
50-194-7977
Selleck Chemical LLC Doxycycline Hyclate 100mg 24390-14-5
Selleck Chemical LLC ₹ 15,092.78
50-199-8586
Apexbio Technology LLC Doxycycline hyclate, 10g Cas# 24390-14-5
Apexbio Technology LLC ₹ 7,700.40
50-200-9006
Enzo Life Sciences Doxycycline . hyclate (1g). CAS: 24390-14-5
Enzo Life Sciences ₹ 4,688.69
50-199-8585
Apexbio Technology LLC Doxycycline hyclate, 5g Cas# 24390-14-5
Apexbio Technology LLC ₹ 6,074.76
NC0233297
Enzo Life Sciences Doxycycline . hyclate, (5g), CAS Number: 24390-14-5
Enzo Life Sciences ₹ 9,347.43
11-101-2182
Doxycycline hyclate Pharmaceutical Secondary Standard, MilliporeSigma™ Supelco™
MilliporeSigma Supelco ₹ 12,799.78
50-174-7696
Sigma Aldrich Fine Chemicals Biosciences Doxycycline Hyclate | 24390-14-5 | MFCD07357237 | 200mg
Sigma Aldrich Fine Chemicals Biosciences ₹ 45,791.71
50-174-7698
Sigma Aldrich Fine Chemicals Biosciences Doxycycline hyclate | 24390-14-5 | MFCD07357237 | 100G
Sigma Aldrich Fine Chemicals Biosciences ₹ 1,69,451.58
50-174-7699
Sigma Aldrich Fine Chemicals Biosciences Doxycycline Hyclate | 24390-14-5 | MFCD07357237 | 10g
Sigma Aldrich Fine Chemicals Biosciences ₹ 25,679.12
NC1401612
U.S. Pharmacopeia Doxycycline Hyclate, 24390-14-5, MFCD07357237, 200 mg
U.S. Pharmacopeia ₹ 29,661.94

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Description

  • General description: Doxycycline Hyclate, a synthetic tetracycline antibiotic, demonstrates broad-spectrum antimicrobial activity against various bacteria by binding to the 30S and potentially the 50S ribosomal subunits. This binding disrupts the aminoacyl-tRNA binding to the mRNA-ribosome complex, effectively inhibiting bacterial protein synthesis, thereby halting growth and replication. Beyond its antimicrobial effects, Doxycycline Hyclate serves as an inhibitor of matrix metalloproteinases (MMPs), enzymes crucial for collagen breakdown in connective tissues. Studies on corneal erosion and rheumatoid arthritis showcase its significant reduction in MMP-9 and MMP-8 levels, respectively. This MMP-inhibiting property helps preserve collagen integrity, preventing excessive tissue degradation and supporting tissue repair.In cell biology, Doxycycline Hyclate impacts smooth muscle cells, enhancing adhesion and influencing the reorganization of fibrillar collagen matrices. Its influence on apicoplast gene expression in Plasmodium falciparum, the malaria-causing parasite, adds a dimension of significance in infectious disease research. Additionally, the inhibition of tissue formation in rat studies contributes to its relevance in understanding tissue development. Moreover, Doxycycline Hyclate holds potential in metabolomics research, considering its multi-faceted effects on various cellular processes. In the broader context of biochemical research, its versatile actions make it a valuable tool for investigating molecular mechanisms and signaling pathways.
  • Application: Doxycycline hyclate has been used for the induction of glioma cells[1] and human embryonic kidney 293T cells (HEK293T).[2]
  • Biochem/physiol Actions: Mode of Action: Doxycycline hyclate inhibits the inflammatory response to the Lyme Disease Spirochete Borrelia burgdorferi.Activity Spectrum: Effective against a broad spectrum inhibitor of matrix metalloproteinases in vivo.
  • Features and Benefits: High-quality antibiotic suitable for multiple research applicationsIdeal for Cell Biology, Metabolomics, and Biochemical research.
  • Other Notes: 2024 CiteAb Award Winner for Supplier Succeeding in Parkinson′s Research

SAFETY INFORMATION

Pictograms

GHS08,GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335,H361fd,H412

Precautionary Statements

P202 - P273 - P301 + P312 - P302 + P352 - P305 + P351 + P338 - P308 + P313

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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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biological source:
synthetic

Quality Level:
200

Assay:
≥93.5% (HPLC)95.0-102.0% anhydrous basis (ethanol free based)

form:
powder

storage condition:
(Tightly closed. Dry. )

color:
yellow to yellow-green

antibiotic activity spectrum:
Gram-negative bacteriaGram-positive bacteriamycoplasmaparasites

Mode of action:
protein synthesis | interferes

storage temp.:
2-8°C

SMILES string:
Cl[H].Cl[H].[H]O[H].CCO.C[C@@H]1C2[C@H](O)C3[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]3(O)C(O)=C2C(=O)c4c(O)cccc14.C[C@@H]5C6[C@H](O)C7[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]7(O)C(O)=C6C(=O)c8c(O)cccc58

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