TETRACYCLINE

Tetracycline inhibits bacterial protein synthesis via the 30S ribosomal subunit. Used for respiratory and skin infections. Side effects include GI upset, photosensitivity, tooth discoloration, and hepatotoxicity.

SKU: e611524fa2c3 Category: Tag:

Product Description


Mechanism of Action

TETRACYCLINE (ID 27613) demonstrates a broad and highly integrated biochemical activity architecture involving multi‑axis signalling interference, mitochondrial-network recalibration, catalytic‑domain modulation, cytoskeletal restructuring, redox‑equilibrium shaping, ion‑flux redistribution and transcription‑factor pathway realignment. Its molecular geometry allows docking to catalytic residues, allosteric regulators, hydrophobic transmembrane helices, nucleotide‑binding pockets, structural scaffolds and polymeric cytoskeletal networks. This enables TETRACYCLINE to influence metabolic, structural, genomic, electrophysiological and stress‑adaptive systems simultaneously.

TETRACYCLINE may modulate phosphorylation gradients, modify ERK/JNK/MAPK propagation speeds, influence PI3K–AKT survival bias, shift G‑protein signalling states, control Ca²⁺ microdomain behaviour, alter IP₃/DAG cascades, and recalibrate cAMP‑PKA pathway amplitude. Mitochondrial impacts include ETC‑complex redistribution, ATP/ADP cycle reshaping, ROS‑threshold displacement, membrane‑potential polarity changes and organelle‑stress cross‑signalling.

High‑Precision Research Applications

  • Ultra‑scale kinome disruption & catalytic‑cascade modelling
  • Molecular docking & conformational‑flow prediction
  • UPR/ER‑stress and mitophagy/autophagy integration research
  • Full‑spectrum multi‑omics reconstruction (RNA‑seq, metabolomics, phosphoproteomics)
  • Advanced cytoskeletal force‑distribution & polymer‑turnover analysis
  • Cell‑fate simulation across apoptosis, ferroptosis, necroptosis & parthanatos
  • AI‑enhanced SAR/QSAR simulation for molecular optimisation

Toxicodynamics & Hazard Spectrum

  • Rapid ROS escalation & antioxidant‑buffer collapse
  • Mitochondrial fragmentation or ETC suppression
  • Severe Ca²⁺/Na⁺/K⁺ ion‑flux destabilisation
  • Cytoskeletal polymer breakdown & structural‑integrity failure
  • Membrane rupture & lipid‑bilayer thinning
  • Overactivation of inflammatory cascades (NF‑κB, STAT, IRF)
  • Activation of multiple programmed‑cell‑death pathways
  • Epigenetic drift including methylation instability

For expert laboratory use only — not intended for biological exposure.

Datasheet


Molecular Formula

C22H24N2O8

Molecular Weight

444.4 g/mol

CAS Number

60-54-8

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance.

Purity

Purity information is available upon request (COA).

Synonym

tetracycline; 60-54-8; Deschlorobiomycin; Tsiklomitsin; Tetraciclina

IUPAC/Chemical Name

(4S,4aS,5aS,6S,12aR)-4-(dimethylamino)-1,6,10,11,12a-pentahydroxy-6-methyl-3,12-dioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide

InChl Key

NWXMGUDVXFXRIG-WESIUVDSSA-N

InChl Code

InChI=1S/C22H24N2O8/c1-21(31)8-5-4-6-11(25)12(8)16(26)13-9(21)7-10-15(24(2)3)17(27)14(20(23)30)19(29)22(10,32)18(13)28/h4-6,9-10,15,25-26,29,31-32H,7H2,1-3H3,(H2,23,30)/t9-,10-,15-,21+,22-/m0/s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/54675776;

3D Conformer.

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