[CAS NO. 3963-95-9]  Methacyclinehydrochloride

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PRODUCTS SPECIFICATIONS [3963-95-9]

Catalog
AS393563
Brand
Arctom Scientific
CAS
3963-95-9

DESCRIPTION [3963-95-9]

Overview

MDLMFCD04972012
Molecular Weight478.88
Molecular FormulaC22H23ClN2O8
SMILESO[C@@](C(O)=C(C(C1=C2C=CC=C1O)=O)[C@](C2=C)([H])[C@@H]3O)(C(C(C(N)=O)=C4O)=O)[C@]3([H])[C@@H]4N(C)C.Cl

For research use only. We do not sell to patients.


Summary

Methacycline hydrochloride is a tetracycline antibiotic and can inhibits bacterial protein synthesis. Methacycline hydrochloride is a potent epithelial-mesenchymal transition (EMT) inhibitor. Methacycline hydrochloride blocks EMT in vitro and fibrogenesis in vivo without directly affecting TGF-β1 Smad signaling. Methacycline hydrochloride is an antimicrobial and has the potential for pulmonary fibrosis [1] .


IC50 & Target

Tetracycline


In Vitro

Methacycline hydrochloride is an inhibitor of A549 EMT with an IC50 of roughly 5 μM [1] .
In vitro, Methacycline hydrochloride (10, 20 μM; for 48 hours) inhibits TGF-β1-induced α-smooth muscle actin, Snail1, and collagen I of primary alveolar epithelial cells. Methacycline hydrochloride inhibits TGF-β1–induced non-Smad pathways, including c-Jun N-terminal kinase, p38, and Akt activation, but not Smad or β-catenin transcriptional activity. Methacycline has no effect on baseline c-Jun N-terminal kinase, p38, or Akt activities or lung fibroblast responses to TGF-β1 [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


In Vivo

In vivo, Methacycline hydrochloride (100 mg/kg/day; ip; beginning 10 days after intratracheal Bleomycin) improves survival at Day 17. Bleomycin-induced canonical EMT markers, Snail1, Twist1, collagen I, as well as fibronectin protein and mRNA, ARE attenuated by Methacycline hydrochloride (Day 17) [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

4°C, sealed storage, away from moisture

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)


Solvent & Solubility

In Vitro:

DMSO : 50 mg/mL ( 104.41 mM ; Need ultrasonic)

H 2 O : 6.67 mg/mL ( 13.93 mM ; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.0882 mL 10.4410 mL 20.8821 mL
5 mM 0.4176 mL 2.0882 mL 4.1764 mL
10 mM 0.2088 mL 1.0441 mL 2.0882 mL
* Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one: 10% DMSO >> 90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.5 mg/mL (5.22 mM); Clear solution

* All of the co-solvents are available by MCE.


Synonyms

2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methylene-1,11-dioxo-, hydrochloride (1:1), (4S,4aR,5S,5aR,12aS)-
2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methylene-1,11-dioxo-, monohydrochloride
2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methylene-1,11-dioxo-, monohydrochloride, [4S-(4α,4aα,5α,5aα,12aα)]-
2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methylene-1,11-dioxo-, monohydrochloride, (4S,4aR,5S,5aR,12aS)-
6-Demethyl-6-deoxy-6-methyleneoxytetracycline monohydrochloride
Methacycline monohydrochloride
Methacycline hydrochloride
6-Methylene-5-hydroxytetracycline chlorohydrate
6-Methylene-5-hydroxytetracycline hydrochloride
6-Demethyl-6-deoxy-6-methylene-5-hydroxytetracycline hydrochloride
Metacycline hydrochloride
6-Methyleneoxytetracycline hydrochloride
6-Demethyl-6-deoxy-5-hydroxy-6-methylenetetracycline hydrochloride
Metacyclin hydrochloride
Rindex
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Physiomycine
Metilenbiotic
Metadomus
Ciclobiotic
Londomycin
Germiciclin
Optimycin