ChemicalBook > CAS DataBase List > E6005

E6005

Product Name
E6005
CAS No.
947620-48-6
Chemical Name
E6005
Synonyms
E6005;CS-2517;RVT-501;lotamilast;E 6005;E-6005;RVT-501 E6005;E 6005: RVT-501;Lotamilast (RVT501;Lotamilast, 10 mM in DMSO;Lotamilast (RVT-501) ,S0190
CBNumber
CB73170286
Molecular Formula
C26H24N4O5
Formula Weight
472.49
MOL File
947620-48-6.mol
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E6005 Property

storage temp. 
Store at -20°C
solubility 
DMSO:25.0(Max Conc. mg/mL);52.9(Max Conc. mM)
form 
A solid
color 
Light yellow to yellow
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H303May be harmfulif swallowed

H320Causes eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P312Call a POISON CENTER or doctor/physician if you feel unwell.

P337+P313IF eye irritation persists: Get medical advice/attention.

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N-Bromosuccinimide Price

Cayman Chemical
Product number
30203
Product name
E6005
Packaging
5mg
Price
$95
Updated
2024/03/01
Cayman Chemical
Product number
30203
Product name
E6005
Packaging
25mg
Price
$384
Updated
2024/03/01
Cayman Chemical
Product number
30203
Product name
E6005
Packaging
1mg
Price
$36
Updated
2024/03/01
Cayman Chemical
Product number
30203
Product name
E6005
Packaging
10mg
Price
$172
Updated
2024/03/01
TRC
Product number
R800003
Product name
RVT501
Packaging
2.5mg
Price
$65
Updated
2021/12/16
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E6005 Chemical Properties,Usage,Production

Description

E6005 is an inhibitor of phosphodiesterase 4 (PDE4; IC50 = 2.8 nM). It is selective for PDE4 over PDE1, PDE2, PDE3, and PDE5 with only 46.1, 51.6, 69.4, and 57.4% inhibition, respectively, at 30 μM. It inhibits the production of various cytokines in isolated human lymphocytes and monocytes (IC50s = 0.49-3.1 nM). Topical application of E6005 (0.003-0.3%) reduces ear thickness in a mouse model of oxazolone-induced skin inflammation, as well as reduces oxazolone-induced scratching in mice. It reduces the severity of skin lesions in a model of mite-induced atopic dermatitis. Topical application of E6005 (0.03%) also inhibits the production of leukotriene B4 (LTB4; ) in mouse skin, as well as reduces scratching and cutaneous nerve firing induced by the proteinase-activated receptor 2 (PAR2) agonist SLIGRL-NH2 in mice.

Uses

RVT 501 is a potent and selective inhibitor of human phosphodiesterase 4 (PDE4).

in vivo

Lotamilast is currently in phase 2 development for patients with mild-to-moderate atopic dermatitis. In mice models, the topical application of Lotamilast produces an immediate antipruritic effect as well as an anti-inflammatory effect with reduced expression of cytokines/adhesion molecules. On the basis of these observed effects, topical RVT-501 ameliorates the appearance of atopic dermatitis-like skin lesions in two types of AD models, hapten- and mite-elicited models, exhibiting inhibitory effects comparable to that of tacrolimus[1]. A single topical application of Lotamilast significantly inhibits spontaneous scratching during 1–2 h after application in mice with chronic dermatitis; the inhibition is partial and similar between 0.01% and 0.03%. Topical application of 0.03% Lotamilast to the rostral back significantly inhibits the increased activity of the cutaneous nerve in mice with chronic dermatitis. The cutaneous concentration of cAMP is significantly decreased in mice with chronic dermatitis, and this decrease is reversed by topical Lotamilast application[2].

References

[1] NAOTO ISHII. Antipruritic effect of the topical phosphodiesterase 4 inhibitor E6005 ameliorates skin lesions in a mouse atopic dermatitis model.[J]. Journal of Pharmacology and Experimental Therapeutics, 2013, 346 1: 105-112. DOI: 10.1124/jpet.113.205542
[2] TSUGUNOBU ANDOH  Yasushi K. Antipruritic mechanisms of topical E6005, a phosphodiesterase 4 inhibitor: Inhibition of responses to proteinase-activated receptor 2 stimulation mediated by increase in intracellular cyclic AMP[J]. Journal of dermatological science, 2014, 76 3: Pages 206-213. DOI: 10.1016/j.jdermsci.2014.10.005

E6005 Preparation Products And Raw materials

Raw materials

Preparation Products

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E6005 Suppliers

MedChemexpress LLC
Tel
021-58955995
Fax
609-228-5909
Email
sales@medchemexpress.cn
Country
United States
ProdList
4861
Advantage
58
InvivoChem
Tel
+1-708-310-1919 +1-13798911105
Fax
708-557-7486
Email
sales@invivochem.cn
Country
United States
ProdList
6391
Advantage
58
Cckinase, Inc.
Tel
+1 (732)236-3202
Email
sales@cckinase.com
Country
United States
ProdList
2738
Advantage
58
Aladdin Scientific
Tel
Email
tp@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354;
Email
support@targetmol.com
Country
United States
ProdList
39035
Advantage
58
United States Biological
Tel
--
Fax
--
Email
sales@advtechind.com
Country
United States
ProdList
6075
Advantage
58
Cayman Chemical Company
Tel
--
Fax
--
Email
cayman@caymanchem.com
Country
United States
ProdList
6213
Advantage
81
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
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View Lastest Price from E6005 manufacturers

ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
Product
E6005 947620-48-6
Price
US $2.00-6.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
100kg
Release date
2025-07-29

947620-48-6, E6005Related Search:


  • E6005
  • RVT-501
  • lotamilast
  • E 6005: RVT-501
  • METHYL 4-((3-(6,7-DIMETHOXY-2-(METHYLAMINO)QUINAZOLIN-4-YL)PHENYL)CARBAMOYL)BENZOATE
  • RVT-501 E6005
  • methyl 4-[({3-[6,7-dimethoxy-2-(methylamino)quinazolin-4-yl]phenyl}amino)carbonyl]benzoate
  • CS-2517
  • E 6005;E-6005
  • Benzoic acid, 4-[[[3-[6,7-dimethoxy-2-(methylamino)-4-quinazolinyl]phenyl]amino]carbonyl]-, methyl ester
  • Lotamilast (RVT501
  • RVT501,Lotamilast,E 6005,RVT 501,E-6005,Inhibitor,Phosphodiesterase (PDE),inhibit
  • Lotamilast, 10 mM in DMSO
  • Lotamilast (RVT-501) ,S0190
  • 947620-48-6