ChemicalBook >> CAS DataBase List >>16,16-DIMETHYL PROSTAGLANDIN E2

16,16-DIMETHYL PROSTAGLANDIN E2

CAS No.
39746-25-3
Chemical Name:
16,16-DIMETHYL PROSTAGLANDIN E2
Synonyms
15r)-13e;opentyl)-;16-dimethyl PGE2;16,16-dimethyl-pge2;16,16-Dimethyl dinoprostone;QAOBBBBDJSWHMU-WMBBNPMCSA-N;Suppliedasayellow,viscousoil;16-Dimethyl prostaglandin E2;16,16-DimethylprostaglandineE2;16,16-DIMETHYL PROSTAGLANDIN E2
CBNumber:
CB9416741
Molecular Formula:
C22H36O5
Molecular Weight:
380.52
MDL Number:
MFCD00151141
MOL File:
39746-25-3.mol
Last updated:2023-06-30 15:45:59

16,16-DIMETHYL PROSTAGLANDIN E2 Properties

Flash point -13℃
storage temp. -20°C
solubility Soluble in methyl acetate
form methyl acetate solution
FDA UNII M790V82VAC
NCI Drug Dictionary 16, 16-dimethyl prostaglandin E2

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07
Signal word  Danger
Hazard statements  H225-H319-H336
Precautionary statements  P210-P305+P351+P338
Hazard Codes  F,Xn,Xi
Risk Statements  11-20/21/22-36/37/38-67-66-36
Safety Statements  16-26-36
RIDADR  UN 1231 3/PG 2
WGK Germany  3
NFPA 704
3
2 0

16,16-DIMETHYL PROSTAGLANDIN E2 price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich D0160 16,16-Dimethylprostaglandin E2 methyl acetate solution 39746-25-3 1mg $348 2023-06-20 Buy
Cayman Chemical 14750 16,16-dimethyl Prostaglandin E2 ≥98% 39746-25-3 1mg $86 2024-03-01 Buy
Cayman Chemical 14750 16,16-dimethyl Prostaglandin E2 ≥98% 39746-25-3 5mg $399 2024-03-01 Buy
Cayman Chemical 14750 16,16-dimethyl Prostaglandin E2 ≥98% 39746-25-3 10mg $755 2024-03-01 Buy
Tocris 4027 16,16-Dimethylprostaglandin E2 ≥98%(HPLC) 39746-25-3 1 $125 2021-12-16 Buy
Product number Packaging Price Buy
D0160 1mg $348 Buy
14750 1mg $86 Buy
14750 5mg $399 Buy
14750 10mg $755 Buy
4027 1 $125 Buy

16,16-DIMETHYL PROSTAGLANDIN E2 Chemical Properties,Uses,Production

Description

16,16-dimethyl PGE2 is a competitive inhibitor of 15-hydroxy PGDH, but it is not a substrate for the enzyme. Because of its resistance to metabolism by 15-hydroxy PGDH, it has a prolonged half-life in vivo. 16,16-dimethyl PGE2 acts as an agonist on most EP receptor subtypes, and has been used experimentally to induce cervical ripening, uterine contraction, and prevent ulceration of the gastric mucosa in rats and dogs. The Kd for activation of isolated EP2 receptors is about 1 nM. 16,16-dimethyl PGE2 can be used to preserve the self-renewal properties while preventing the differentiation of hematopoietic stem cells during expansion in culture.

Definition

ChEBI: 16,16-dimethylprostaglandin E2 is a prostanoid that is prostaglandin E2 in which both of the hydrogens at position 16 have been replaced by methyl groups. A synthetic analogue of prostaglandin E2, it is a potent inhibitor of pancreatic function and growth of experimental tumors. It also protects the gastric mucosa, prevents ulceration, and promotes the healing of peptic ulcers. It has a role as a radiation protective agent, an anti-ulcer drug and a gastrointestinal drug. It is a prostanoid, a monocarboxylic acid, a secondary allylic alcohol and a member of cyclopentanones.

in vitro

dmpge2 was reported to cause an increase in runx11/cmyb1 hscs, while hscs were inhibited by indomethacin treatment in 90% of embryos. moreover, dmpge2 had minimal effects on the vasculature, while indomethacin altered the intersomitic vessels slightly. imaged by confocal microscopy, red-labelled hscs and endothelium embryos showed significantly increased hscs following dmpge2 exposure [1].

in vivo

in a heterotopic model of rat allograft rejection, dmpge2 could delay the rejection onset, but all animals developed severe rejection and died subsequently. treatment of animals with low-dose csa in combination with dmpge2 led to a delay in the onset as well as a reduction in the intensity of allograft rejection. in addition, a statistical relationship between procoagulant activity levels and the time of onset of rejection was observed [1].

storage

Store at -80°C

References

[1] north te,goessling w,walkley cr,lengerke c,kopani kr,lord am,weber gj,bowman tv,jang ih,grosser t,fitzgerald ga,daley gq,orkin sh,zon li. prostaglandin e2 regulates vertebrate haematopoietic stem cell homeostasis. nature.2007 jun 21;447(7147):1007-11.
[2] koh ih,kim pc,chung sw,waddell t,wong py,gorczynski r,levy ga,cohen z. the effects of 16, 16 dimethyl prostaglandin e2 therapy alone and in combination with low-dose cyclosporine on rat small intestinal transplantation. transplantation.1992 oct;54(4):592-8.

42782-96-7
39746-25-3
Synthesis of 16,16-DIMETHYL PROSTAGLANDIN E2 from Prosta-5,13-dien-1-oic acid, 11,15-dihydroxy-16,16-dimethyl-9-oxo-, methyl ester, (5Z,11α,13E,15R)- (9CI)

16,16-DIMETHYL PROSTAGLANDIN E2 Preparation Products And Raw materials

16,16-DIMETHYL PROSTAGLANDIN E2 Suppliers

Global( 54)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Shanghai Acmec Biochemical Technology Co., Ltd.
+undefined18621343501 product@acmec-e.com China 33349 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 52927 58
3B Pharmachem (Wuhan) International Co.,Ltd. 821-50328103-801 18930552037 3bsc@sina.com China 15848 69
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51471 80
EMMX Biotechnology LLC 888-539-0666 info@emmx.com United States 8449 60
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9709 58
Hangzhou Synstar pharmaceutical Technology CO.,Ltd 0571-85361029 synstar518@163.com China 1991 58
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11289 58
Energy Chemical 021-58432009 400-005-6266 marketing1@energy-chemical.com China 44894 58
16,16-DIMETHYL PROSTAGLANDIN E2 (5z,11-alpha,13e,15r)-11,15-dihydroxy-16,16-dimethyl-9-oxoprosta-5,13-dien-1 15r)-13e 16,16-dimethyl-pge2 5-heptenoicacid,7-(2-(4,4-dimethyl-3-hydroxy-1-octenyl)-3-hydroxy-5-oxocycl opentyl)- prosta-5,13-dien-1-oicacid,11,15-dihydroxy-16,16-dimethyl-9-oxo-,(5z,11-alph 16,16-DimethylprostaglandineE2 Suppliedasayellow,viscousoil 16,16-DIMETHYL PROSTAGLANDIN E2 SUPPLIED AS A YELLOW, VISCOUS OIL (5Z,13E,15R)-11α,15-Dihydroxy-16,16-dimethyl-9-oxoprosta-5,13-dien-1-oic acid 16,16-Dimethyl dinoprostone (5Z,11α,13E,15R)-11,15-Dihydroxy-16,16-dimethyl-9-oxo-prosta-5,13-dien-1oicacid 9-OXO-11ALPHA,15R-DIHYDROXY-16,16-DIMETHYL-PROSTA-5Z,13E-DIEN-1-OIC ACID QAOBBBBDJSWHMU-WMBBNPMCSA-N Prosta-5,13-dien-1-oic acid, 11,15-dihydroxy-16,16-dimethyl-9-oxo-, (5Z,11α,13E,15R)- 16,16-Dimethylprostaglandin E2 methyl acetate solution 16-dimethyl PGE2 16-Dimethyl prostaglandin E2 16,16 Dimethyl prostaglandin E2,16,16Dimethyl prostaglandin E2,16,16-Dimethyl prostaglandin E-2 (5Z,11α,13E,15R)-11,15-Dihydroxy-16,16-diMethyl-9-oxo-prosta-5,13-dien-1oicacid 16,16-Dimethylprostaglandin E2, 15-hydroxy PGDH inhibitor 39746-25-3 C22H36O5 Biochemicals and Reagents Lipids Fatty Acids Prostaglandins BioChemical Fatty Acids Lipids Prostaglandins