JavaScript is disabled in your browser. Please enable JavaScript to view this website.
AB141282

Dienogest, Steroidal progesterone

Be the first to review this product! Submit a review

|

(1 Publication)

MW 311.4 Da, Purity >99%. Steroidal progesterone. Non-ethinylated progestin structurally related to testosterone. Anti-androgenic and antiproliferative effects in vitro.
2 Images
Functional Studies - Dienogest, Steroidal progesterone (AB141282)
  • FuncS

Unknown

Functional Studies - Dienogest, Steroidal progesterone (AB141282)

ab16895 staining MDM2 in MCF7 cells treated with dienogest (ab141282), by ICC/IF. Decrease in MDM2 expression correlates with increased concentration of dienogest, as described in literature.
The cells were incubated at 37°C for 24 hour in media containing different concentrations of ab141282 (dienogest) in DMSO, fixed with 4% formaldehyde for 10 minutes at room temperature and blocked with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% tween for 2h at room temperature. Staining of the treated cells with ab16895 (5 µg/ml) was performed overnight at 4°C in PBS containing 1% BSA and 0.1% tween. A DyLight® 488 anti-mouse polyclonal antibody (ab96879) at 1/250 dilution was used as the secondary antibody. Nuclei were counterstained with DAPI and are shown in blue.

Chemical Structure - Dienogest, Steroidal progesterone (AB141282)
  • Chemical Structure

Lab

Chemical Structure - Dienogest, Steroidal progesterone (AB141282)

2D chemical structure image of ab141282, Dienogest, Steroidal progesterone

Key facts

CAS number

65928-58-7

Purity

>99%

Form

Solid

form

Molecular weight

311.4 Da

Molecular formula

C<sub>2</sub><sub>0</sub>H<sub>2</sub><sub>5</sub>NO<sub>2</sub>

PubChem

68861

Nature

Synthetic

Solubility

Soluble in DMSO to 100 mM

Biochemical name

Dienogest

Biological description

Steroidal progesterone. Non-ethinylated progestin structurally related to testosterone. Anti-androgenic and antiproliferative effects in vitro.

Canonical smiles

CC12CCC3=C4CCC(=O)C=C4CCC3C1CCC2(CC#N)O

Isomeric smiles

C[C@]12CCC3=C4CCC(=O)C=C4CC[C@H]3[C@@H]1CC[C@]2(CC#N)O

InChi

InChI=1S/C20H25NO2/c1-19-8-6-16-15-5-3-14(22)12-13(15)2-4-17(16)18(19)7-9-20(19,23)10-11-21/h12,17-18,23H,2-10H2,1H3/t17-,18+,19+,20-/m1/s1

InChiKey

AZFLJNIPTRTECV-FUMNGEBKSA-N

IUPAC Name

2-[(8S,13S,14S,17R)-17-hydroxy-13-methyl-3-oxo-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-17-yl]acetonitrile

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
Store under desiccating conditions|The product can be stored for up to 12 months

Product protocols

Publications (1)

Recent publications for all applications. Explore the full list and refine your search

Fertility and sterility 104:655-64.e1 PubMed26051103

2015

Dienogest enhances autophagy induction in endometriotic cells by impairing activation of AKT, ERK1/2, and mTOR.

Applications

Unspecified application

Species

Unspecified reactive species

JongYeob Choi,MinWha Jo,EunYoung Lee,Dong-Yun Lee,DooSeok Choi
View all publications

Product promise

We are committed to supporting your work with high-quality reagents, and we're here for you every step of the way. In the unlikely event that one of our products does not perform as expected, you're protected by our Product Promise.
For full details, please see our Terms & Conditions

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

For licensing inquiries, please contact partnerships@abcam.com