15-deoxy-Δ12,14-Prostaglandin A1 • 15-<wbr/>deoxy-<wbr/>Δ<sup>12,14</sup>-<wbr/>PGA<sub>1</sub> (CAS 573951-20-9) (Inchi key LDOCIRJMPUHXRM-YUJGFSRTSA-N) || Cayman Chemical | Supplier
15-deoxy-Δ12,14-Prostaglandin A1
Item № 10065
CAS № 573951-20-9
Purity ≥95%
product image
SIZE PRICE QUANTITY SUBTOTAL
CART TOTAL $0.00
500 µg $78.00 $0.00
1 mg $117.00 $0.00
5 mg $546.00 $0.00

Pricing updated 2015-09-02. Prices are subject to change without notice.

Bulk Inquiry Form

X

Enter number, size, and select unit. Example: 2 x 500 mg

Please indicate any analytical testing requirements, special handling, packaging, or delivery requirements.

Description
Synonyms
  • 15-deoxy-Δ12,14-PGA1

15-deoxy-Δ12,14-Prostaglandin A1 (15-deoxy-Δ12,14-PGA1) is a synthetic PGA1 analog. It shares common structural features with 15-deoxy-Δ12,14-PGJ2, which is a ligand for PPARγ.1 Antimitotic and antitumor activity have been reported for a similar analog, but there are no published reports on the biological activity of 15-deoxy-Δ12,14-PGA1 at this time.2

Download Product Insert Download Safety Data Sheet (SDS)

Related Products

Show all 4 Hide all but first 3

View Related Product Categories
View Screening Libraries with 15-deoxy-Δ12,14-Prostaglandin A1
Technical Information
Formal Name 9-​oxo-​prosta-​10,​12Z,​14E-​trien-​1-​oic acid
CAS Number 573951-20-9
Synonyms
  • 15-deoxy-Δ12,14-PGA1
Molecular Formula C20H30O3
Formula Weight 318.5
Purity ≥95%
Formulation A solution in methyl acetate
λmax 324 nm
SMILES CCCCC/C=C/C=C1\C=CC(=O)​C\1CCCCCCC(=O)​O
InChI Code ​1S/C20H30O3/c1-2-3-4-5-6-9-12-17-15-16-19(21)​18(17)​13-10-7-8-11-14-20(22)​23/h6,9,12,15-16,18H,2-5,7-8,10-11,13-14H2,1H3,(H,22,23)​/b9-6+,17-12-/t18-/m1/s1
InChI Key LDOCIRJMPUHXRM-YUJGFSRTSA-N

WARNING - This product is not for human or veterinary use.

Shipping & Storage
Storage -80°C
Shipping Dry ice in continental US; may vary elsewhere
Stability 1 year
Product Downloads & Resources
Product Downloads

Download Product Insert 207 Kb PDF

Download Safety Data Sheet (SDS) 30 Kb PDF

Download free InChI Key generation software

Additional Information

View the Cayman Structure Database for chemical structure definitions for many Cayman products

Get Batch-Specific Data and Documents by Batch Number

Separate multiple batch numbers with commas

Inserts
QC Sheets
Certificates of Analysis
GCMS Data
References & Background Reading
Product Description References

1. Kliewer, S.A., Lenhard, J.M., Willson, T.M., et al. A prostaglandin J2 metabolite binds peroxisome proliferator-activated receptor γ and promotes adipocyte differentiation. Cell 83 813-819 (1995).

2. Kato, T., Fukushima, M., Kurozumi, S., et al. Antitumor activity of Δ7-prostaglandin A1 and Δ12-prostaglandin J2 in vitro and in vivo. Cancer Res 46 3538-3542 (1986).

Technical Support
Contact Us
  • To streamline the process attach the appropriate questionnaire to your inquiry.

  • Toll Free Phone (USA and Canada Only): (888) 526-5351
  • Direct Phone: (734) 975-3888
Contract Research Services

We offer you the deep and diverse knowledge of more than 100 in-house scientists and the expertise that comes from more than three decades of designing and developing the tools to advance biomedical research.

Cayman is know as a partner to scientists worldwide, responding to your needs with services in:

Cayman Chemical

1180 East Ellsworth Road

Ann Arbor, Michigan 48108 USA

JOIN OUR SOCIAL NETWORK!

Please wait...