Cyclooxygenase

Prostaglandin E1 (PGE1) is not a major naturally occurring prostaglandin, but it is widely administered clinically for several indications including peripheral occlusive vascular disease, erectile dysfunction and in neonatal cardiology.

CTA2 is a stable analog of TXA2.

6-keto Prostaglandin F1α-d4 (6-keto PGF1α-d4) contains four deuterium atoms at the 3, 3', 4, and 4' positions.

Prostaglandin A1 (PGA1) ethyl ester is a prodrug form of PGA1 with enhanced lipid solubility.

CAY10526은 특정 마이크로솜 PGE2 신타제-1(mPGES1) 억제제입니다. CAY10526은 mPGES1 발현의 선택적 조절을 통해 PGE2 생산을 억제하지만 COX-2에는 영향을 미치지 않는다. CAY10526은 흑색종 이종이식편에서 종양 성장을 유의하게 억제하고 세포자멸사를 증가시킵니다. CAY10526은 BCL-2 및 BCL-XL(항-세포자멸사) 단백질 수준을 감소시키고 BAX 및 BAK(프로-세포자멸사) 및 절단된 카스파제 3 수준을 증가시킵니다. CAY10526은 mPGES1을 발현하는 3개의 흑색종 세포주에서 세포 생존력(IC50<5μM)을 억제합니다.

PGF1β is the C-9 epimer of PGF1α.

A stable analog of PGF 2α 2glyceryl ester

Prostaglandin D1(PGD1) alcohol is the synthetic analog of PGD1 with a primary alcohol in place of the C-1 carboxyl.

AF3485 is a selective 3-aminocarbazole inhibitor of mPGES-1, blocking the synthesis of PGE2 but not PGF2α in A549 cells stimulated with IL-1β (IC50s = 2.9 and >100 µM, respectively).

Prostaglandins have a short life in vivo because NAD+-dependent 15-hydroxy prostaglandin dehydrogenase (15-PGDH) catalyzes their oxidation to 15-keto metabolites with greatly reduced biological activity.

The actions of many clinical prostaglandins, including those used for estrous synchronization and for reduction of intraocular pressure, are mediated through the FP receptor.

Prostaglandin F2α alcohol (PGF2α-OH) is an analog of PGF2α in which the C-1 carboxyl group has been reduced to a primary alcohol.

Prostaglandin F1α (PGF1α) alcohol is an analog of PGF1α with a primary alcohol replacing the C-1 carboxyl group.

Prostaglandin D2 (PGD2) plays a pharmacological role in allergic and asthmatic anaphylaxis, normal physiological sleep and lowering of body temperature, as well as inhibits platelet aggregation and relaxes vascular smooth muscle.

Prostaglandin D1 (PGD1) is the theoretical D-series metabolite of DGLA, but to date it has not been isolated as a natural product.

13(R)-HODE is the opposite enantiomer of the 13(S)-HODE produced when linoleic acid is incubated with soybean lipoxygenase.

5(6)-DiHET is a fully racemic version of the enantiomeric forms biosynthesized from 5(6)-EET by epoxide hydrolases.

고독성 피부 자극제인 텔레오시딘 A1(Lyngbyatoxin A)은 단백질 키나제 C(PKC)의 강력한 활성제입니다. Teleocidin A1은 HeLa 암세포에 대한 항증식 활성을 나타냅니다(IC50=9.2nM).

Limaprost-d3 is intended for use as an internal standard for the quantification of limaprost by GC- or LC-MS.

5(6)-DiHET is a fully racemic version of the enantiomeric forms biosynthesized from 5(6)-EET by epoxide hydrolases.

Epoxide hydrolases convert the EETs into vicinal diols, with the concurrent loss of much of their biological activity.

11-deoxy PGF2α is a synthetic analog of PGF2α.

11-deoxy Prostaglandin F2β (11-deoxy PGF2β) is an analog of PGF2β.