Lipids and Lipid Derivatives
Medchemexpress LLC Medroxyprogesterone | 520-85-4 | 99.3% | 50 MG
Medroxyprogesterone (Standard) is the analytical standard of Medroxyprogesterone, intended for research and analytical applications. This product is for research use only and not sold to patients.
- Used as an analytical standard
- Suitable for qualitative, quantitative, and methodological research experiments
- Applicable in techniques such as HPLC, GC, and MS
Apexbio Technology LLC Medroxyprogesterone acetate 71-58-9 10mM (in 1mL DMSO)
Medroxyprogesterone acetate (MPA) is a synthetic steroidal derivative structurally related to the endogenous hormone progesterone classified as a progestin Acting primarily through binding to progesterone receptors it modulates gene transcription influencing endometrial proliferation and reproductive pathways Additionally MPA exhibits affinity toward glucocorticoid receptors which may contribute to its physiological effects In biomedical research MPA serves as a standard experimental tool to investigate progesterone receptor signaling mechanisms and steroid hormone interactions Furthermore it is widely used in studies focused on reproductive biology contraceptive mechanisms hormone replacement therapy models oncology research involving hormone-responsive tumors and conditions such as endometriosis
Apexbio Technology LLC Deoxycorticosterone acetate 56-47-3 50mg
Deoxycorticosterone acetate (56-47-3) is a small-molecule agonist targeting mineralocorticoid receptors (MR) It is designed to activate MR thereby regulating renal sodium reabsorption and potassium excretion Deoxycorticosterone acetate exerts its biological activity primarily through interaction with cytoplasmic mineralocorticoid receptors leading to nuclear translocation and modulation of electrolyte balance Typical IC50 values associated with its mineralocorticoid receptor binding affinity have been reported in the nanomolar range Based on these pharmacological properties Deoxycorticosterone acetate holds research potential in studies of electrolyte balance adrenal insufficiency modeling and the pathophysiology of hypertension as well as models investigating mineralocorticoid receptor-dependent signaling and renal or cardiovascular physiology
Apexbio Technology LLC Medroxyprogesterone 520-85-4 50mg
Medroxyprogesterone (CAS 520-85-4) is a small-molecule agonist targeting the progesterone receptor It is designed to activate progesterone receptor-mediated intracellular signaling pathways thereby regulating cellular proliferation Medroxyprogesterone exerts its biological activity primarily through agonism of the progesterone receptor modulating pathways such as PI3K/Akt signaling In preclinical mouse models medroxyprogesterone demonstrates inhibitory activity on atherosclerotic lesion formation Based on these pharmacological properties medroxyprogesterone holds research potential in the study of progesterone receptor-mediated biological processes cellular proliferation and vascular pathology
Medchemexpress LLC Bazedoxifene (acetate)-D | 198481-33-3 | 99.9% | C32H38N2O5 | 50 MG
Bazedoxifene (acetate)-D is the D-crystal form compound of Bazedoxifene acetate, an orally active, nonsteroidal selective estrogen receptor modulator (SERM) with IC50s of 23 nM for ERα and 99 nM for ERβ.
- D-crystal form compound
- Orally active, nonsteroidal selective estrogen receptor modulator (SERM)
- IC50s of 23 nM for ERα and 99 nM for ERβ
- Purity of 99.9%
- Molecular weight of 530.65
- Chemical formula: C32H38N2O5
- CAS number: 198481-33-3
- Appears as a solid
- Color is white to off-white
- Soluble in DMSO at 50 mg/mL
Medchemexpress LLC Fluorogestone acetate | 2529-45-5 | MFCD00243094 | 99.6% | 406.49 | C23H31FO5 | 100MG
Fluorogestone acetate is a synthetic progesterone analog used to inhibit ovulation and synchronize the estrous cycle in cattle by suppressing luteinizing hormone (LH) release. It is supplied as a high-purity reagent in weighed milligram quantities for research and veterinary reproductive management applications.
- Inhibits ovulation and synchronizes the estrous cycle in cattle.
- Acts by suppressing luteinizing hormone (LH) release.
- High purity: 99.6%.
- Molecular formula: C23H31FO5; molecular weight: 406.49.
- Available in multiple package sizes, including 100 mg.
- Provided in weighed quantities suitable for formulation and analytical use.
Medchemexpress LLC Oxyphenisatin acetate | 115-33-3 | MFCD00022793 | 98.0% | 401.41 | C24H19NO5 | 50 MG
Oxyphenisatin acetate is the acetylated prodrug of oxyphenisatin, historically used as a laxative. This listing describes a research-grade chemical supplied for analytical and laboratory studies; it is intended for research use only and not for human or veterinary use.
- Acetylated prodrug of oxyphenisatin.
- Used in biochemical and autophagy-related research.
- CAS number: 115-33-3.
- Molecular formula C24H19NO5 and molecular weight ~401.41.
- Typically supplied as a solid with high purity (commonly ≥98%).
Sigma Aldrich Fine Chemicals Biosciences Progesterone United States Pharmacopeia (USP) Reference Standard | 57-83-0 | MFCD00003658 | 200MG
Progesterone United States Pharmacopeia (USP) Reference Standard | Mol Wt: 314.46 | 57-83-0 | MFCD00003658 | 200MG
Medchemexpress LLC Levonorgestrel | 797-63-7 | 100.0% | 100 MG
Levonorgestrel is an orally active inhibitor of progesterone. It has anticancer activity and can induce apoptosis. It can be used as a contraceptive and in combination with other medications. Levonorgestrel can also be used in the study of osteoporosis and uterine leiomyoma.
- Orally active inhibitor of progesterone.
- Exhibits anticancer activity.
- Induces apoptosis.
- Used as a contraceptive.
- Can be used in combination with other medications.
- Applicable in the study of osteoporosis and uterine leiomyoma.
Sigma Aldrich Fine Chemicals Biosciences Deoxycorticosterone acetate | 56-47-3 | MFCD00003660 | 1G
Deoxycorticosterone acetate | Purity: >=98% (HPLC) | Mol Wt: 372.5 | 56-47-3 | MFCD00003660 | 1G
Sigma Aldrich Fine Chemicals Biosciences U 18666A powder | 3039-71-2 | MFCD00210908 | 25MG
U 18666A powder | Purity: >=98% (HPLC) | Mol Wt: 424.06 | 3039-71-2 | MFCD00210908 | 25MG
Medchemexpress LLC UCL-TRO-1938 5MG
UCL-TRO-1938 is a potent allosteric activator of PI3Kα with an EC50 value of approximately 60 μM. UCL-TRO-1938 can induce cell proliferation and has cardioprotective and neural regeneration effects.