Lipids and Lipid Derivatives
eMolecules 142878-12-4 | Medchem Express | U-73343 | 5mg | 482203907 | HY-108630 | 466.666 | C29H42N2O3
Ambeed | 57-Dimethyl-N-(trans-4-(pentyloxy)cyclohexyl)pyrazolo[15-a]pyrimidine-3-carboxamide | 1mg | 534567031 | A181720 | 1919820-28-2 | 358.486 | C20H30N4O2
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Selleck Chemical LLC Estradiol Benzoate S4110-10mM/1mL
Estradiol benzoate( -Estradiol 3-benzoate) is an estradiol analog which binds to the human murine and chicken ER with IC50 of 22-28 nM
Sigma Aldrich Fine Chemicals Biosciences beta-Estradiol 3-benzoate >=97% | 50-50-0 | MFCD00003692 | 5G
beta-Estradiol 3-benzoate >=97% | Purity: >=97% | Mol Wt: 376.49 | 50-50-0 | MFCD00003692 | 5G
Medchemexpress LLC Bazedoxifene (acetate)-D | 198481-33-3 | MFCD09260074 | C32H38N2O5 | 100 MG
Bazedoxifene (acetate)-D is a solid compound with a molecular formula of C32H38N2O5 and a molecular weight of 530.65. It is classified as a selective estrogen receptor modulator and a bone density conservation agent. This compound helps to inhibit bone resorption and favor bone mineralization, making it suitable for addressing conditions like osteoporosis and promoting bone fracture healing. It is an FDA-approved, prescription-only drug administered orally.
- Functions as a selective estrogen receptor modulator
- Acts as a bone density conservation agent
- Inhibits bone resorption
- Promotes bone mineralization and regeneration
- Utilized in treating osteoporosis and healing bone fractures
- FDA-approved, available by prescription only
- Administered via oral route
Medchemexpress LLC Norethisterone enanthate | 3836-23-5 | 99.5% | C27H38O3 | 1 ML
Norethisterone enanthate is a long-acting parenteral progestogen used as an intramuscular contraceptive agent. It is also an orally active click chemistry reagent containing an alkyne group, enabling copper-catalyzed azide-alkyne cycloaddition with azide-containing molecules.
- Long-acting parenteral progestogen
- Functions as an intramuscular contraceptive agent
- Orally active
- Contains an alkyne group for click chemistry applications
- Powder stable at -20°C for 3 years or 4°C for 2 years
- Solution stable at -80°C for 2 years or -20°C for 1 year
- Store stock solutions aliquoted to prevent inactivation from repeated freeze-thaw cycles
Medchemexpress LLC 19-Norpregn-4-en-20-yn-3-one, 17-[(1-oxoheptyl)oxy]-, (17α)- | 3836-23-5 | 99.5% | C27H38O3 | 500 MG
Norethisterone enanthate is a long-acting parenteral progestogen. It is orally active and functions as a click chemistry reagent, containing an Alkyne group that can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules possessing Azide groups. This product is for research use only and not sold to patients.
- Long-acting parenteral progestogen
- Orally active
- Functions as a click chemistry reagent
- Contains an alkyne group for copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Can be used as an intramuscular contraceptive agent (in vitro)
- Inhibits fertility in female rats (in vivo)
Medchemexpress LLC Medroxyprogesterone acetate-d3 | 71-58-9 | >98.1% | 5 MG
Medroxyprogesterone acetate-d3 is a deuterium-labeled form of Medroxyprogesterone acetate. This synthetic steroid interacts with progesterone, androgen, and glucocorticoid receptors.
- Used as a tracer
- Functions as an internal standard for quantitative analysis
- Applicable in NMR, GC-MS, or LC-MS
Medchemexpress LLC Bazedoxifene (acetate) | 198481-33-3 | 99.9% | C32H38N2O5 | 50 MG
Bazedoxifene (acetate) is an oral, nonsteroidal selective estrogen receptor modulator (SERM) primarily used in research for osteoporosis and pancreatic cancer. It acts as an inhibitor of IL-6/GP130 protein-protein interactions and shows IC50s of 23 nM and 99 nM for ERα and ERβ respectively. This product is intended for laboratory chemical applications and research use only.
- Oral, nonsteroidal selective estrogen receptor modulator
- Inhibitor of IL-6/GP130 protein-protein interactions
- Suitable for osteoporosis research
- Suitable for pancreatic cancer research
- Available as a white to off-white solid
- Purity of 99.9%
Medchemexpress LLC Glepaglutide acetate | 99.5% | 4376.06 | 5 MG
Glepaglutide acetate is a long-acting GLP-2 analogue and a potent GLP-2R agonist. It functions by reducing faecal output and increasing intestinal absorption. This compound also helps in alleviating small intestinal inflammation, making it suitable for research applications in inflammatory bowel disease (IBD) and Crohn's disease.
- Long-acting GLP-2 analogue
- Potent GLP-2R agonist
- Reduces faecal output
- Increases intestinal absorption
- Alleviates small intestinal inflammation
- Suitable for inflammatory bowel disease (IBD) research
- Suitable for Crohn's disease research
Medchemexpress LLC Petrelintide acetate | 99.8% | 4191.69 | 10 MG
Petrelintide (ZP8396) acetate is a dual amylin and calcitonin receptor agonist (DACRA). It causes a selective reduction in high-fat diet intake in diet-induced obese (DIO) rats, leading to a loss of fat mass and preservation of lean mass during weight reduction. Petrelintide acetate can be used in diabetes research.
- Dual amylin and calcitonin receptor agonist (DACRA).
- Elicits a selective reduction in high-fat diet intake in DIO rats.
- Accompanied by a loss of fat mass and preservation of lean mass during weight reduction.
- Can be utilized in diabetes research.
Sigma Aldrich Fine Chemicals Biosciences Norethisterone acetate European Pharmacopoeia (EP) Reference Standard | 51-98-9 | MFCD00271615 |
Norethisterone acetate European Pharmacopoeia (EP) Reference Standard | Mol Wt: 340.46 | 51-98-9 | MFCD00271615 |
Medchemexpress LLC Fluorogestone acetate | 2529-45-5 | MFCD00243094 | 99.6% | 406.49 g/mol | C23H31FO5 | 25MG
Fluorogestone acetate is a synthetic progesterone derivative used to inhibit ovulation and synchronize the estrous cycle in cattle. It is intended for research and veterinary applications and is characterized by defined purity and chemical properties.
- Purity: 99.6%.
- Molecular formula: C23H31FO5.
- Molecular weight: 406.49 g/mol.
- Application: inhibits ovulation and synchronizes estrous cycles in cattle.
- Packaging: available in multiple small pack sizes for dosing flexibility.
- Intended use: for research use and veterinary studies, not for human therapeutic use.
Medchemexpress LLC Medroxyprogesterone | 520-85-4 | 98.8% | 1 G
Medroxyprogesterone (17α-Hydroxy-6α-methylprogesterone) is a synthetic human variant of progesterone that acts as a progesterone receptor agonist with oral activity. It can induce cell proliferation through the PI3K/Akt signaling pathway and has an inhibitory effect on atherosclerosis in mice.
- Progesterone receptor agonist with oral activity.
- Induces cell proliferation via PI3K/Akt signaling pathway.
- Inhibitory effect on atherosclerosis in mice.
- Less effective progesterone agonist activity than Medroxyprogesterone acetate.
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