Lipids and Lipid Derivatives
Medchemexpress LLC Levonorgestrel | 797-63-7 | 99.98% | 500 MG
Levonorgestrel is an orally active inhibitor of progesterone. It exhibits anticancer activity and can induce apoptosis. This compound serves as a contraceptive and can be utilized in combination with other medications. Additionally, Levonorgestrel is employed in the study of osteoporosis and uterine leiomyoma.
- Inhibits cell proliferation and promotes apoptosis in uterine leiomyoma cells.
- Can inhibit progesterone production in luteal cells at high doses.
- Inhibits bone resorption, decreases bone turnover, and increases bone mineral content in Sprague-Dawley rats.
- Provides effective contraception in Apodemus agrarius mice when combined with quinestrol.
![Medchemexpress LLC Benzenesulfonamide, N-[(1R,2R)-2-[4-(2-methoxyphenyl)-1-piperazinyl]cyclohexyl]-, rel- | 2108567-79-7 | MFCD32690912 | 98.9% | C23H31N3O3S | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000261089.png-250.jpg)
Medchemexpress LLC Benzenesulfonamide, N-[(1R,2R)-2-[4-(2-methoxyphenyl)-1-piperazinyl]cyclohexyl]-, rel- | 2108567-79-7 | MFCD32690912 | 98.9% | C23H31N3O3S | 10MG
(rel)-ML-SI3 is a small-molecule modulator of TRPML (mucolipin) ion channels used to probe TRPML1/2/3 function and autophagy in biochemical and cell-based research. It inhibits TRPML1 and TRPML3 while activating TRPML2, and is supplied at high purity for experimental use.
- Modulates TRPML1, TRPML2, and TRPML3 activity in vitro.
- Inhibits TRPML1 with IC50 ≈ 3.1 μM.
- Activates TRPML2 with EC50 ≈ 3.3 μM.
- Inhibits TRPML3 with IC50 ≈ 28.5 μM.
- High purity suitable for biochemical and cellular assays.
- Available as powder and as DMSO solution for screening.
Cambridge Isotope Laboratories 17A-HYDROXYPROGESTERONE (2,3,4-13C3,98%), 5 MG, 1356154-92-1
17A-HYDROXYPROGESTERONE (2,3,4-13C3,98%), 5 MG, 1356154-92-1
Apexbio Technology LLC 17-Hydroxyprogesterone 68-96-2 50mg
17-Hydroxyprogesterone (68-96-2) is a small-molecule agonist targeting the progesterone receptor (PR) with partial agonist activity at glucocorticoid receptors (GR) and antagonist effects at mineralocorticoid receptors (MR) It modulates steroid hormone signaling pathways thereby influencing vascular tone and inflammation 17-Hydroxyprogesterone exerts its biological activity primarily through activation and modulation of steroid hormone receptors In animal models administration of 17-Hydroxyprogesterone demonstrates the ability to modulate vascular inflammation and uterine vascular tone Based on these pharmacological properties 17-Hydroxyprogesterone holds research potential in the screening of congenital adrenal hyperplasia and related metabolic syndromes as well as associations with respiratory distress syndrome and premature birth outcomes
TARGETMOL CHEMICALS INC 7alpha-Hydroxy-4-cholesten
Also available in 5 mg, 10 mg, 25 mg, 50 mg and bulk. Please contact Fisher for quotes. 7alpha-Hydroxy-4-cholesten-3-one is an intermediate in bile acid synthesis from cholesterol, a PXR agonist, and a biomarker for bile acid loss and diseases related to defective bile acid biosynthesis. It is also the physiological substrate for [CYP8B1]. Purity 99.14%
Cayman Chemical ResIbufogenIn 1mg
A cardiac glycoside that inhibits the Na+/K+-ATPase; exhibits cardiotonic, vasopressor, and respiratory stimulating actions in both animal and clinical models
[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)OC(=O)NCCC[N+](C)(C)CCO | 5mg | 779524216](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502467827.JPG-250.jpg)
eMolecules 794494-38-5 | DMHAPC-Chol | Broadpharm559.899 | C35H63N2O3 | 0.000 | CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)OC(=O)NCCC[N+](C)(C)CCO | 5mg | 779524216
DMHAPC-Chol | Broadpharm | 794494-38-5559.899 | C35H63N2O3 | 0.000 | CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)OC(=O)NCCC[N+](C)(C)CCO | 5mg | 779524216
eMolecules 72203-93-1 | Medchem Express | Calcitetrol | 1mg | 446265039 | HY-15157 | MFCD22124496 | 432.645 | C27H44O4
Medchem Express | Calcitetrol | 1mg | 446265039 | HY-15157 | 72203-93-1 | MFCD22124496 | 432.645 | C27H44O4
Medchemexpress LLC N-Caproicacid-d3 so 10mg
N-caproicacidsodiumsalt-d3 is the deuterium labeled N-caproicacidsodiumsalt[1]
Medchemexpress LLC 5,6-trans-Vitamin D2 | 51744-66-2 | 97.0% | C28H44O | 100 MG
5,6-trans-Vitamin D2 is an isomer of Vitamin D2. It is supplied as an off-white to light yellow solid with a molecular weight of 396.65. This product is for research use only and not intended for patient use.
- Isomer of vitamin D2
- For research use only
- Molecular weight of 396.65
- Appears as an off-white to light yellow solid
- Soluble in DMSO (25 mg/mL)
- In vivo dissolution protocols available
Medchemexpress LLC Vitamin D3 | 67-97-0 | C27H44O | 100 MG
Vitamin D3 (Cholecalciferol; Colecalciferol) is a naturally occurring form of vitamin D. It induces cell differentiation and prevents the proliferation of cancer cells. This product is an analytical standard and is intended for research and analytical applications.
- Used as a reference standard in assays.
- Utilized in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.
- Induces cell differentiation.
- Prevents proliferation of cancer cells.
Medchemexpress LLC 3-pyridin-3-ylpropyl (2S)-1-(3,3-dimethyl-2-oxopentanoyl)pyrrolidine-2-carboxylate | 186452-09-5 | MFCD00953146 | 99.8% | 360.45 g/mol | C20H28N2O4 | 10MG
GPI-1046 is a non-immunosuppressive immunophilin ligand used in research for its neuroprotective effects. It has been reported to upregulate glutamate transporter 1 (GLT1), reduce ethanol intake, and attenuate HIV-associated sensory neuropathy by modulating store-operated calcium entry. The compound is provided as a high-purity liquid (formula C20H28N2O4, MW ~360.45 g/mol).
- Non-immunosuppressive immunophilin ligand
- Reported neuroprotective activity
- Upregulates glutamate transporter 1 (GLT1)
- Attenuates HIV-associated sensory neuropathy via store-operated calcium entry modulation
- High purity (≈99.8%)
- Liquid appearance: colorless to light yellow
- Chemical formula C20H28N2O4; molecular weight ~360.45 g/mol
- Storage: 4°C, protect from light; in solvent: -80°C (6 months), -20°C (1 month)
Cambridge Isotope Laboratories 24R,25-DIHYDROXYVITAMIN D2 UNLABELED, 1 MG
24R,25-DIHYDROXYVITAMIN D2 UNLABELED, 1 MG