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| Product | Description | |
|---|---|---|
| Deoxycorticosterone acetate | Deoxycorticosterone acetate (DOCA) is an adrenocortin, acts as a precursor to aldosterone. Deoxycorticosterone acetate is a mineralocorticoid receptor agonist. Deoxycorticosterone acetate can cause severe renal injury, including inflammation, fibrosis, glomerular damage, and proteinuria [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: 11-Deoxycorticosterone acetate; DOC acetate; Cortexone acetate. CAS No. 56-47-3. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1472. |  |
| Deoxycorticosterone acetate | Deoxycorticosterone acetate is a steroid hormone used for intramuscular injection for replacement therapy of the adrenocortical steroid. Synonyms: Deoxycorticosterone Acetate; DOCA; Percotol; Cortexone acetate. Grades: >98%. CAS No. 56-47-3. Molecular formula: C23H32O4. Mole weight: 372.5. |  |
| Deoxycorticosterone Acetate | Deoxycorticosterone Acetate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: [2-[(8S,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate. Product Category: Steroidal Compounds. Appearance: White solid. CAS No. 56-47-3. Molecular formula: C23H32O4. Mole weight: 372.5. Purity: 0.95. IUPACName: [2-[(8S,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl]acetate. Canonical SMILES: CC(=O)OCC(=O)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C. Density: 1.14 g/cm³. ECNumber: 200-275-9. Product ID: ACM56473. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 17α-Hydroxy-11-deoxycorticosterone-21-acetate | 17α-Hydroxy-11-deoxycorticosterone-21-acetate is an acetate substance 'S' - a synthetic steroid as carbaryl synergist. Synonyms: 21-(Acetyloxy)-17-hydroxypregn-4-ene-3,20-dione; 11-Deoxycortisol 21-acetate; 17-Hydroxy-21-acetoxyprogesterone; 21-Acetoxy-17α-hydroxyprogesterone; Cortexolone 21-acetate; Reichstein substance S 21-acetate. Grades: > 95%. CAS No. 640-87-9. Molecular formula: C23H32O5. Mole weight: 388.5. | |
| 17α-Hydroxy-11-deoxycorticosterone-21-acetate | An acetate substance 'S' - a synthetic steroid as carbaryl synergist. Group: Biochemicals. Alternative Names: 21-(Acetyloxy)-17-hydroxypregn-4-ene-3,20-dione. Grades: Highly Purified. CAS No. 640-87-9. Pack Sizes: 50mg. US Biological Life Sciences. |  Worldwide |
| (3α,5 β)-Tetrahydro 11-Deoxycorticosterone 21-Acetate | Tetrahydro 11-Deoxycorticosterone (T293270) derivative. Used in the preparation of steroids with the ability to potentiate GABA-receptor-mediated Cl- uptake into cerebral cortical synaptoneurosomes. Group: Biochemicals. Alternative Names: 5 β-Pregnan-20-one-3α,21-diol-21-acetate; 5 β-Pregnan-3α,21-diol-20-on-21-acetate. Grades: Highly Purified. CAS No. 2402-24-6. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| (3 β,5 β)-Tetrahydro 11-Deoxycorticosterone 21-Acetate | (3 β,5 β)-Tetrahydro 11-Deoxycorticosterone 21-Acetate displays efficient blocking activity towards 3α-hydroxypregnane-steroid action but minimal activity against GABA. Group: Biochemicals. Alternative Names: 21-Acetoxy-3 β-hydroxy-5 β-pregnan-20-one; 3 β,21-Dihydroxy-5 β-pregnan-20-one 21-Acetate. Grades: Highly Purified. CAS No. 10147-45-2. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| BMS 182874 | BMS 182874 is an orallyactive, highly selective endothelin receptor ( ET A receptor) antagonist, with IC 50 value of 0.150 μM, K i of 0.055 μM. BMS 182874 reduces the arterial pressure of Deoxycorticosterone acetate (HY-B1472) induced hypertension model in rats, and can be used for cardiovascular disease research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 153042-42-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-118497. | |
| Deoxy Corticosterone Acetate | Adrenocortical / mineralocorticoid Steroid. Group: Biochemicals. Alternative Names: 21-(Acetyloxy)-pregn-4-ene-3,20-dione; 11-Deoxycorticosterone 21-Acetate; 21-Acetoxy-3,20-diketopregn-4-ene; 21-Acetoxypregn-4-en-3,20-dione; 21-Hydroxypregn-4-ene-3,20-dione Acetate; Arcort; Bio-Corten; Cortacet; Cortate; Cortenil; Cortesan; Cortexone acetate; Cortifar; Cortigen; Cortinaq; Cortiron; Cortivis; Cortixyl; DCA; DOC acetate; DOCA; Decorten; Decortin; Decosteron; Decosterone; Decostrate. Grades: Highly Purified. CAS No. 56-47-3. Pack Sizes: 1g, 5g, 10g. Molecular Formula: C??H??O?, Molecular Weight: 372.5. US Biological Life Sciences. | Worldwide |
| LY-272015 hydrochloride | LY-272015 hydrochloride is an orally active, specific 5-HT 2B receptor antagonist. LY-272015 hydrochloride completely inhibits the phosphorylation of ERK2 induced by 5-HT or BW723C86. LY-272015 hydrochloride is antihypertensive in Deoxycorticosterone Acetate (DOCA)-salt-hypertensive rats [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 172895-15-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100851A. | |
| Deoxycorticosterone 21-Glucoside | Deoxycorticosterone 21-Glucoside. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Percorten, Desoxycorton glucosid, Desoxycortone 21-D-glucoside, EINECS 224-349-5, CID107540, Pregn-4-ene-3,20-dione, 21-(beta-D-glucopyranosyloxy)-, 4319-56-6. Product Category: Steroidal Compounds. CAS No. 4319-56-6. Molecular formula: C27H40O7. Mole weight: 476.6. Purity: 0.95. IUPACName: (8S,9S,10R,13S,14S)-10,13-dimethyl-17-[2-(1,2,3,6-tetrahydroxy-4-oxohexoxy)acetyl]-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one. Canonical SMILES: C[C@H]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2C(=O)CO[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)C. Density: 1.32g/cm³. Product ID: ACM4319566. Alfa Chemistry ISO 9001:2015 Certified. | |
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