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| Product | Description | |
|---|---|---|
| Deoxycorticosterone | Deoxycorticosterone is a steroid hormone produced by the adrenal gland that possesses mineralocorticoid activity and acts as an aldosterone precursor. Deoxycorticosterone is an agonist for O. mykiss mineralocorticoid receptor ( rtMR ) transcription with EC 50 of 0.16 nM [3]. Deoxycorticosterone could acts as an immune stimulator in fish [4]. Uses: Scientific research. Group: Natural products. CAS No. 64-85-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-113414. |  |
| 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. |  |
| 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 | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. |  |
| 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. | |
| 11-Deoxycorticosterone-2,3,4-13C3 solution | 100 ?g/mL in methanol, ?99 atom % 13C, ?98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| 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 |
| Tetrahydro 11-deoxycorticosterone | Tetrahydro 11-deoxycorticosterone. Group: Biochemicals. Alternative Names: (3a,5b)-3,21-Dihydroxypregnan-20-one; a,21-Dihydroxy-5b-pregnan-20-one; , 11-Deoxytetra hydrocorticosterone. Grades: Highly Purified. CAS No. 567-03-3. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C21H34O3. US Biological Life Sciences. | Worldwide |
| Tetrahydro 11-deoxycorticosterone | Tetrahydro 11-deoxycorticosterone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 5-BETA-PREGNAN-3-ALPHA, 21-DIOL-20-ONE;21-HYDROXYPREGNANOLONE;TETRAHYDROCORTEXONE;TETRAHYDRODEOXYCORTICOSTERONE;TETRAHYDRODESOXYCORTICOSTERONE;TETRAHYDRO DOC;TETRAHYDRO CMPD ''Q'';TETRAHYDRO SUBSTANCE 'Q'. Product Category: Steroidal Compounds. CAS No. 567-03-3. Molecular formula: C21H34O3. Mole weight: 334.49. Purity: 0.95. Product ID: ACM567033. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tetrahydrodeoxycorticosterone | Tetrahydrodeoxycorticosterone, an neurosteroid, is a potent positive allosteric modulator (PAM) of GABA A receptor. Tetrahydrodeoxycorticosterone has potent neuroinhibitory properties [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Tetrahydro-11-deoxycorticosterone. CAS No. 567-03-3. Pack Sizes: 1 mg; 5 mg. Product ID: HY-113346. | |
| 11-Deoxy-18-hydroxycorticosterone | 11-Deoxy-18-hydroxycorticosterone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 11-DEOXY-18-HYDROXYCORTICOSTERONE;18-HYDROXY-11-DEOXYCORTICOSTERONE;18-HYDROXYDEOXYCORTICOSTERONE;18-HYDROXY DOC;18,20-EPOXY-20,21-DIHYDROXY-4-PREGNEN-3-ONE;18,21-DIHYDROXY-4-PREGNENE-3,20-DIONE;4-PREGNENE-18,21-DIOL-3,20-DIONE;4-PREGNEN-18,21-DIOL-3,20-. Product Category: Steroidal Compounds. CAS No. 379-68-0. Molecular formula: C21H30O4. Mole weight: 346.46. Purity: 0.95. IUPACName: (8R,9S,10R,13R,14S,17S)-17-(2-hydroxyacetyl)-13-(hydroxymethyl)-10-methyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one. Canonical SMILES: CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4C(=O)CO)CO. Density: 1.22g/cm³. ECNumber: 206-834-3. Product ID: ACM379680. Alfa Chemistry ISO 9001:2015 Certified. | |
| 11-Deoxy corticosterone | 11-Deoxy corticosterone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Desoxycortone, Cortexone, Desossicortone, Desoxicortonum, Deoxycortone, desoxycorticosterone, 11-Deoxycorticosterone, 21-Hydroxyprogesterone, Deoxycorticosterone, Desoxycorticosteronum, 11-Desoxycorticosterone, Reichstein Q, Reichsteins substance Q, Kendalls desoxy compound B, 11-Dcortic, Desossicortone [DCIT], 11-Dehydroxycorticosterone, 4-Pregnen-21-ol-3,20-dione, Corticosterone, 11-deoxy-, Progesterone, 21-hydroxy-. Product Category: Steroidal Compounds. Appearance: white to creamy-white crystalline powder. CAS No. 64-85-7. Molecular formula: C21H30O3. Mole weight: 330.46. Purity: 0.95. IUPACName: (8S,9S,10R,13S,14S,17S)-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one. Canonical SMILES: CC12CCC3C(C1CCC2C(=O)CO)CCC4=CC(=O)CCC34C. Density: 1.15 g/cm³. ECNumber: 200-596-4. Product ID: ACM64857. Alfa Chemistry ISO 9001:2015 Certified. | |
| 11-Deoxy Corticosterone-d7 | Labelled Deoxycorticosterone. A mineralocorticoid that occurs in adrenal cortex. It acts as a precursor to Aldosterone (A514700). Group: Biochemicals. Alternative Names: 21-Hydroxypregn-4-ene-3,20-dione-d7; 11-Deoxycorticosterone-d7; 11-Dehydroxy-corticosterone-d7; 11-Desoxycorticosterone-d7; 21-Hydroxy-3,20-dioxopregn-4-ene-d7; 21-Hydroxy-4-pregnane-3,20-dione-d7. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 11-Deoxy Corticosterone-d8 | Labeled Deoxycorticosterone. A mineralocorticoid that occurs in adrenal cortex. It acts as a precursor to Aldosterone. Group: Biochemicals. Alternative Names: 21-Hydroxypregn-4-ene-3,20-dione-d8; 11-Deoxycorticosterone-d8; 11-Dehydroxy-corticosterone-d8; 11-Desoxycorticosterone-d8; 21-Hydroxy-3,20-dioxopregn-4-ene-d8; 21-Hydroxy-4-pregnane-3,20-dione-d8. Grades: Highly Purified. CAS No. 55487-63-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 11-Deoxy Corticosterone Pivalate | 11-Deoxycorticosterone Pivalate is a mineralocorticoid hormone and an analog of desoxycorticosterone. 11-Deoxycorticosterone Pivalate is used in the treatment of adrenocortical insufficiency. It is used to treat in patients suffering from rheumatoid arthritis. Group: Biochemicals. Alternative Names: 21-(2,2-dimethyl-1-oxopropoxy)pregn-4-ene-3,20-dione; 11-Deoxycorticosterone Pivalate; 21-Hydroxypregn-4-ene-3,20-dione pivalate; Cortexone M; DOCP; DTMA; Deoxycorticosterone Trimethylacetate; Deoxycortone Pivalate; Deoxycortone Trimethylacetate; Desoxycorticosterone Pivalate; Desoxycortisone pivalate; Desoxycortone pivalate; NSC 95278; Neodin-Depositum; Percorten M; Percorten Pivalate. Grades: Highly Purified. CAS No. 808-48-0. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| 21-(Cyclohex-1-enyl)pregn-4-ene-3,20-dione | 21-(Cyclohex-1-enyl)pregn-4-ene-3,20-dione, is a derivative of deoxycorticosterone (D232590), a mineralocorticoid that occurs naturally in the adrenal cortex. It acts as a precursor to Aldosterone (A514700). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 50mg. Molecular Formula: C27H38O2, Molecular Weight: 394.59. US Biological Life Sciences. | Worldwide |
| 21-Hydroxyprogesterone 21-hemisuccinate | 21-Hydroxyprogesterone 21-hemisuccinate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Deoxycorticosterone 21-hemisuccinate; 21-Hydroxypregn-4-ene-3,20-dione 21-(hydrogen succinate); 4-[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-oxoethoxy]-4-oxobutanoic acid; succinic acid mono-(3,20-dioxo-pregn-4-en-21-yl ester); 21-Hydroxyprogesterone 21-hemisuccinate; Bernsteinsaeure-mono-(3,20-dioxo-pregn-4-en-21-ylester); 4-Pregnen-21-ol-3,20-dione 21-hemisuccinate; 11-Deoxycorticosterone hydrogen succinate; Cortexone 21-hemisuccinate; 21-Hydroxy-4-pregnene-3,20-dione 21-hemisuccinate. Product Category: Steroidal Compounds. CAS No. 10215-74-4. Molecular formula: C25H34O6. Mole weight: 430.53. Purity: 0.95. IUPACName: 4-[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-oxoethoxy]-4-oxobutanoicacid. Canonical SMILES: CC12CCC3C(C1CCC2C(=O)COC(=O)CCC(=O)O)CCC4=CC(=O)CCC34C. Density: 1.22g/cm³. ECNumber: 233-528-7. Product ID: ACM10215744. Alfa Chemistry ISO 9001:2015 Certified. | |
| 5 α -Di hydrodeoxycorticost erone | 5 α -Di hydrodeoxycorticost erone. Group: Biochemicals. Alternative Names: 21-Hydroxy-5α-pregnane-3,20-dione; 5α-Dihydro-11-deoxycorticosterone; 5α-Pregnan-21-ol-3,20-dione; Allopregnane-21-ol-3,20-dione. Grades: Highly Purified. CAS No. 298-36-2. Pack Sizes: 50mg. Molecular Formula: C21H32O3, Molecular Weight: 332.48. 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. | |
| Metyrapol | Metyrapol, a dipyridine derivative, has been found to be a 11-deoxycorticosterone hydroxylation inhibitor and could always used as a medical diagnostic reagent in detection of liver diseases. Synonyms: SU-5236; SU5236; SU 5236; Metyrapol; 2-Methyl-1,2-bis(3-pyridyl)-1-propanol; SU-5236; 2-methyl-1,2-dipyridin-3-ylpropan-1-ol. Grades: 98%. CAS No. 17159-42-1. Molecular formula: C14H16N2O. Mole weight: 228.29. | |
| steroid 21-monooxygenase | A P-450 heme-thiolate protein responsible for the conversion of progesterone and 17α-hydroxyprogesterone to their respective 21-hydroxylated derivatives, 11-deoxycorticosterone and 11-deoxycortisol. Involved in the biosynthesis of the hormones aldosterone and cortisol. The electron donor is EC 1.6.2.4, NADPH-hemoprotein reductase. Group: Enzymes. Synonyms: steroid 21-hydroxylase; 21-hydroxylase; P450c21; CYP21A2 (gene name). Enzyme Commission Number: EC 1.14.14.16. CAS No. 9029-68-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0913; steroid 21-monooxygenase; EC 1.14.14.16; 9029-68-9; steroid 21-hydroxylase; 21-hydroxylase; P450c21; CYP21A2 (gene name). Cat No: EXWM-0913. |  |
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