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Pregnenolone derivative, a steroid hormone involved in the steroidogenesis of progesterone, mineralocorticoids, glucocorticoids, androgens, and estrogens. Group: Biochemicals. Alternative Names: (3 β)-3-(Acetyloxy)-pregn-5-en-20-one; 3 β-Acetoxy-5-pregnen-20-one; 3 β-Acetoxy-Δ5-pregnen-20-one; 3 β-Hydroxypregn-5-en-20-one Acetate; 3 β-Pregn-5-enol-20-one Acetate; 5-Pregnen-3 β-ol-20-one Acetate; 5-Pregnene-3 β-acetoxy-20-one; Antofin; Artivis; Enescorb; NSC 64827; Pregenolone Acetate; PregnenoloneAcetate; Pregnenolone-3-acetate; Previsone; Sharmone. Grades: Highly Purified. CAS No. 1778-02-5. Pack Sizes: 25mg. US Biological Life Sciences.
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16-Dehydro PregnenoloneAcetate
16-DehydropregnenoloneAcetate is the dehydration product of PregnenoloneAcetate. 16-DehydropregnenoloneAcetate is used in the preparation of pregnane derivatives and its glycosides as potential anticancer agents. Group: Biochemicals. Alternative Names: (3 β)-3-(Acetyloxy)pregna-5,16-dien-20-one; 3 β-Hydroxypregna-5,16-dien-20-one Acetate; (-)-16-DehydropregnenoloneAcetate; 16,17-DidehydropregnenoloneAcetate; 16-DPA; 16-Dehydropregnenolone-3 β-acetate; 20-Oxopregna-5,16-dien-3 β-yl Acetate; 3 β-Acetoxypregna-5,16-dien-20-one; 3 β-Acetyloxy-pregna-5,16-dien-20-one; NSC 37741; Pregnadienolone Acetate. Grades: Highly Purified. CAS No. 979-02-2. Pack Sizes: 10g. US Biological Life Sciences.
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Abiraterone Related Compound 1 (Pregnenolone-16-ene Acetate)
Cas No. 979-02-2.
Abiraterone Related Compound 3 (Pregnenolone-16-ene Acetate Oxime)
Pregnenolone-16-ene Acetate Oxime is used in the synthesis of pegnange derivatives as antioxidant and anti-dyslipidemic agents. Synonyms: Abiraterone Impurity 3,Pregnenolone-16-ene Acetate Oxime. Grades: > 95%. CAS No. 2174-13-2. Molecular formula: C23H33NO3. Mole weight: 371.52.
17-MethyI-18-norandrosta-5,13(17)-dien-3 β-ol 3-Acetate s an impurity of Pregnenolone (P712200) which is a steroid hormone involved in the steroidogenesis of progesterone, mineralocorticoids, glucocorticoids, androgens, and estrogens. As such it is a prohormone. Pregnenolone is a GABAA antagonist and increases neurogenesis in the hippocampus. It is a modulator of cytochrome P 450-3A. Group: Biochemicals. Grades: Highly Purified. CAS No. 23930-63-4. Pack Sizes: 2.5mg, 25mg. Molecular Formula: C21H30O2. US Biological Life Sciences.
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Allopregnandiol 20-(Hydrogen Sulfate) Sodium Salt
(3 β,5α,20R)-Pregnane-3,20-diol, 20-Sulfate Sodium Salt is sulfate conjugated metabolite of Allopregnandiol (CAS#516-33-0). (3 β,5α,20R)-Pregnane-3,20-diol, 20-Sulfate Sodium Salt can be obtained from 5α-Pregnan-3 β-ol-20-one 3 β-Acetate (P711315) which is a derivative of Pregnenolone (P712200); a steroid hormone involved in the steroidogenesis of progesterone, mineralocorticoids, glucocorticoids, androgens, and estrogens. As such it is a prohormone. Pregnenolone is a GABAA antagonist and increases neurogenesis in the hippocampus. It is a modulator of cytochrome P 450-3A. Group: Biochemicals. Grades: Highly Purified. CAS No. 215855-82-6. Pack Sizes: 1mg, 10mg. Molecular Formula: C21H35NaO5S, Molecular Weight: 422.55. US Biological Life Sciences.
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Allopregnandiol 3-(Hydrogen Sulfate) Sodium Salt
Allopregnandiol 3-(Hydrogen Sulfate) Sodium Salt is sulfate conjugated metabolite of Allopregnandiol (CAS#516-33-0). (3 β,5α,20R)-Pregnane-3,20-diol, 20-Sulfate Sodium Salt can be obtained from 5α-Pregnan-3 β-ol-20-one 3 β-Acetate (P711315) which is a derivative of Pregnenolone (P712200); a steroid hormone involved in the steroidogenesis of progesterone, mineralocorticoids, glucocorticoids, androgens, and estrogens. As such it is a prohormone. Pregnenolone is a GABAA antagonist and increases neurogenesis in the hippocampus. It is a modulator of cytochrome P 450-3A. Group: Biochemicals. Grades: Highly Purified. CAS No. 215855-85-9. Pack Sizes: 1mg, 5mg. Molecular Formula: C21H35NaO5S, Molecular Weight: 422.55. US Biological Life Sciences.
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17α-hydroxyprogesterone deacetylase
A microsomal cytochrome P-450 (heme-thiolate) protein that catalyses two independent reactions at the same active site - the 17-hydroxylation of pregnenolone and progesterone, which is part of glucocorticoid hormones biosynthesis (EC 1.14.14.19), and the conversion of the 17-hydroxylated products via a 17,20-lyase reaction to form androstenedione and 3β-hydroxyandrost-5-en-17-one, leading to sex hormone biosynthesis. The activity of this reaction is dependent on the allosteric interaction of the enzyme with cytochrome b5 without any transfer of electrons from the cytochrome. The enzymes from different organisms differ in their substrate specificity. While the enzyme...son do not accept the former, and the enzyme from guinea pig does not accept the latter. Group: Enzymes. Synonyms: C-17/C-20 lyase; 17α-hydroxyprogesterone acetaldehyde-lyase; CYP17; CYP17A1 (gene name); 17α-hydroxyprogesterone 17,20-lyase. Enzyme Commission Number: EC 1.14.14.32. CAS No. 62213-24-5. 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-0930; 17α-hydroxyprogesterone deacetylase; EC 1.14.14.32; 62213-24-5; C-17/C-20 lyase; 17α-hydroxyprogesterone acetaldehyde-lyase; CYP17; CYP17A1 (gene name); 17α-hydroxyprogesterone 17,20-lyase. Cat No: EXWM-0930.
7-Bromo-3-O-acetyl Pregnenolone
DHEA (De hydroepiandrosterone) derivative, useful due to their cosmetic use. Group: Biochemicals. Alternative Names: (3 β)-3-(Acetyloxy)-7-bromo-pregn-5-en-20-one; 7-Bromo-3 β-hydroxy-pregn-5-en-20-one Acetate. Grades: Highly Purified. CAS No. 114417-65-1. Pack Sizes: 10mg. US Biological Life Sciences.
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Pregnenolone 16-acetonitrile
Heterocyclic Organic Compound. CAS No. 102812-95-3. Catalog: ACM102812953.
Pregnenolone Carbonitrile
Pregnenolone carbonitrile (PCN) is a derivative of pregnenolone and acts as an agonist of the rodent pregnane X receptor (PXR). Synonyms: PCN; Pregnenolone 16α-carbonitrile; SC-4674; (3S,8S,9S,10R,13S,14S,16R,17S)-17-acetyl-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-16-carbonitrile. Grades: ≥98%. CAS No. 1434-54-4. Molecular formula: C22H31NO2. Mole weight: 341.5.
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