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17-Alpha Hydroxyprogesterone CAS:68-96-2

17 Alpha Hydroxyprogesterone
Nomen chemicum: 17-alpha-hydroxypregn-4-ene-3,20-dione
Formulae hypotheticae: C21H30O3
M. pondus: 330.47
CAS NO.: 68-96-2
Aspectus: White or almost white crystalline powder
Assay: ≥99.0%
Melting point: ≥214°C

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17-Hydroxyprogesterone (17-OHP) is an endogenous progestogen as well as chemical intermediate in the biosynthesisof othersteroid hormones, including the corticosteroids and the androgens and the estrogens.

It is derived from progesterone via 17-hydroxylase, a P450c17 enzyme, or from 17-hydroxypregnenolone via 3β-hydroxysteroid dehydrogenase isomerase.

17-OHP increases in the third trimester of pregnancy primarily due to fetal adrenal production.This steroid is primarily produced in the adrenal glands and to some degree in the gonads, specifically the corpus luteum of the ovary. Normal levels are 3-90 ng/dl in children, and in women, 20-100 ng/dl prior to ovulation, and 100-500 ng/dl during theluteal phase.

The hormone 17-hydroxyprogesterone is a building block for producing the hormone cortisol. Cortisol is produced mainly by the adrenal cortex (the outer part of the two adrenal glands, located above the kidneys). Cortisol is called thestress hormonebecause it’s secreted in larger amounts as part of the body’s response to physical or emotional stress.In kids, the most common cause of cortisol deficiency, and consequently high levels of 17-hydroxyprogesterone, is one of the forms of the genetic disorder congenital adrenal hyperplasia (CAH).

17-hydroxyprogesterone is elevated in patients with congenital adrenal hyperplasia (CAH). CAH is a group of autosomal recessive diseases characterized by a deficiency of cortisol and an excess of ACTH concentration. 17-hydroxyprogesterone is also useful in monitoring cortisol replacement therapy and in evaluating infertility and adrenal and ovarian neoplasms.

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