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    Home > Natural Products > Steroids (Find 100 items)

    Steroids

    Pregnenolone

    (145-13-1)
    1. Glucocortcoid, antiinflammatory
    2. Pregnenolone 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

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    Tigogenin

    (77-60-1)
    Used as a raw material for hormone drugs Raw materials for anordrin, dehydromethyltestosterone, Anadrol, etc.; used as raw materials for hormone drugs; sisal saponins are derived from hemp juice and hemp residue discarded after the production of traditional sisal fiber products The extracted natural plant saponins are pharmaceutical intermediates and important raw materials for the synthesis of steroid hormone drugs. They are widely used in the manufacture of more than 200 drugs in the three categories of adrenal cortex hormones, sex hormones and anabolic hormones.

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    Qingyangshengenin

    (84745-94-8)
    Qingyanshengenin (NSC 379666; compound 2), a pregnane glycoside, is a C21 steroidal aglycone isolated from the root of Cynanchumot ophyllum (Asclepiadaceae). Qingyanshengenin has anti-cancer activity[1].

    SOLASODINE

    (126-17-0)
    Starting material for steroidal drugs. A neuroprotective antioxidant glycoalkaloid that can increase brain tissue superoxide dismutase (SOD), catalase (CAT) and gluten in the rat brain ischemia-reperfusion (I/R) injury model. Glutathione (GSH) levels reduce lipid peroxidation (LPO) and nitric oxide (NO) levels.

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    caudatin

    (38395-02-7)
    Gaodating has inhibitory effects on the growth of human gastric cancer, colon cancer, lung cancer and other human tumor cell lines. Gaodating has anti-gastric cancer and liver cancer effects.

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    GLYCODEOXYCHOLICACID

    (360-65-6)
    Inducing apoptosis of liver cells may cause DNA division. Induces liver cell apoptosis and may cause DNA division. Biochemical research; lipase accelerator; ion remover, used for protein dissolution; preparation of bacterial culture medium (intestinal bacterial culture and separation); inducing hepatocyte apoptosis, possibly inducing DNA clearance

    (22E)-5α-Ergosta-7,22-dien-3β-ol

    (2465-11-4)
    One of the six sterols isolated from the fruiting bodies of Boletus pulverulentus Opat. (Boletaceae) and identified as (22E)-Ergosta-5,7,9(11),22-tetraen-3β-ol, Ergosterol, Ergosta-5,7-dien-3β-ol, (22E)-Ergosta-5,8,22-trien-3β-ol, (22E)-Ergosta-7,22-dien-3β-ol (Stellasterol), and Ergost-7-en-3β-ol.

    poriferasterol monoglucoside

    (19716-26-8)
    Stigmasterol glucoside is a sterol isolated from P. urinaria with high antioxidant and anti-inflammatory activities[1], act as an inhibitor of 5α-reductase with an IC50 of 27.2 µM[2].

    PONASTERONE A

    (13408-56-5)
    Ponasterone A is a steroid compound of ecdysone, which is widely distributed in nature, and people have been extremely interested in it very long ago. As early as 1919, biologist Polish proposed the mechanism of insect ecdysone. In 1954, Butenadt and Kalson separated α-ecdysone from the silkworm pupa. In 1966, Nakanishi, Horm and other insect plants were used to extract Pannasterone. Later, many countries at home and abroad successively proposed ecdysone from many materials. Ecdysone can promote the synthesis of nucleic acids and proteins, affect the metabolism of sugar, promote lipid metabolism, immune regulation, affect the central nervous system, treat rheumatism, arthritis, anti-oxidative stress, anti-tumor effect. The performance of Ponasterone in certain neurosensing systems is 3-100 times that of β-ecdysone (β-ecdysone).

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    Steroids are a general term for a large class of cyclopentanic fully hydrogenated phenanthrene derivatives widely distributed in the biological world. Also known as steroids and steroids. Steroid compounds do not contain bound fatty acids and are non-saponifiable lipids; these compounds are isoprenoid substances, which are generated by triterpene cyclization and then internal molecular reorganization and chemical modification. Steroids include steroids, bile acids and bile alcohols, steroid hormones, insect ecdysone, cardiac glycosides and saponins, and toad poison.
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