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T7132(Rac)-BrassinazoleCytochrome P450,brassinosteroid,(Rac)Brassinazole,triazole-type,CYP90B,CYPs,biosyn
Brassinosteroids are a class of phytohormones with essential roles in plant growth and development, including the promotion of stem elongation and cell division. Brassinazole is a triazole-type brassinosteroid biosynthesis inhibitor.
价 格：￥电议型 号：T7132产 地：中国大陆
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T6653Salmeterol Xinafoatecorticosteroid,Salmeterol,Beta Receptor,therapy,inhibit,Adrenergic Receptor,GR 3
Salmeterol Xinafoate is a long-acting β2-adrenergic receptor agonist with anti-inflammatory effects, used in the treatment of asthma symptoms and chronic obstructive pulmonary disease (COPD) symptoms.
价 格：￥电议型 号：T6653产 地：中国大陆
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TP1031TetracosactideTetracosactide,adrenal gland,adrenocorticotrophic hormone,Inhibitor,corticosteroids,in
Tetracosactide (INN) is a synthetic peptide that is identical to the 24-amino acid segment (sequence: SYSMEHFRWGKPVGKKRRPVKVYP) at the N-terminal of adrenocorticotropic hormone.
价 格：￥电议型 号：TP1031产 地：中国大陆
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T6737ZaltoprofenCN-100,anti-inflammatory,COX-2,inhibit,non-steroidal,Zaltoprofen,Inhibitor,COX,NSAID,COX-
Zaltoprofen is a Cox-1 and Cox-2 inhibitor, which is used for the treatment of arthritis.
价 格：￥电议型 号：T6737产 地：中国大陆
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T36683VedaprofenVedaprofen,Inhibitor,nonsteroidal,PM150,PM-150,Escherichia coli,inhibit,CERM-10202,CERM102
Vedaprofen inhibits COX-1 and reduces prostaglandin H2 synthesis with anti-inflammatory activities. Vedaprofen is an inhibitor of Escherichia coli sliding clamp with the IC50 of 222 μM and Ki of 131 μM.
价 格：￥电议型 号：T36683产 地：中国大陆
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TN1807IsoverticineIsoverticine,cytotoxicity,alkaloid,isosteroidal,Inhibitor,antitumor,inhibit
Isoverticine exhibits significant antitussive, expectorant and anti-inflammatory activities, it also displays significant cytotoxicity.
价 格：￥电议型 号：TN1807产 地：中国大陆
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T8575ENFENAMIC ACIDnonsteroidal,wound healing,Inhibitor,suppress,RH-8,RH8,inhibit,RH 8,ENFENAMIC ACID,ant
Enfenamic acid is a platelet aggregation inhibitor and with antirheumatic.
价 格：￥电议型 号：T8575产 地：中国大陆
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T28362PF-02413873nonsteroidal,inhibit,PF 2413873,Progesterone Receptor,endometrial,PF-2413873,nuclear,PF 0
PF-02413873 is a competitive antagonist of nonsteroidal progesterone receptor with a Ki of 2.6 nM. PF-02413873 can be used in studies about the treatment of gynecological conditions such as endometriosis.
价 格：￥电议型 号：T28362产 地：中国大陆
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T2S0410Euphorbia factor L1Euphorbiasteroid；大戟因子L1；大戟因子 L1
1. Euphorbia factor L1 can enhance the ATP hydrolysis activity of ABCB1 stimulated by verapamil. 2. Euphorbia factor L1 inhibits the efflux of ABCB1 in KBv200 and MCF-7/adr cells, does not downregulate their expression either in mRNA or protein level.
价 格：￥电议型 号：T2S0410产 地：中国大陆
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T83752Biotin-SRC-1 (676–700) TFA；化合物 Biotin-SRC-1 (676–700) TFABiotin-Steroid Receptor Coactivator 1 (676-
Biotin-SRC-1 (676–700), a biotinylated and truncated variant of steroid receptor coactivator 1 (SRC-1), finds application in affinity-based reporter assays such as time-resolved FRET (TR-FRET) and amplified luminescent proximity homogenous assay (ΑLPHASCREEN?).
价 格：￥电议型 号：T83752产 地：中国大陆
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T81092Steroid sulfatase/17β-HSD1-IN-5；化合物 Steroid sulfatase/17β-HSD1-IN-5Steroid sulfatase/17β-HSD1-IN-5
Steroid sulfatase/17β-HSD1-IN-5 serves as an irreversible inhibitor of steroid sulfatase (STS) and a reversible, selective inhibitor of 7β-hydroxysteroid dehydrogenase type1 (17β-HSD1), exhibiting IC50 values of 43 nM for 17β-HSD1 and 6.2μM for 17β-HSD2. This compound is utilized in research related to metabolic diseases, particularly endometriosis [1].
价 格：￥电议型 号：T81092产 地：中国大陆
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T81091Steroid sulfatase-IN-5；化合物 Steroid sulfatase-IN-5Steroid sulfatase-IN-5
Steroid sulfatase-IN-5 (compound 10b), an inhibitor of steroid sulfatase (STS) with an IC50 of 0.32 nM, effectively suppresses T-47D breast cancer cell proliferation, demonstrating an IC50 value of 35.7 μM. This compound is utilized in breast cancer research [1].
价 格：￥电议型 号：T81091产 地：中国大陆
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T81090Steroid sulfatase-IN-6；化合物 Steroid sulfatase-IN-6Steroid sulfatase-IN-6
Steroid Sulfatase-IN-6 (Compound 10c) serves as an irreversible steroid sulfatase (STS) inhibitor, exhibiting a K i value of 0.4 nM against human placenta STS, and is applicable in tumor disease research [1].
价 格：￥电议型 号：T81090产 地：中国大陆
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T81089Steroid sulfatase-IN-7；化合物 Steroid sulfatase-IN-7Steroid sulfatase-IN-7
Steroid sulfatase-IN-7 is an irreversible inhibitor of steroid sulfatase (STS), demonstrating potent activity with an IC50 of 0.05 nM against human placental STS, rendering it suitable for application in cancer research [1].
价 格：￥电议型 号：T81089产 地：中国大陆
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T761473α-Hydroxysteroid dehydrogenase；化合物 3α-Hydroxysteroid dehydrogenase3α-Hydroxysteroid dehydrogenase
3α-Hydroxysteroid dehydrogenase (3α-HSD), encoded by the AKR1C4 gene, is responsible for catalyzing the transformation of 3-ketosteroids into 3α-hydroxy compounds. This enzyme significantly contributes to the inactivation of the androgen DHT by converting it into 3α-androstanediol, which exhibits reduced androgen activity. Such conversions are crucial in hirsutism research [1].
价 格：￥电议型 号：T76147产 地：中国大陆
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T62237Steroid sulfatase-IN-4；化合物 Steroid sulfatase-IN-4Steroid sulfatase-IN-4
Steroid sulfatase-IN-4 (Compound 16) is an irreversible inhibitor of steroid sulfatase (STS) that acts on human STS (IC50: 25 nM). steroid sulfatase-IN-4 can be used to study endometriosis.
价 格：￥电议型 号：T62237产 地：中国大陆
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T62236Steroid sulfatase/17β-HSD1-IN-3；化合物 Steroid sulfatase/17β-HSD1-IN-3Steroid sulfatase/17β-HSD1-IN-3
Steroid sulfatase/17β-HSD1-IN-3 (compound 19) is a dual inhibitor of steroid sulfatase (STS) and 17β-hydroxysteroid dehydrogenase type 1 (17β HSD1). Steroid sulfatase/17β-HSD1-IN-3 can be used to study endometriosis and other estrogen-dependent diseases.
价 格：￥电议型 号：T62236产 地：中国大陆
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T61979Steroid sulfatase/17β-HSD1-IN-4；化合物 Steroid sulfatase/17β-HSD1-IN-4Steroid sulfatase/17β-HSD1-IN-4
Steroid sulfatase/17β-HSD1-IN-4 (compound 37) is a potent dual inhibitor of steroid sulfatase ( STS ) and 17β-hydroxysteroid dehydrogenase type 1 ( 17β HSD1 ). Steroid sulfatase/17β-HSD1-IN-4 irreversibly inhibits hSTS activity (IC50= 63 nM). Steroid sulfatase/17β-HSD1-IN-4 has research value in endometriosis and other estrogen-dependent diseases.
价 格：￥电议型 号：T61979产 地：中国大陆
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T61716Steroid sulfatase/17β-HSD1-IN-1；化合物 Steroid sulfatase/17β-HSD1-IN-1Steroid sulfatase/17β-HSD1-IN-1
Steroid sulfatase/17β-HSD1-IN-1 is a highly effective inhibitor of both steroid sulfatase and 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1) activities, displaying an IC50 value of 28 nM against cellular human steroid sulfatase. This compound holds significant potential for investigating estrogen-dependent diseases [1].
价 格：￥电议型 号：T61716产 地：中国大陆
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T61687Steroid sulfatase-IN-1；化合物 Steroid sulfatase-IN-1Steroid sulfatase-IN-1
Steroid sulfatase-IN-1 is a highly potent and orally active inhibitor of the enzyme Steroid sulfatase, with an impressive IC50 value of 1.71 μM. This compound exhibits notable antitumor activity, achieving a TGI (tumor growth inhibition) of 51% in vivo. Therefore, Steroid sulfatase-IN-1 holds great promise in the field of breast cancer research [1].
价 格：￥电议型 号：T61687产 地：中国大陆
