242 Results for "

" in MedChemExpress (MCE) Product Catalog:
Products (242)

242 Results for "" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-13613
CAS No.: 164656-23-9
Purity:  99.83%
Synonyms: GG 745; GI 198745
Research Areas:  

Cancer

Dutasteride (GG745) is a potent inhibitor of both -reductase isozymes. Dutasteride may possess off-target effects on the androgen receptor (AR) due to its structural similarity to DHT .
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5
5 Cited Publications
Cat. No.: HY-14571
CAS No.: 289483-69-8
Purity:  99.06%
Synonyms: ER68203-00
Research Areas:  

Infection Metabolic Disease Cancer

E7820 (ER68203-00), an orally active aromatic sulfonamide derivative, is a molecular glue that induces the targeted degradation of splicing factor RBM39 by recruiting the E3 ubiquitin ligase CUL4-RBX1-DDB1-DCAF15 (CRL4 DCAF15). E7820 is an angiogenesis inhibitor suppressing an expression of integrin alpha2 subunit on endothelium. E7820 inhibits rat aorta angiogenesis with an IC50 of 0.11 μg/ml. E7820 modulates α-1, α-2, α-3, and α-5 integrin mRNA expression. E7820 can be used for the study of acute myeloid leukemia (AML) .
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4
4 Cited Publications
Cat. No.: HY-13635
CAS No.: 98319-26-7
Purity:  99.97%
Synonyms: MK-906
Research Areas:  

Cancer

Finasteride (MK-906) is an orally active and competitive 5α-reductase inhibitor, with an IC50 of 4.2 nM for type II -reductase. Finasteride has approximately a 100-fold greater affinity for type II -reductase enzyme than for the type I enzyme. Finasteride can be used for the research of benign prostatic hyperplasia (BPH) and androgenic alopecia .
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3
3 Cited Publications
Cat. No.: HY-B0172A
CAS No.: 2276-93-9
Synonyms: 3β-Hydroxy--cholanic acid
Target:  

Drug Derivative

Research Areas:  

Inflammation/Immunology

Isoallolithocholic acid (3β-Hydroxy-5α-cholanic acid), a derivative of Lithocholic acid (HY-10219), is a T cell regulator. Isoallolithocholic acid enhances regulatory T cells (Tregs) differentiation .
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3
3 Cited Publications
Cat. No.: HY-P7257
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CCL4; Act-2; Prev. SCYA4; MIP1B; Prev. LAG1; HC21; MIP-1-Beta; Monocyte Adherence-Induced Protein 5 Alpha; AT744.1; Chemokine C-C Motif Ligand 4; Small Inducible Cytokine A4 (Homologous To Mouse Mip-1b); Small-Inducible Cytokine A4; Macrophage Inflammator
Species:  
Source:  
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2
2 Cited Publications
Cat. No.: HY-N0440
CAS No.: 6902-91-6
Germacrone is a sesquiterpene compound with multiple biological activities. Germacrone inhibits the H1N1 and H3N2 influenza A virus and the influenza B virus. Germacrone blocks the progressionof arthritis by regulating Th1/Th2 balance and inhibiting NF-κB signaling. Germacrone can arrest the cell cycle at G0/G1 and G2/M phases and induce apoptosis in breast cancer cells. Germacrone inhibits 5α-reductase and has anti-androgenic effect. Germacrone has neuroprotective functions and can be used for the study of traumatic brain injury (TBI). Germacrone also has antioxidant activity [5].
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1
1 Cited Publications
Cat. No.: HY-135794
CAS No.: 32694-37-4
Purity:  ≥98.0%
Synonyms: 11-KDHT; -Dihydro-11-keto testosterone
Target:  

Androgen Receptor

Research Areas:  

Endocrinology

11-Ketodihydrotestosterone (11-KDHT; -Dihydro-11-keto testosterone) is an endogenous steroid and a metabolite of 11β-Hydroxyandrostenedione. 11-Ketodihydrotestosterone is an active androgen and is also a potent androgen receptor (AR) agonist with a Ki of 20.4 nM and an EC50 of 1.35 nM for human AR. 11-Ketodihydrotestosterone drives gene regulation, protein expression and cell growth in androgen-dependent prostate cancer cells .
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1
1 Cited Publications
Cat. No.: HY-B0141A
CAS No.: 57-91-0
Synonyms: Alfatradiol; Epiestradiol; Epiestrol
Alpha-Estradiol is a weak estrogen and a 5α-reductase inhibitor which is used as a topical medication in the treatment of androgenic alopecia.
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1
1 Cited Publications
Cat. No.: HY-P71889
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CCL4; Act-2; Prev. SCYA4; MIP1B; Prev. LAG1; HC21; MIP-1-Beta; Monocyte Adherence-Induced Protein 5 Alpha; AT744.1; Chemokine C-C Motif Ligand 4; Small Inducible Cytokine A4 (Homologous To Mouse Mip-1b); Small-Inducible Cytokine A4; Macrophage Inflammator
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Source:  
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1
1 Cited Publications
Cat. No.: HY-P77718
Purity:  ≥ 95%, as determined by reducing SDS-PAGE or Bis-Tris PAGE.
Synonyms: ITGA5; Integrin Alpha-F; Prev. FNRA; CDNA FLJ50382, Moderately Similar To Integrin Alpha-5; CD49e; Very Late Activation Protein 5, Alpha Subunit; Integrin, Alpha 5 (Fibronectin Receptor, Alpha Polypeptide); Fibronectin Receptor, Alpha Subunit; Fibronectin
Species:  
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Cat. No.: HY-107819
CAS No.: 80-97-7
Purity:  99.92%
Synonyms: Dihydrocholesterol; -Cholestanol; NSC 18188
-Cholestan-3β-ol is a derivitized steroid compound.
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Cat. No.: HY-N2489
CAS No.: 56786-63-1
Synonyms: Brassinosteroid BB 16; DI 31
Research Areas:  

Others

-Hydroxy-laxogenin (Brassinosteroid BB 16; DI 31) is a derivative of laxogenin, a spirostane-type steroid. -Hydroxy-laxogenin serves as a plant-derived anabolic agent and is used as a dietary supplement .
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Cat. No.: HY-133971
CAS No.: 1250-95-9
Purity:  98.40%
Synonyms: ,6α-Epoxycholesterol
Cholesterol-5α,6α-epoxide is an epoxide derivative of cholesterol formed by the enzymatic oxidation of cholesterol in the liver and other tissues. Cholesterol-5α,6α-epoxide has unique chemical properties that make it an important intermediate in the biosynthesis of bile acids, which play a key role in the digestion and absorption of dietary fats. It also has a potential physiological role in regulating cholesterol metabolism and transport, although its biological function is not fully understood.
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Cat. No.: HY-E70558
Target:  

5 alpha Reductase

Research Areas:  

Metabolic Disease

-reductase, Rat (Sprague-Dawley) Liver is an enzyme involved in steroid metabolism and participates in the androgen metabolic pathway. -reductase, Rat (Sprague-Dawley) Liver catalyzes the conversion of testosterone to -dihydrotestosterone (DHT). DHT plays important roles in the development of male sex organs, hair growth, prostate function, and other aspects .
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Cat. No.: HY-W677042
CAS No.: 1153-51-1
Synonyms: -Androst-16-en-3α-ol
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

α-Androstenol (-Androst-16-en-3α-ol) is a steroid pheromone that has been found in boar testes and male axillary sweat. α-Androstenol is also a positive allosteric modulator of GABAA receptors, which enhances GABA-activated currents in primary mouse cerebellar granule cells (EC50 of 0.4 μM). α-Androstenol produces anxiolytic-like, antidepressant-like, and anticonvulsant effects in mice. α-Androstenol can be used for the research of seizures .
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Cat. No.: HY-W013854
CAS No.: 1224-92-6
Synonyms: 3β-Hydroxy--androstane
Target:  

Endogenous Metabolite

Research Areas:  

Others

-Androstan-3β-ol (Androstan), a saturated sterol, is a CAR (constitutive androstane receptor) inverse agonist ligand. -Androstan-3β-ol (Androstan) increases the AmB-channel conductance in a concentration dependent manner .
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Cat. No.: HY-123349
CAS No.: 13027-33-3
Target:  

Drug Metabolite

Research Areas:  

Cardiovascular Disease

-Hydroxy-6-keto cholesterol is major metabolite of β-epoxide (5α,6β-epoxycholesterol) during direct exposure of intact cultured human bronchial epithelial cells (16-HBE) to ozone. -Hydroxy-6-keto cholesterol inhibits cholesterol synthesis with an IC50 of 350 nM .
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Cat. No.: HY-133970
CAS No.: 481-21-0
Purity:  99.34%
-Cholestane is a skeleton. -Cholestane can be used in the synthesis of Brassinosteroids. -Cholestane can be used in skeletal muscle research .
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Cat. No.: HY-124463
CAS No.: 567-01-1
Synonyms: ,3β-THDOC
Target:  

GABA Receptor iGluR

Research Areas:  

Neurological Disease

Epiallopregnanolone (5α,3β-THDOC), a 3β-hydroxy neurosteroid, an antagonist at GABAA receptors and a NMDA receptor enhancer .
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Cat. No.: HY-123489
CAS No.: 567-02-2
Purity:  ≥98.0%
Synonyms: THDOC
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

3α,21-Dihydroxy-5α-pregnan-20-one (THDOC), an endogenous neurosteroid, is a positive modulator of GABAA receptors. 3α,21-Dihydroxy-5α-pregnan-20-one potentiates neuronal response to low concentrations of GABA at α4β1δ GABAA receptors in vitro.
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