| Purity: | 98 |
|---|---|
| Model Number: | C21H17F4NO3S2 |
| Brand Name: | NJ STERIOD |
| Usage: | Animal Pharmaceuticals |
| Grade Standard: | Medicine Grade |
| Type: | Auxiliaries and Other Medicinal Chemicals |
| Place of Origin: | China (Mainland) |
| EINECS No.: | C21H17F4NO3S2 |
| CAS No.: | 317318-84-6 |
| CAS: | 317318-84-6) |
Quick Details
Specifications
Product Description
99% Purity Sarms Powder GW-0742/GW 610742 CAS: 317318-84-6
Name: GW-0742
Other Name: GW610742
CAS: 317318-84-6
Molecular Formula: C21H17F4NO3S2
Formula Weight: 471.5
GW-0742 Form: solid
GW-0742 Color: white
GW-0742 Mp: 134.5-135.5 °C
GW-0742 Solubility DMSO: > 5 mg/mL
H2O: insoluble
GW-0742 Storage temp. 2-8°C
GW-0742 Description:
GW0742 is a high affinity PPAR-β/δ agonist reduces lung inflammation induced by bleomycin instillation in mice.
A high throughput screening campaign was conducted to identify small molecules with the ability to inhibit the interaction between the vitamin D receptor (VDR) and steroid receptor coactivator 2. These inhibitors represent novel molecular probes to modulate gene regulation mediated by VDR. The peroxisome proliferator-activated receptor δ (PPARδ) agonist GW0742 was among the identified VDR-coactivator inhibitors and has been characterized herein as a pan nuclear receptor antagonist at concentrations higher than 12.1 μM. The highest antagonist activity for GW0742 was found for VDR and the androgen receptor (AR). Surprisingly, GW0742 behaved as PPAR agonist/antagonist activating transcription at lower concentration and inhibiting this effect at higher concentrations. A unique spectroscopic property of GW0742 was identified as well. In the presence of rhodamine-derived molecules, GW0742+ increased fluorescence intensity and fluorescence polarization at an excitation wavelength of 595 nm and emission wavelength of 615 nm in a dose dependent manner. The GW0742-inhibited NR-coactivator binding resulted in a reduced expression of five different NR target genes in LNCaP cells in the presence of agonist. Especially VDR target genes CYP24A1, IGFBP-3 and TRPV6 were negatively regulated by GW0742. GW0742 is the first VDR ligand inhibitor lacking the secosteroid structure of VDR ligand antagonists. Nevertheless, the VDR-meditated downstream process of cell differentiation was antagonized by GW0742 in HL-60 cells that were pretreated with the endogenous VDR agonist 1,25-dihydroxyvitamin D3.
Sarms List:
You can ask us any question you doubt and we will reply within 12 hours.
Old tracking numbers of your country can be offered for your reference.
Variety of discreet packages can be offered for your choice, also we can give advice of which package and express is the safest to your country according to our years of experience.
All our deliveries are packaged plain without any descriptions or company names. None else know what is inside. The delivery success rate was 99% last year, the rest was mostly due to incorrect addresses(Such as a Russian gentleman who can't offer his address in English correctly)
Our Advantages:
Customer Feedback:
·Well everyone is loving your products so I will be doing business strictly with you going forward!
·Thank you for the wonderful customer service and great products!
·I did receive the parcel and brewed up the gear. From what I have seen, I am very impressed and pleased with your products.
·As usual your business is much liked. The melting temps of all the products seem fine. We truly LOVE the quickness and professional of your service and will continue a long relationship with you.
·Your products are top notch...
Name: GW-0742
Other Name: GW610742
CAS: 317318-84-6
Molecular Formula: C21H17F4NO3S2
Formula Weight: 471.5
GW-0742 Form: solid
GW-0742 Color: white
GW-0742 Mp: 134.5-135.5 °C
GW-0742 Solubility DMSO: > 5 mg/mL
H2O: insoluble
GW-0742 Storage temp. 2-8°C
GW-0742 Description:
GW0742 is a high affinity PPAR-β/δ agonist reduces lung inflammation induced by bleomycin instillation in mice.
A high throughput screening campaign was conducted to identify small molecules with the ability to inhibit the interaction between the vitamin D receptor (VDR) and steroid receptor coactivator 2. These inhibitors represent novel molecular probes to modulate gene regulation mediated by VDR. The peroxisome proliferator-activated receptor δ (PPARδ) agonist GW0742 was among the identified VDR-coactivator inhibitors and has been characterized herein as a pan nuclear receptor antagonist at concentrations higher than 12.1 μM. The highest antagonist activity for GW0742 was found for VDR and the androgen receptor (AR). Surprisingly, GW0742 behaved as PPAR agonist/antagonist activating transcription at lower concentration and inhibiting this effect at higher concentrations. A unique spectroscopic property of GW0742 was identified as well. In the presence of rhodamine-derived molecules, GW0742+ increased fluorescence intensity and fluorescence polarization at an excitation wavelength of 595 nm and emission wavelength of 615 nm in a dose dependent manner. The GW0742-inhibited NR-coactivator binding resulted in a reduced expression of five different NR target genes in LNCaP cells in the presence of agonist. Especially VDR target genes CYP24A1, IGFBP-3 and TRPV6 were negatively regulated by GW0742. GW0742 is the first VDR ligand inhibitor lacking the secosteroid structure of VDR ligand antagonists. Nevertheless, the VDR-meditated downstream process of cell differentiation was antagonized by GW0742 in HL-60 cells that were pretreated with the endogenous VDR agonist 1,25-dihydroxyvitamin D3.
Sarms List:
| AICAR | 2627-69-2 |
| Andarine (GTX-007)(S4) | 401900-40-0 |
| GW-501516/Cardarine | 317318-70-0 |
| LGD-4033 | 1165910-22-4 |
| MK-677 (Ibutamoren) | 15972-10-0 |
| MK-2866 (Ostarine) | 841205-47-8 |
| RAD-140 | 1182367-47-0 |
| SR9009 | 1379686-30-2 |
| SR9011 | 1379686-29-9 |
| YK11 | 366508-78-3,431579-34-9 |
You can ask us any question you doubt and we will reply within 12 hours.
Old tracking numbers of your country can be offered for your reference.
Variety of discreet packages can be offered for your choice, also we can give advice of which package and express is the safest to your country according to our years of experience.
All our deliveries are packaged plain without any descriptions or company names. None else know what is inside. The delivery success rate was 99% last year, the rest was mostly due to incorrect addresses(Such as a Russian gentleman who can't offer his address in English correctly)
Our Advantages:
| Best Quality |
Professional leading manufacturers in China. Strict quality control before products are allowed to sell. |
| Competitive Price |
Factory direct sales. Best prices you're sure to be satisfied. |
| Safe Packing |
Professional packing department which have more than 16 years experience in disguising packages |
| Fast Delivery |
Plenty in stock, delivery within 24 hours after the payment. Fast and secure delivery by DHL, TNT, FedEx, HKEMS, UPS, etc. |
| Payment | T/T, Western Union, Money Gram, Bitcoin. |
| Service |
Photos of parcel and tracking number offered timely; 24/7 online helpful service |
| Discount |
Specials are possible when client's order is big enough, including the discount policy |
Customer Feedback:
·Well everyone is loving your products so I will be doing business strictly with you going forward!
·Thank you for the wonderful customer service and great products!
·I did receive the parcel and brewed up the gear. From what I have seen, I am very impressed and pleased with your products.
·As usual your business is much liked. The melting temps of all the products seem fine. We truly LOVE the quickness and professional of your service and will continue a long relationship with you.
·Your products are top notch...

