| Company Name: |
WUHAN SUN-SHINE BIO-TECHNOLOGY Co., Ltd.
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17702719238 17702719238 |
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sales@sun-shinechem.com |
| Products Intro: |
Product Name:GX-674
CAS:1432913-36-4
Purity:98% HPLC Package:50.0mg;100.0mg; 200.0mg;500mg;1g;5g; 10g
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| Company Name: |
BOC Sciences
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| Email: |
info@bocsci.com |
| Products Intro: |
Product Name:GX-674
CAS:1432913-36-4
Package:$998/5mg Remarks:GX-674 is a Nav1.7 antagonist in the aryl sulfonamide class with higher selectivity for Nav1.7 (IC50= 0.1nM) over other Nav subtypes. Nav1.7 is commonly expressed in olfactory epithelium, sympathetic
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| Product Name: | GX-674 | | Synonyms: | GX-674;GX-674; GX674;GX 674;Benzenesulfonamide, 4-[2-(2-amino-1H-benzimidazol-6-yl)-4-chlorophenoxy]-2,5-difluoro-N-1,2,4-thiadiazol-5-yl- | | CAS: | 1432913-36-4 | | MF: | C21H13ClF2N6O3S2 | | MW: | 534.95 | | EINECS: | | | Product Categories: | | | Mol File: | 1432913-36-4.mol |  |
| | GX-674 Chemical Properties |
| Boiling point | 734.8±70.0 °C(Predicted) | | density | 1.678±0.06 g/cm3(Predicted) | | solubility | Soluble in DMSO | | pka | 3.46±0.10(Predicted) |
| | GX-674 Usage And Synthesis |
| Biological Activity | gx-674 is an aryl sulfonamide class of antagonists that inhibits nav1.7 [1]nav (voltage-gated sodium) channels conduct ionic currents that initiate action potentials in neurons and muscles cells. human express 9 nav channel isoforms (nav 1.1-1.9), among which nav 1.7 channel are express in olfactory epithelium, sympathetic ganglion, and dorsal root ganglion sensory neurons. gain-of-function mutations in nav1.7 are associated with extreme pain disorders whereas loss-of-function mutations cause congenital insensitivity to pain in individuals. [1]in hek293 cells, patch clamp analysis was perform for human nav channels. gx-674 shows potent inhibition effect on nav.1.7 (ic50= 0.1nm). gx-674 also exhibits substantial selectivity on different nav subtypes. it shows much higher inhibitory effects on nav 1.7 over other nav isoform, such as 100000 times more potent for nav1.7 than for nav 1.5. gx-74 is also reported to bind to a high-affinity, isoform-selective, and extracellularly accessible site on vsd4. (i.e. one of the peripheral voltage-sensor domains of nav.1.7). [1] | | references | 1. ahuja s, mukund s, deng l et al. structural basis of nav1.7 inhibition by an isoform-selective small-molecule antagonist. science. 2015 dec 18;350(6267):aac5464. |
| | GX-674 Preparation Products And Raw materials |
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