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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T9509 | Methyl 2-hydroxy-4-methylvalerate | Others | |
Methyl 2-hydroxy-4-methylvalerate is one of dominant volatile compounds in Zhenjiang aromatic vinegar. | |||
T65873 | 2-Methylcinnamic acid, predominantly trans | ||
2-Methylcinnamic acid, predominantly trans is a useful organic compound for research related to life sciences. The catalog number is T65873 and the CAS number is 2373-76-4. | |||
T67378 | 3-Bromocinnamic acid, predominantly trans | ||
3-Bromocinnamic acid, predominantly trans is a useful organic compound for research related to life sciences and the catalog number is T67378. | |||
T67479 | 3,5-Dimethoxycinnamic acid, predominantly trans | ||
3,5-Dimethoxycinnamic acid, predominantly trans is a useful organic compound for research related to life sciences. The catalog number is T67479 and the CAS number is 16909-11-8. | |||
T25372 | EMD57033 | EMD-57033,(+)-EMD 57033,EMD 57033 | Calcium Channel , Carbonic Anhydrase |
EMD57033 is a cardiac troponin C (cTnC) activator, a dominant Ca2+ sensitizer, which functions by binding to cardiac/slow skeletal troponin C heterodimers to promote cardiac contraction. | |||
T22282 | Brr2-IN-3 | Brr2 Inhibitor 9,Brr2 Inhibitor C9 | Others |
Brr2-IN-3 (Brr2 Inhibitor C9) is an allosteric inhibitor of the spliceosomal RNA helicase Brr2. Brr2 is implicated in autosomal-dominant retinitis pigmentosa (a group of progressive retinal degenerative disorders). | |||
T4858 | 4-Hydroxyphenylpyruvic acid | 4-Hydroxyphenylpyruvic acid | Endogenous Metabolite |
4-Hydroxyphenylpyruvic acid is an enzyme inhibitor.4-Hydroxyphenylpyruvic acid (4-HPPA) is a keto acid that is involved in the tyrosine catabolism pathway. It is a product of the enzyme (R)-4-hydroxyphenyllactate dehydro... | |||
TP1755 | Ac-MBP (1-11) | Ac-MBP 1-11 | |
Ac-MBP 1-11, a primary encephalitogenic epitope in myelin basic protein (MBP), is a dominant short peptide sequence[1]. | |||
T32072 | Hexyl decanoate | Decanoic acid hexyl ester | |
Hexyl decanoate, the first trail pheromone compound identified in a stingless bee, Trigona recursa. Hexyl decanoate is dominant component of gland secretions. | |||
T28409 | Photoregulin1 | ||
Photoregulin1 is a modulator of Nr2e3. Photoregulin1 slows the progression of photoreceptor degeneration in two common mouse models of autosomal dominant RP, the RhoP23H and the Pde6brd1 mutations. | |||
T39712 | RGLS4326 | RG4326,RGLS4326 | |
RGLS4326 (RG4326) is a short oligonucleotide inhibitor of microRNA-17 (miR-17), with a pioneering role in its class. This compound, with a research focus on autosomal dominant polycystic kidney disease (ADPKD), effective... | |||
T64174 | Vasopressin V2 receptor antagonist 1 | ||
Vasopressin V2 receptor antagonist 1 (Compound 4g) is a vasopressin V2receptor (V2R) antagonist (Ki: 3.8 nM). dominant polycystic kidney disease (ADPKD). | |||
T39105 | Ibiglustat succinate | GZ402671succinate,Venglustat succinate,Ibiglustat succinate,SAR402671succinate | |
Ibiglustat (Venglustat) succinate is an orally active, brain-penetrant inhibitor of glucosylceramide synthase (GCS). It is utilized in the investigation of Gaucher disease type 3, Parkinson's disease associated with GBA ... | |||
T76419 | Protein Kinase C γ Peptide | ||
Protein Kinase C (gamma) Peptide, a fragment of Protein Kinase Cγ, plays a role in dominant ataxia by inhibiting the nuclear import of aprataxin, which is associated with recessive ataxia [1]. | |||
T61362 | CDK5-IN-3 | ||
CDK5-IN-3 (compound 11) is a highly potent and selective inhibitor of CDK5, demonstrating significant inhibition with IC50 values of 0.6 nM and 18 nM for CDK5/p25 and CDK2/CycA, respectively. This compound holds promise ... | |||
T73163 | CDK7-IN-20 | ||
CDK7-IN-20 is a potent, selective, and irreversible inhibitor of Cyclin-Dependent Kinase 7 (CDK7) with an IC50 value of 4 nM, exhibiting over 206-fold selectivity against related kinases CDK1, CDK2, CDK3, CDK5, CDK6, CDK... | |||
T83508 | [Arg6]-β-Amyloid (1-42), england mutation | ||
[Arg6]-β-Amyloid (1-42), England mutation, is a biologically active peptide associated with autosomal dominant Alzheimer's Disease in various kindreds. The English (H6R) mutation disrupts H6 interactions due to several m... | |||
T73289 | MHTT-IN-1 | ||
mHTT-IN-1 (Example 1) is a potent inhibitor of the mutant huntingtin protein (mHTT), which is toxic and primarily responsible for Huntington's disease (HD), an inherited autosomal dominant neurodegenerative disorder. Thi... | |||
T81431 | Pol (476-484), HIV-1 RT Epitope | ||
Pol (476-484), HIV-1 RT Epitope is a biologically active peptide and represents the dominant HLA A*0201-restricted epitope within HIV-1 reverse transcriptase (RT), spanning Pol residues 476-484. It has been utilized to e... | |||
T83509 | [Arg6]-β-Amyloid (1-40), england mutation | ||
β-Amyloid (1-40), England mutation, is a biologically active peptide with a histidine (His) to arginine (Arg) substitution at position 6, known to enhance oligomerization kinetics that serve as fibril seeds and increase ... |