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Search Results for " c57bl/6j mice "
Targets Recommended: GPCR19

5

抑制剂 & 化合物

2

天然产物

2

重组蛋白

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Cat. No. Product Name Target Signaling Pathways
T1824 TGR5 Receptor Agonist

GPCR19 GPCR/G Protein
TGR5 Receptor Agonist 是一种TGR5(GPCR19)激动剂。
T63584 ATX inhibitor 12

Others Others
ATX inhibitor 12 是口服具有活力的 ATX 抑制剂 (IC50: 1.72 nM)。在 C57Bl/6J 小鼠中,口服剂量为 60 mg/kg 的 ATX inhibitor 12 时,能够有效抑制肺结构损伤,降低纤维化病变。ATX inhibitor 12 能够用于研究特发性肺纤维化 (IPF) 。
T23945 DA-11004

DA11004,UNII-48M66E9ER2

Others Others
DA-11004 is a potent NADP-dependent isocitrate dehydrogenase inhibitor (IC50: 1.49 μM for IDPc). DA-11004 inhibited fatty acid synthesis in adipose tissues via IDPc inhibition. It also decreased the plasma glucose levels and FFA in HF diet-induced obesity
T15043 D5D-IN-326

Others Others
D5D-IN-326 is an orally active delta-5 desaturase (D5D) inhibitor (IC50s: 72 and 22 nM for rat and human D5D in enzymic and cell-based assays). It has no effect on D6D or D9D activity. D5D-IN-326 reduces insulin resistance and decreases body weight in die
T36296 BIO5192 hydrate

Others Others
BIO5192 hydrate is a selective and potent integrin α4β1 (VLA-4) inhibitor (Kd<10 pM). BIO5192 hydrate selectively binds to α4β1 (IC50=1.8 nM) over a range of other integrins. BIO5192 hydrate results in a 30-fold increase in mobilization of murine hematopoietic stem and progenitors (HSPCs) over basal levels[1][2]. The combination of BIO5192 hydrate (1 mg/kg; i.v.) and Plerixafor (5 mg/kg; s.c.) exert an additive effect on progenitor mobilization[1].BIO5192 hydrate (30 mg/kg; s.c; bid; during days...

化合物

TGR5 Receptor Agonist
Cat.No: T1824
Synonym:
Target: GPCR19
ATX inhibitor 12
Cat.No: T63584
Synonym:
Target: Others
DA-11004
Cat.No: T23945
Synonym: DA11004,UNII-48M66E9ER2
Target: Others
D5D-IN-326
Cat.No: T15043
Synonym:
Target: Others
BIO5192 hydrate
Cat.No: T36296
Synonym:
Target: Others
Cat. No. Product Name Target Signaling Pathways
T7036 2,4'-Dihydroxybenzophenone

Antioxidant oxidation-reduction
2,4'-Dihydroxybenzophenone 可有效保护 C57BL/6J 小鼠免受 APAP 诱导的肝毒性。它对可卡因诱导的小鼠急性肝毒性和神经毒性具有保护作用。其机制可能与其抗氧化活性有关。
T30451 Biliatresone

Others Others
Biliatresone 是一种从球藻 Dysphania glomulifera 和 D. littoralis 中分离出来的环境毒素,诱导 C57BL/6J 新生儿胆管病,诱导谷胱甘肽 (GSH) 水平降低,诱导 SOX17 胆管细胞水平显着降低,诱导小鼠肝外胆管细胞损伤和纤维化。

天然产物

2,4'-Dihydroxybenzophenone
Cat.No: T7036
Synonym:
Target: Antioxidant
Biliatresone
Cat.No: T30451
Synonym:
Target: Others
Cat. No. Product Name Species Expression System
TMPY-02686 PON3 Protein, Human, Recombinant (S50N, His)

paraoxonase 3

Human Baculovirus Insect Cells
PON3 was enriched in the mitochondria-associated membrane fraction of hepatocytes. PON3 deficiency resulted in impaired mitochondrial respiration, increased mitochondrial superoxide levels, and increased hepatic expression of inflammatory genes. PON3 deficiency did not influence atherosclerosis development on an apolipoprotein E null hyperlipidemic background, but it did lead to a significant 60% increase in atherosclerotic lesion size in Pon3KO mice on the C57BL/6J background when fed a cholate...
TMPJ-01106 NAD(P) transhydrogenase/NNT Protein, Human, Recombinant (His)

NAD(P) transhydrogenase,NNT

Human E. coli
NAD(P)+transhydrogenase (NNT) is located in the inner mitochondrial membrane and catalyzes a reversible hydride transfer between NAD(H) and NADP(H) that is coupled to proton translocation between the intermembrane space and mitochondrial matrix. NNT activity has an essential role in maintaining the NADPH supply for antioxidant defense and biosynthetic pathways. Structurally, NNT is composed of three domains; domains I and III are hydrophilic and have binding sites for NAD and NADP, respectively,...

重组蛋白

PON3 Protein, Human, Recombinant (S50N, His)
Cat.No: TMPY-02686
Species: Human
Expression System: Baculovirus Insect Cells
NAD(P) transhydrogenase/NNT Protein, Human, Recombinant (His)
Cat.No: TMPJ-01106
Species: Human
Expression System: E. coli
TargetMol Loading
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