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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T18612 |
Bestatin-amido-Me
PROTAC IAP binding moiety 1 |
Others | Others |
Bestatin-amido-Me, a derivative of Bestatin, acts as an IAP ligand and interacts with ABL inhibitor through a linker to produce SNIPER[1]. | |||
T38470 |
Obestatin (human)
|
||
Obestatin (human) 是一种由 preproghrelin 经过剪切形成的G蛋白欧联实体39的内源性配体,可以剂量依赖的方式抑制进食,可用于研究肥胖。 | |||
TP2279L |
Obestatin (rat) acetate
|
GHSR | GPCR/G Protein |
Obestatin (rat) acetate 是 G 蛋白偶联受体 39 (GPR39) 的内源性配体。它具有抗炎、抗心肌梗塞和抗氧化特性。 它抑制食物摄入,抑制空肠收缩,并减少体重增加。 | |||
T25573 |
Ketomethylenebestatin
|
||
Ketomethylenebestatin is a carba-analog of bestatin,the aminopeptidase (AP) inhibitor. Ketomethylenebestatin is 10 fold less effective as an inhibitor of aminopeptidases than bestatin. | |||
T29436 | 4-Hydroxybestatin | ||
4-Hydroxybestatin is a major active metabolite of bestatin. | |||
T71626 |
Epibestatin Hydrochloride
|
||
Epibestatin Hydrochloride is a stabilizer of 14-3-3 PPIs, as well as a diastereoepimer of aminopeptidase inhibitor bestatin. | |||
T81626 |
Obestatin(11-23)mouse, rat
|
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Obestatin(11-23)mouse, rat 是多肽,涉及能量平衡调节,抑制摄食。该化合物能使啮齿类动物食量减少、体重降低、及空肠收缩。 | |||
T35787 |
Obestatin (human) (trifluoroacetate salt)
|
||
Obestatin is a 23 amino acid peptide hormone with a conserved C-terminal glycine residue and amidation site that is formed by cleavage of the ghrelin and obestatin prepropeptide.1It binds to the orphan receptor GPR39 (Kd= 1 nM) and stimulates cAMP production in CHO and HEK293 cells overexpressing human GPR39. Obestatin inhibits contraction of isolated mouse jejunum muscle strips induced by ghrelin .In vivo, obestatin (12.5-1,000 nmol/kg) suppresses food intake in a time- and dose-dependent manne... | |||
T75901 |
Obestatin(rat) TFA
|
||
Obestatin(rat) TFA 是一个包含23个氨基酸的肽,由Ghrelin基因编码。该化合物能够抑制食欲和空肠收缩,并能减缓体重增加。同时,Obestatin(rat) TFA 作为G 蛋白偶联受体 39 (GPR39) 的内源性配体,发挥抗炎、抗心肌梗塞和抗氧化功能。 | |||
TP2279 |
Obestatin(rat)
Obestatin (rat) |
Others | Others |
Endogenous peptide that suppresses food intake and body weight-gain | |||
T81625 |
Obestatin(human) TFA
|
||
Obestatin(human) TFA, 同源于与ghrelin相同的前体多肽,是一种内源性肽。该化合物抑制大鼠食欲并降低体重增加。 | |||
T18684 | SNIPER(ABL)-013 | Others | Others |
SNIPER(ABL)-013, conjugating GNF5 (ABL inhibitor) to Bestatin (IAP ligand) with a linker, induces the reduction of BCR-ABL protein with a DC50 of 20 μM[1]. | |||
T18650 |
Ch55-O-C3-NH2
RAR ligand 1 |
Others | Others |
Ch55-O-C3-NH2, also known as RAR ligand 1, is a ligand derived from the Ch55 compound that specifically targets RAR. Through a linker, Ch55-O-C3-NH2 interacts with cIAP1 ligand Bestatin to form SNIPER[1]. | |||
T17940 |
Estrone-N-O-C1-amido
ERα ligand 1 |
Others | Others |
Estrone-N-O-C1-amido (ERα ligand 1) is an estrogen ligand derived from Estrone that specifically binds to estrogen receptor α (ERα). Through a linker, Estrone-N-O-C1-amido (ERα ligand 1) forms a complex with the cIAP1 ligand Bestatin, leading to the creation of SNIPER[1]. | |||
T18687 |
SNIPER(ABL)-020
|
Others | Others |
SNIPER(ABL)-020 is a chemical compound consisting of Dasatinib, an ABL inhibitor, and Bestatin, an IAP ligand, conjugated with a linker. This compound effectively reduces the BCR-ABL protein[1]. | |||
T17545 | Biotin-BS | Others | Others |
Biotin-BS is a chemical compound composed of two distinct ligands: methyl-bestatin (MeBS) for cIAP1 and biotin. These ligands are interconnected through linkers. MeBS serves as a ligand specifically for the cellular inhibitor of apoptosis protein 1 (cIAP1) ubiquitin ligase[1]. | |||
T18693 |
SNIPER(ABL)-049
|
Others | Others |
SNIPER(ABL)-049, conjugating Imatinib (ABL inhibitor) to Bestatin (IAP ligand) with a linker, induces the reduction of BCR-ABL protein with a DC50 of 100 μM[1]. | |||
T18691 |
SNIPER(ABL)-044
|
Others | Others |
SNIPER(ABL)-044, conjugating HG-7-85-01 (ABL inhibitor) to Bestatin (IAP ligand) with a linker, induces the reduction of BCR-ABL protein with a DC50 of 10 μM[1]. | |||
T14288 | Androstanolone acetate | Others | Others |
Androstanolone acetate is a compound that functions as an androgen ligand, specifically targeting the androgen receptor (AR). It binds to the cIAP1 ligand Bestatin through a linker, resulting in the formation of PROTACs[1]. | |||
T17706 | BzNH-BS | Others | Others |
BzNH-BS is a chemical compound comprising two distinct ligands: methyl-bestatin (MeBS) for cIAP1 and benzoyl-amide. The ligands are interconnected through linkers. MeBS functions as a ligand for cIAP1, a ubiquitin ligase involved in cellular inhibition of apoptosis processes [1]. | |||
T17733 |
ATRA-hydroxyimino
CRABP-II ligand 1 |
Others | Others |
ATRA-hydroxyimino, also known as CRABP-II ligand 1, is a chemical compound derived from Retinoic acid (ATRA). This compound binds to the cIAP1 ligand, specifically Bestatin, through a linker, resulting in the formation of a complex called SNIPER. The purpose of this complex is to degrade CRABP-II within IMR-32 cells[1]. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1257 |
Bestatin
Ubenimex,乌苯美司 |
Others; Aminopeptidase; Antibacterial; Antibiotic; LTR | Immunology/Inflammation; Metabolism; Microbiology/Virology; Others |
Bestatin (Ubenimex) 是 CD13 (Aminopeptidase N)/APN 和 leukotriene A4 hydrolase 抑制剂,可用于癌症研究。 | |||
T3529 |
Bestatin hydrochloride
盐酸乌苯美司,Ubenimex hydrochloride,苯丁抑制素 |
Integrin; Aminopeptidase; Antibacterial; Antibiotic | Cytoskeletal Signaling; Metabolism; Microbiology/Virology |
Bestatin hydrochloride (Ubenimex hydrochloride) 是CD13(Aminopeptidase N)/APN 和leukotriene A4 hydrolase 抑制剂,可研究癌症。 | |||
T62258 |
Bestatin trifluoroacetate
|
||
Bestatin trifluoroacetate (Ubenimex trifluoroacetate) 是一种 CD13 (Aminopeptidase N)/APN 和 leukotriene A4 hydrolase 抑制剂,经常用于研究癌症。 |