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Cat. No. | Product Name | Target | Signaling Pathways |
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T7767 |
FMoc-Val-Cit-PAB-PNP
|
Others | Others |
Fmoc-Val-Cit-PAB-PNP 是一种可降解的 ADC 连接剂,可用于合成抗体偶联药物。 | |||
T37575 |
GLcNAc1-b-PNP
|
Others | Others |
GLcNAc1-b-PNP 是N-乙酰基-β-氨基葡萄糖酶的发色底物,可用于量化人血清和尿液中N-乙酰基-β-D-氨基葡萄糖酶的活性。 | |||
T18318 | MC-Val-Ala-PAB-PNP | Others | Others |
MC-Val-Ala-PAB-PNP 是一种用于合成抗体偶联药物的 linker,可降解。 | |||
T17692 |
Boc-Val-Cit-PAB-PNP
|
Others | Others |
Boc-Val-Cit-PAB-PNP 是一种可切割的 ADC 接头,用于合成抗体-药物偶联物。 | |||
T41083 |
pNP-ADPr
pNP-ADPr,ADP-ribose-pNP |
||
pNP-ADPr is a colorimetric substrate employed in the first continuous activity assays for Poly(ADP-ribose) glycohydrolase (PARG) and ADP-ribosyl hydrolase 3 (ARH3). Its utilization facilitates research on poly(ADP-ribose) polymerase (PARP) enzymes. | |||
T78401 |
pNP-ADPr disodium
ADP-ribose-pNP disodium |
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pNP-ADPr 二钠是一种用于检测Poly(ADP-ribose) glycohydrolase (PARG)和ADP-ribosyl hydrolase 3 (ARH3)活性的比色底物。它也适用于poly(ADP-ribose)polymerase (PARP)酶相关研究。 | |||
T3503 |
MC-Val-Cit-PABC-PNP
Maleimidocaproyl-L-valine-L-citrulline-p-aminobenzyl alcohol p-nitrophenyl carbonate,马来酰亚胺基己酰-L-缬氨酸-L-瓜氨酸对氨基苄醇 对硝基苯基碳酸脂 |
Others; AChR | Neuroscience; Others |
MC-Val-Cit-PABC-PNP 是一种组织蛋白酶可裂解的 ADC 肽接头,可用于合成抗体偶联药物。 | |||
T38739 |
Mal-PEG2-Val-Cit-PABA-PNP
Mal-PEG2-Val-Cit-PABA-PNP |
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Mal-PEG2-Val-Cit-PABA-PNP is a cleavable linker compound employed in the synthesis of antibody-drug conjugates (ADCs). | |||
T19139 |
4-Nitrophenyl α-D-galactopyranoside
PNP-alpha-D-Gal,4-硝基苯-α-D-吡喃半乳糖苷,PNP-α-D-Gal |
Others | Others |
4-Nitrophenyl α-D-galactopyranoside (PNP-alpha-D-Gal) 是 4-硝基苯基 (pNP) 糖吡喃糖苷的人工底物,可用于 α-半乳糖苷酶活性的检测。它用作底物能够显著增加 pNP 的释放量。 | |||
T39765 |
Mal-PEG1-Val-Cit-PAB-PNP
Mal-PEG1-Val-Cit-PAB-PNP |
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Mal-PEG1-Val-Cit-PAB-PNP is an ADC linker employed in the synthesis of ADCs, enabling cleavage. | |||
T37733 |
AMP-PNP tetralithium
|
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Non-hydrolyzable AMP analog. Kir6 (KATP) channel blocker. Inhibits fast axonal transport and stabilizes the interaction of membranous organelles with microtubules. Brady (1985) A novel brain ATPase with properties expected for the fast axonal transport motor. Nature 317 73 PMID:2412134 |Yount et al (1971) Adenylyl imidodiphosphate, an adenosine triphosphate analog containing a P-N-P linkage. Biochemistry 10 2484 PMID:4326768 |Hehl and Neumcke (1994) KATP channels of mouse skeletal muscle: mechan... | |||
T41022 | β-D-glucuronide-pNP-carbonate | ||
β-D-glucuronide-pNP-carbonate is an ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs). | |||
T38816 |
Fmoc-Val-Ala-PAB-PNP
|
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Fmoc-Val-Ala-PAB-PNP is a cleavable linker employed for the synthesis of antibody-drug conjugates (ADCs). | |||
T18875 |
(Ac)Phe-Lys(Alloc)-PABC-PNP
|
Others | Others |
'(Ac)Phe-Lys(Alloc)-PABC-PNP serves as a valuable cleavable linker in the development of antibody-drug conjugates.' | |||
T18512 |
OPSS-Val-Cit-PAB-PNP
|
Others | Others |
OPSS-Val-Cit-PAB-PNP is a cleavable linker employed in ADC (antibody-drug conjugates) synthesis [1]. | |||
T17690 |
Boc-Val-Ala-PAB-PNP
|
Others | Others |
Boc-Val-Ala-PAB-PNP is an ADC linker employed for the synthesis of antibody-drug conjugates (ADCs)[1]. This cleavable compound efficiently facilitates the attachment of drugs to antibodies, allowing for targeted delivery and release of therapeutic agents within the body, making it an important component in ADC development. | |||
T17816 | DBCO-Val-Cit-PABC-PNP | Others | Others |
DBCO-Val-Cit-PABC-PNP is a cleavable linker for antibody-drug conjugate (ADC) synthesis[1]. | |||
T17945 |
Fmoc-Ala-Ala-Asn-PABC-PNP
|
Others | Others |
Fmoc-Ala-Ala-Asn-PABC-PNP is a peptide cleavable ADC linker[1]. | |||
T15995 |
Mal-PEG4-Val-Cit-PAB-PNP
|
Others | Others |
Mal-PEG4-Val-Cit-PAB-PNP is a cleavable 4-unit polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T17688 |
Boc-Phe-(Alloc)Lys-PAB-PNP
|
Others | Others |
Boc-Phe-(Alloc)Lys-PAB-PNP serves as a cleavable linker in the synthesis of antibody-drug conjugates (ADCs). | |||
T15953 |
Mal-amido-PEG2-Val-Cit-PAB-PNP
|
Others | Others |
Mal-amido-PEG2-Val-Cit-PAB-PNP is a cleavable 2-unit polyethylene glycol (PEG) based ADC linker utilized in the construction of antibody-drug conjugates (ADCs)[1]. | |||
T14436 | Azido-PEG3-Val-Cit-PAB-PNP | Others | Others |
Azido-PEG3-Val-Cit-PAB-PNP is a cleavable 3 unit PEG ADC linker employed for synthesizing antibody-drug conjugates (ADCs)[1]. It also serves as a PEG-based PROTAC linker for the synthesis of PROTACs[2]. | |||
T17726 |
Cbz-Phe-(Alloc)Lys-PAB-PNP
|
Others | Others |
Cbz-Phe-(Alloc)Lys-PAB-PNP serves as a cleavable linker in the design of antibody-drug conjugates (ADC). | |||
T17981 |
Fmoc-Phe-Lys(Boc)-PAB-PNP
|
Others | Others |
Fmoc-Phe-Lys(Boc)-PAB-PNP is a cleavable antibody-drug conjugate (ADC) linker employed in the synthesis of ADCs. | |||
T17980 |
Fmoc-Phe-Lys(Trt)-PAB-PNP
|
Others | Others |
Fmoc-Phe-Lys(Trt)-PAB-PNP is a cleavable linker for antibody-drug conjugate (ADC) synthesis, specifically designed for use in ADC synthesis. | |||
T31835 |
Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB-PNP
|
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Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB-PNP is a peptide reagent for ADC conjugation that possesses a cleavable peptide sequence. The hydrophilic PEG spacer increases solubility in aqueous media. | |||
T17387 |
Aloc-D-Ala-Phe-Lys(Aloc)-PAB-PNP
|
Others | Others |
Aloc-D-Ala-Phe-Lys(Aloc)-PAB-PNP is a cleavable linker utilized in the synthesis of antibody-drug conjugates (ADCs), which are innovative therapeutic agents that combine the targeting ability of antibodies with potent cytotoxic drugs. | |||
T81870 |
Mal-VC-PAB-PNP-CDN-A
|
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Mal-VC-PAB-PNP-CDN-A是一种ADC活性分子与linker偶联物,具有特定的生物化学功能。 | |||
T77868 | Mal-amide-PEG8-Val-Ala-PAB-PNP | ||
Mal-amide-PEG8-Val-Ala-PAB-PNP 是一款可降解的ADC linker,专门用于抗体偶联活性分子(ADC)的合成。 | |||
T77831 | Fmoc-Glu-(Boc)-Val-Cit-PAB-PNP | ||
Fmoc-Glu-(Boc)-Val-Cit-PAB-PNP 是一种ADC linker,具有可降解 (cleavable) 特性,适用于抗体偶联活性分子 (ADC) 的合成。 | |||
T12399 |
Peldesine
BCX 34 |
Nucleoside Antimetabolite/Analog; HIV Protease | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Proteases/Proteasome |
Peldesine (BCX 34) 是一种有效的、竞争性的、可逆的和口服活性的嘌呤核苷磷酸化酶抑制剂。 Peldesine 抑制 T 细胞增殖,IC50 为 800 nM。 Peldesine 可用于皮肤 T 细胞淋巴瘤、牛皮癣和 HIV 感染的研究。 | |||
T67690 |
pNPG-1
4-Nitrophenyl β-D-glucuronide |
Others | Others |
pNPG-1(4-Nitrophenyl β-D-glucuronide) 是一种葡萄糖醛酸单糖衍生物,是β-葡糖苷酶的显色底物。 | |||
T16554 |
PNPP
|
Others | Others |
PNPP 是用于 ELISA 和常规分光光度测定的碱性和酸性磷酸酶的非蛋白质显色底物。 | |||
T19522 |
PNPG
4-硝基苯-Β-D-吡喃葡萄糖苷,4-Nitrophenyl β-D-glucopyranoside |
Others | Others |
PNPG (4-Nitrophenyl β-D-glucopyranoside) 是一种显色的β-D-葡糖苷酶底物,裂解后会产生黄色溶液。 | |||
T38127 |
pNPS-DHA
|
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pNPS-DHA is an arylamide derivative of docosahexaenoyl ethanolamide that has anti-allergic activity.1It inhibits degranulation of RBL-2H3 mast cells (IC50= 15 μM).pNPS-DHA (1,000 mg/kg) inhibits IgE-dependent passive cutaneous anaphylaxis (PCA) in mice. 1.Kim, I.-H., Kanayama, Y., Nishiwaki, H., et al.Structure-activity relationships of fish oil derivatives with anti-allergic activity in vitro and in vivoJ. Med. Chem.62(21)9576-9592(2019) | |||
TP1847 |
GLGPNPCRKKCYKRDFLGR
|
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GLGPNPCRKKCYKRDFLGR is a synthetic peptide. | |||
T67822L |
Ulodesine
BCX4208 |
Endogenous Metabolite | Metabolism |
Ulodesine (BCX4208) 是一种嘌呤核苷磷酸化酶 (PNP) 抑制剂,对 PNP 有抑制作用,IC50 值为 2.293 nM/L。Ulodesine 可用于研究高尿酸血症。 | |||
T15337 |
Forodesine
呋咯地辛,BCX-1777,Immucillin-H |
Others | Others |
Forodesine is a potent human lymphocyte proliferation inhibitor. Forodesine is an orally active inhibitor of purine nucleoside phosphorylase (IC50s: 0.48 to 1.57 nM for human, mouse, rat, monkey, and dog PNP). It could induce apoptosis in leukemic cells b | |||
T9727 |
2'-Fluoro-2'-Deoxyadenosine
|
Nucleoside Antimetabolite/Analog | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
2′-Deoxy-2′-fluoroadenosine 可用于合成2 ' -脱氧-2 ' -氟修饰的寡核苷酸。它能被大肠杆菌嘌呤核苷磷酸化酶(PNP)有效地分解成毒性物 2-氟腺嘌呤,对表达大肠杆菌 PNP 的肿瘤表现出良好的体内活性。 | |||
T14964 |
CI 972 anhydrous
CI 972 (anhydrous) |
Others | Others |
CI 972 anhydrous is an inhibitor of purine nucleoside phosphorylase (PNP) (Ki: 0.83 μM) used as a T cell-selective immunosuppressive agent. | |||
T11313 |
Forodesine hydrochloride
BCX-1777 hydrochloride,Immucillin-H hydrochloride |
Others | Others |
Forodesine hydrochloride (BCX-1777 hydrochloride), a potent inhibitor of human lymphocyte proliferation, effectively induces apoptosis in leukemic cells by elevating dGTP levels. This compound is an orally active, highly potent purine nucleoside phosphorylase (PNP) inhibitor, demonstrating IC50 values between 0.48 to 1.57 nM across human, mouse, rat, monkey, and dog PNP. | |||
T78379 |
9-Deazaguanine
|
Others | Others |
9-Deazaguanine,一种核苷类似物,有效抑制嘌呤核苷磷酸化酶(PNP)。 | |||
T60799 |
Peldesine dihydrochloride
|
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Peldesine (BCX 34) dihydrochloride 是一种有效的,竞争性,可逆和口服活性的嘌呤核苷磷酸化酶 (PNP) 抑制剂,对人,大鼠和小鼠红细胞 (RBC)PNP 的 IC50分别为 36 nM,5 nM 和 32 nM。Peldesine dihydrochloride 还是一种 T 细胞 (T-cell) 增殖抑制剂,IC50为 800 nM。Peldesine dihydrochloride 可用于皮肤 T 细胞淋巴瘤,牛皮癣和 HIV 感染的研究。 | |||
T73745 |
Ethylidene-4-nitrophenyl-a-D-Maltoheptaoside
|
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Ethylidene-4-nitrophenyl-a-D-Maltoheptaoside (EPS; pNP-G7) 作为α-淀粉酶的底物,主要应用于测定α-淀粉酶的活性。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8083 |
Pyridoxal 5'-phosphate monohydrate
Pyridoxal phosphate monohydrate,Pyridoxal 5-phosphate monohydrate,5-磷酸吡哆醛 |
Others | Others |
Pyridoxal 5'-phosphate monohydrate 是维生素 B6的活性形式,也是多种酶的重要辅因子。它是维生素 B6 在细胞内磷酸化过程中重要的辅酶变异体,能够与其他变异体(如 PNP 、 PMP)发生互换。 | |||
T1709 |
2'-Deoxyinosine
Guanine deoxyriboside,Deoxyinosine,2'-脱氧肌苷 |
Others; Endogenous Metabolite | Metabolism; Others |
2'-Deoxyinosine (Guanine deoxyriboside) 具有 抑制人癌细胞株生长的活性,并发现其与嘌呤核苷磷酸化酶缺乏有关。 |