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T16646Propargyl-PEG7-Boc；化合物 T16646Propargyl-PEG7-Boc
Propargyl-PEG7-Boc is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T16646产 地：中国大陆
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T16493PF-06465469；化合物 T16493PF-06465469
PF-06465469 is a covalent ITK inhibitor(IC50: 2 nM).
价 格：￥电议型 号：T16493产 地：中国大陆
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T16469Pentetreotide；化合物 T16469Pentetreotide
Pentetreotide is an indium-labeled somatostatin analog and can be used for nuclear medicine imaging. Pentetreotide is a diethylenetriaminopentaacetic conjugate of Octreotide. Somatostatin receptor scintigraphy with Pentetreotide is effective in visualizing neuroendocrine tumors, and its metastasis.
价 格：￥电议型 号：T16469产 地：中国大陆
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T16468Pentaethylene glycol；化合物 T16468Pentaethylene glycol
Pentaethylene glycol is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T16468产 地：中国大陆
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T16467Pentaethylene glycol monomethyl ether；化合物 T16467Pentaethylene glycol monomethyl ether
Pentaethylene glycol monomethyl ether (PEG-MME) is a PEG-based PROTAC linker, which is employed for the synthesis of PROTACs[1].
价 格：￥电议型 号：T16467产 地：中国大陆
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T16466Penicillin G Procaine化合物 T16466PGP
Penicillin G Procaine is a β-lactam antibiotic and is a crystalline complex produced by chemically combining penicillin G with procaine.
价 格：￥电议型 号：T16466产 地：中国大陆
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T16465Penicillin G benzathine苄星青霉素Benzathine benzylpenicillin|||Benzathine penicilline G
Penicillin G benzathine has anti-bacterial infectious activity and can be used to study early syphilis.
价 格：￥电议型 号：T16465产 地：中国大陆
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T16464Pelubiprofen；化合物 T16464Pelubiprofen
Pelubiprofen, an orally active non-steroidal anti-inflammatory drug (NSAID) belonging to the 2-arylpropionic acid family, selectively inhibits COX-2 activity alongside COX activity and the transforming growth factor-β activated kinase 1-IκB kinase β-NF-κB pathway. It demonstrates significant anti-inflammatory and analgesic effects.
价 格：￥电议型 号：T16464产 地：中国大陆
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T16463PEG8-Tos；化合物 T16463PEG8-Tos
PEG8-Tos is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T16463产 地：中国大陆
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T16462PEG5-Tos；化合物 T16462PEG5-Tos
PEG5-Tos is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T16462产 地：中国大陆
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T16460PEG4-sulfonic acid；化合物 T16460PEG4-sulfonic acid
PEG4-sulfonic acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T16460产 地：中国大陆
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T1646Famciclovir；泛昔洛韦BRL 42810；泛昔洛韦|||BRL 42810
Famciclovir (BRL 42810) is a Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor. The mechanism of action of famciclovir is as a DNA Polymerase Inhibitor, and DNA Polymerase Inhibitor.
价 格：￥电议型 号：T1646产 地：中国大陆
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T15826Lometrexol；洛美曲索LY 264618|||DDATHF；LY 264618|||DDATHF
Lometrexol (LY 264618), an antipurine Antifolate, can inhibit the activity of glycinamide ribonucleotide formyltransferase (GARFT) but do not induce detectable levels of DNA strand breaks. Lometrexol can further inhibit de novo purine synthesis, causing abnormal cell proliferation and Apoptosis, even cell cycle arrest. Lometrexol has anticancer activity. Lometrexol also is a potent human Serine hydroxymethyltransferase1/2 (hSHMT1/2) inhibitor.
价 格：￥电议型 号：T15826产 地：中国大陆
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T15646KBU2046；化合物KBU2046KBU2046
KBU2046 is an orally administered compound that inhibits cell motility and invasion, effectively suppressing cancer metastasis and extending lifespan. This compound uniquely targets and binds to chaperone heterocomplexes, selectively modifying the interaction of client proteins involved in motility regulation, while avoiding the characteristics typical of classical HSP90 inhibitors.
价 格：￥电议型 号：T15646产 地：中国大陆
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T15624JNJ-64619178；化合物JNJ-64619178JNJ-64619178
JNJ-64619178 is a selective, orally active, and pseudo-irreversible inhibitor of protein arginine methyltransferase 5 (IC50: 0.14 nM). It has effective activity In lung cancer.
价 格：￥电议型 号：T15624产 地：中国大陆
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T15404GNE-6468；化合物 T15404GNE-6468
GNE-6468 is a potent and selective agonist of RORγ(RORc) (EC50: 13 nM for HEK-293 cell).
价 格：￥电议型 号：T15404产 地：中国大陆
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T14646Bis-PEG6-NHS ester；化合物 T14646Bis-PEG6-NHS ester
Bis-PEG6-NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T14646产 地：中国大陆
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T13646Desisobutyryl-ciclesonide化合物 T13646CIC-AP|||Ciclesonide active principle
Desisobutyryl-ciclesonide has an affinity for glucocorticoid receptors. Desisobutyryl-ciclesonide is the active metabolite of Ciclesonide.
价 格：￥电议型 号：T13646产 地：中国大陆
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T131719Compound TBBP06469；化合物 TBBP06469Compound TBBP06469
Compound TBBP06469 is a useful organic compound for research related to life sciences. The catalog number is T131719 and the CAS number is 3682-03-9.
价 格：￥电议型 号：T131719产 地：中国大陆
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T131646Compound 0449-0136；化合物 0449-0136Compound 0449-0136
Compound 0449-0136 is a useful organic compound for research related to life sciences and the catalog number is T131646.
价 格：￥电议型 号：T131646产 地：中国大陆
