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T80993Thioacetamide-S-oxide；化合物 Thioacetamide-S-oxideThioacetamide-S-oxide
Thioacetamide-S-oxide, a metabolite of Thiocetamide, functions as a δ-aminolevulinic acid (ALA) synthetase inhibitor [1].
价 格：￥电议型 号：T80993产 地：中国大陆
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T79164-Acetamidobenzenesulfonyl azide；4-乙酰氨基苯磺酰叠氮4-Acetamidobenzenesulfonyl azide
4-Acetamidobenzenesulfonyl azide is used in a variety of scientific research applications, including the synthesis of drugs, peptides and other biologically active molecules. It is also used as a catalyst in polymerization reactions and polymer synthesis.
价 格：￥电议型 号：T7916产 地：中国大陆
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T7863Hexamethylene bisacetamide；N,N’-六亚甲基双乙酰胺Hexamethylene bisacetamide
Hexamethylene bisacetamide inhibits BET Bromodomain Proteins.
价 格：￥电议型 号：T7863产 地：中国大陆
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T782302,4′-Dichloroacetanilide；2,4′-二氯乙酰苯胺2-chloro-N-(4-chlorophenyl)acetamide；2-chloro-N-(4-chlorophenyl)
2,4′-Dichloroacetanilide (2-chloro-N-(4-chlorophenyl)acetamide) has antifungal activity and inhibits T. asteroides with a minimum inhibitory concentration (MIC) of 6.25 μg/mL.
价 格：￥电议型 号：T78230产 地：中国大陆
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T77885(Aminooxy)acetamide-Val-Cit-PAB-MMAE；化合物 (Aminooxy)acetamide-Val-Cit-PAB-MMAE(Aminooxy)acetamide-Val
(Aminooxy)acetamide-Val-Cit-PAB-MMAE (MMAE 5) serves as an intermediate for synthesizing drug-linker conjugates in antibody-drug conjugates (ADCs). This compound is first conjugated to a polyamide through oxime bond formation, resulting in an MMAE polyamide conjugate. Subsequently, the MMAE polyamide conjugate is attached to Trastuzumab to create the ADC [1].
价 格：￥电议型 号：T77885产 地：中国大陆
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T77878Desthiobiotin-Iodoacetamide；化合物 Desthiobiotin-IodoacetamideDesthiobiotin-Iodoacetamide
Desthiobiotin-Iodoacetamide serves as an ADC (Antibody-Drug Conjugate) Linker and functions as a probe for labeling cell lysis in Oridonin-treated cells [1].
价 格：￥电议型 号：T77878产 地：中国大陆
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T77817Lys(MMT)-PAB-oxydiacetamide-PEG8-N3；化合物 Lys(MMT)-PAB-oxydiacetamide-PEG8-N3Lys(MMT)-PAB-oxydiacetami
Lys(MMT)-PAB-oxydiacetamide-PEG8-N3 is a cleavable linker for antibody-drug conjugate (ADC) synthesis that facilitates the attachment of therapeutic agents to antibodies [1].
价 格：￥电议型 号：T77817产 地：中国大陆
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T77639Pyridine-4-Acetamide；吡啶-4-乙酰胺4-Pyridineacetamide；4-Pyridineacetamide
Pyridine-4-Acetamide (4-Pyridineacetamide) is a pyridine-based ligand involved in the synthesis of W6S8 clusters.
价 格：￥电议型 号：T77639产 地：中国大陆
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T77597SXC 2023；化合物SXC 2023(S)-2-acetamido-3-(4-methylbenzoylthio)propanoic acid；(S)-2-acetamido-3-(4-methy
SXC 2023 ((S)-2-acetamido-3-(4-methylbenzoylthio)propanoic acid) is a therapeutic prodrug of N-acetyl-L-cysteine for the treatment of CNS disorders and neurocognitive disorders, and can be used to treat glutamatergic dysfunction and psychiatric disorders in which oxidative stress plays a key role.
价 格：￥电议型 号：T77597产 地：中国大陆
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T76902-hydroxy Flutamide；羟基氟他胺2-hydroxy Flutamide
2-hydroxy Flutamide is competitive inhibition of androgen receptor (AR) for the treatment of prostate cancer
价 格：￥电议型 号：T7690产 地：中国大陆
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T7642Cilostamide；OPC 3689 西洛酰胺OPC3689；OPC3689|||OPC 3689 西洛酰胺
Cilostamide (OPC3689) is a selective phosphodiesterase (PDE)3A and PDE3B inhibitor(IC50 values of 27 and 50 nM, respectively)
价 格：￥电议型 号：T7642产 地：中国大陆
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T75129Luxdegalutamide；化合物LuxdegalutamideARV-766；ARV-766
Luxdegalutamide (ARV-766) is an orally available and effective protein degrader of protein hydrolysis-targeted chimeras (PROTAC).Luxdegalutamide degrades the wild-type androgen receptor AR, as well as AR LBD mutants including those associated with the most prevalent pathogenic AR L702H, H875Y and T878A mutations.
价 格：￥电议型 号：T75129产 地：中国大陆
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T75083Faznolutamide；化合物 FaznolutamideFaznolutamide
Faznolutamide is an antiandrogen agent [1] [2] .
价 格：￥电议型 号：T75083产 地：中国大陆
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T7445Acetamide乙酰胺ethanamide|||乙酰胺|||Acetic acid amide
Acetamide (ethanamide) is found in red beetroot,is used primarily as a solvent and a plasticizer.
价 格：￥电议型 号：T7445产 地：中国大陆
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T72955Gumelutamide；化合物 GumelutamideGumelutamide
Gumelutamide, a tetrahydropyridopyrimidine compound, functions as both an antiandrogen and an antineoplastic agent by acting as an androgen antagonist.
价 格：￥电议型 号：T72955产 地：中国大陆
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T72382-Acetamidophenol；化合物 2-AcetamidophenolOrthocetamol；Orthocetamol
2-Acetamidophenol (Orthocetamol) has analgesic and antipyretic effects. 2-Acetamidophenol is an isomer of Paracetamol (4-acetamidophenol).
价 格：￥电议型 号：T7238产 地：中国大陆
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T71441Glutathione palmitamide；化合物 Glutathione palmitamideGlutathione palmitamide
Glutathione palmitamide is a hydrophilic derivative of the protein tyrosine phosphatase inhibitor phenylarsine oxide (PAO). It inhibits angiogenesis and tumour growth.
价 格：￥电议型 号：T71441产 地：中国大陆
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T69758Flutamide-d7；化合物 Flutamide-d7Flutamide-d7
Flutamide-d7 is intended for use as an internal standard for the quantification of flutamide by GC- or LC-MS. Flutamide is an androgen receptor antagonist and prodrug form of 2-hydroxy flutamide. Flutamide is converted to 2-hydroxy flutamide by the cytochrome P450 (CYP) isoform CYP1A2 in human liver microsomes. It is cytotoxic to PC3 and LNCaP prostate cancer cells with IC50 values of 98.8 and 81.8 ?M, respectively. Flutamide (50 mg/kg per day) reduces tumor growth in a PC-82 mouse xenograft mo
价 格：￥电议型 号：T69758产 地：中国大陆
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T6915Darolutamide；化合物DarolutamideODM-201|||BAY-1841788；ODM-201|||BAY-1841788
Darolutamide (BAY-1841788) is an androgen receptor (AR) antagonist that blocks AR nuclear translocation (Ki: 11 nM).
价 格：￥电议型 号：T6915产 地：中国大陆
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T68942Caricotamide；化合物 CaricotamideCaricotamide
Caricotamide is a synthetic co-substrate that activates the human endogenous enzyme NRH:quinone oxidoreductase 2 (NQO2) with potential chemoadjuvant activity. When caricotamide is administered simultaneously with the prodrug tretazicar, NQO2 converts tretazicar to the bifunctional alkylating agent dinitrobenzamide, which is capable of forming a high degree of DNA interstrand cross-links, resulting in the inhibition of DNA replication and the induction of apoptosis. NQO2 has been found to be over
价 格：￥电议型 号：T68942产 地：中国大陆
