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T1438Butoconazole nitrate；硝酸布康唑RS 35887；RS 35887|||硝酸布康唑
Butoconazole Nitrate is the nitrate salt form of butoconazole, a synthetic imidazole derivative with fungistatic properties. Butoconazole nitrate (RS 35887) interferes with steroid biosynthesis by inhibiting the conversion of lanosterol to ergosterol, thereby changing the fungal cell membrane lipid composition. This alters cell permeability and leads to growth inhibition. Butoconazole nitrate is active against many dermatophytes and yeasts. It also contains antibacterial effects against some gra
价 格：￥电议型 号：T1438产 地：中国大陆
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T14378LAZD5582 acetate (1258392-53-8 free base)；化合物AZD5582 acetateAZD5582 acetate (1258392-53-8 free base)
AZD5582 acetate is an inhibitor of IAPs, which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. AZD5582 induces apoptosis.
价 格：￥电议型 号：T14378L产 地：中国大陆
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T14378AZD5582；化合物AZD5582AZD5582
AZD5582 is an inhibitor of IAPs, which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. It induces apoptosis.
价 格：￥电议型 号：T14378产 地：中国大陆
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T14360AX-15836；化合物AX-15836AX-15836
AX-15836 is an inhibitor of ERK5 (IC50 : 8 nM).
价 格：￥电议型 号：T14360产 地：中国大陆
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T14358Avoralstat；AVORALSTATBCX4161；BCX4161
Avoralstat (BCX4161) is an oral plasma kallikrein (PKK) inhibitor. Which is used for the treatment of hereditary angioedema.
价 格：￥电议型 号：T14358产 地：中国大陆
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T14324Artemisone；青蒿酮BAY 44-9585|||Artemifone；BAY 44-9585|||Artemifone|||青蒿酮
Artemisone (BAY 44-9585) is a potent and semi-synthetic antimalarial, inhibits P. falciparum strains (IC50: 0.83 nM). It also is a potent inhibitor of human CMV.
价 格：￥电议型 号：T14324产 地：中国大陆
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T14316AR-C155858；化合物AR-C155858AR-C155858
AR-C155858 is an inhibitor of monocarboxylate transporter MCT1 and MCT2 (Kis: 2.3 nM and 10 nM).
价 格：￥电议型 号：T14316产 地：中国大陆
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T14258Aminoethyl-SS-propionic acid；化合物 T14258Aminoethyl-SS-propionic acid
Aminoethyl-SS-propionic acid is an ADC linker compound employed in ADC synthesis [1]. It functions as a cleavable linker in the conjugation of antibodies with drugs, allowing for targeted drug delivery.
价 格：￥电议型 号：T14258产 地：中国大陆
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T14218Amicarbazone；胺唑草酮BAY314666|||BAY-MKH 3586；BAY314666|||胺唑草酮|||BAY-MKH 3586
Amicarbazone (BAY-MKH3586; BAY314666) is a potent PSII inhibitor, disrupting photosynthetic electron transport by binding to the Qb domain of photosystem II. This broad-spectrum herbicide is effective through foliar and root application, showcasing rapid absorption and translocation. However, its effectiveness can be compromised by common PSII inhibitor resistance. With an IC50 value indicating high potency, amicarbazone leads to chlorosis, stunted growth, tissue necrosis, and death in sensitive
价 格：￥电议型 号：T14218产 地：中国大陆
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T14158Ald-CH2-PEG3-CH2-Boc；化合物 T14158Ald-CH2-PEG3-CH2-Boc
Ald-CH2-PEG3-CH2-Boc, a PEG- and Alkyl/ether-based PROTAC linker, is utilized for the synthesis of SGK3 kinase PROTAC degrader[1].
价 格：￥电议型 号：T14158产 地：中国大陆
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T14115Acoziborole；化合物 T14115SCYX-7158|||AN5568；SCYX-7158|||AN5568
Acoziborole (SCYX-7158), a derivative of benzoxaborole, is a safe, effective and structurally novel antigen-worm agent for human African trypanosomiasis (HAT) studies. The MIC value of Acoziborole for T. b. brucei S427 was 0.6 ?g/mL.
价 格：￥电议型 号：T14115产 地：中国大陆
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T14092AC260584；化合物 T14092AC260584
AC260584 is an M1 muscarinic receptor allosteric agonist (pEC50: 7.6).
价 格：￥电议型 号：T14092产 地：中国大陆
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T14071A-385358；化合物A-385358A-385358
A-385358 is a selective Bcl-xL inhibitor with Kis of 0.80 nM for Bcl-xL and 67 nM for Bcl-2, respectively.
价 格：￥电议型 号：T14071产 地：中国大陆
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T140586-FITC6-异硫氰酸荧光素6-异硫氰酸荧光素|||6-Fluorescein Isothiocyanate
6-Fluorescein Isothiocyanate (6-FITC) is a fluorescein derivative widely employed in applications such as flow cytometry.
价 格：￥电议型 号：T14058产 地：中国大陆
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T13974ZL0580；化合物ZL0580ZL0580
ZL0580 induces HIV suppression by inhibiting Tat transactivation and transcription elongation as well as by inducing repressive chromatin structure at the HIV promoter.
价 格：￥电议型 号：T13974产 地：中国大陆
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T13958VHL Ligand 8；化合物 T13958VHL Ligand 8
VHL Ligand 8, a VHL ligand essential for synthesizing ARD-266, acts as a highly potent VHL E3 ligase-based androgen receptor (AR) PROTAC degrader. It efficiently facilitates the degradation of AR protein in AR-positive prostate cancer cell lines LNCaP, VCaP, and 22Rv1, exhibiting DC50 values ranging from 0.2-1 nM [1].
价 格：￥电议型 号：T13958产 地：中国大陆
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T1388Fluconazole；氟康唑UK-49858；氟康唑|||UK-49858
Fluconazole (UK-49858) is a triazole antifungal agent that is used to treat oropharyngeal candidiasis and cryptococcal meningitis in AIDS.
价 格：￥电议型 号：T1388产 地：中国大陆
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T13878(S,S)-Valifenalate化合物 T13878(S,S)-IR5885|||(S,S)-Valiphenal
(S,S)-Valifenalate is an acylamino acid fungicide and is used to control a wide range of fungi belonging to the class of Oomycetes.
价 格：￥电议型 号：T13878产 地：中国大陆
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T13858RA190；化合物RA190RA190
RA190 inhibits proteasome function by covalently binding to cysteine 88 of ubiquitin receptor RPN13.
价 格：￥电议型 号：T13858产 地：中国大陆
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T13824PP58；化合物PP58PP58
PP58 is an inhibitor of PDGFR, FGFR and Src family.
价 格：￥电议型 号：T13824产 地：中国大陆
