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T2056LUNC0064-12 hydrochloride (1430089-64-7(free base))；化合物UNC0064-12 hydrochlorideUNC0064-12 hydrochlori
UNC0064-12 hydrochloride is an inhibitor of VEGFR2.
价 格：￥电议型 号：T2056L产 地：中国大陆
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T20152Tetraconazole；氟醚唑M 14360；M 14360|||氟醚唑
Tetraconazole is an agent of pesticides.
价 格：￥电议型 号：T20152产 地：中国大陆
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T20143L-6424；化合物 T20143L 6424|||Amiodarone related compound G；L 6424|||Amiodarone related compound G
L-6424 is an intermediate of Amiodarone and a non-selective ion channel blocker. It has an antiarrhythmic.
价 格：￥电议型 号：T20143产 地：中国大陆
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T19407Lurasidone Metabolite 14326 D8；化合物 T19407Lurasidone Metabolite 14326 D8
Lurasidone Metabolite 14326 D8 is the deuterium labeled Lurasidone Metabolite 14326.
价 格：￥电议型 号：T19407产 地：中国大陆
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T19251CTX-0294885 hydrochloride (1439934-41-4 free base)；化合物 T19251CTX-0294885 hydrochloride；CTX-0294885 h
CTX-0294885 hydrochloride is an agarose-supported kinase capture reagent.
价 格：￥电议型 号：T19251产 地：中国大陆
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T191434-(6-Bromo-2-benzothiazolyl)benzenamine；化合物 T191434-(6-Bromo-2-benzothiazolyl)benzenamine
4-(6-Bromo-2-benzothiazolyl)benzenamine is a β-amyloid PET tracer and can be used in the diagnosis of neurological diseases.
价 格：￥电议型 号：T19143产 地：中国大陆
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T18143m-PEG12-OH化合物m-PEG12-OHDodecaethylene Glycol Monomethyl Ether
m-PEG12-OH (Dodecaethylene Glycol Monomethyl Ether) is a PEG-based PROTAC linker. m-PEG12-OH can be used in the synthesis of PROTACs. m-PEG12-OH is also a non-cleavable 12 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T18143产 地：中国大陆
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T1730NPS-2143；化合物NPS 2143SB262470|||NPS 2143|||SB 262470A；SB262470|||NPS 2143|||SB 262470A|||2-氯-6-[(2R)-
NPS-2143 (SB 262470A) is a novel potent and selective antagonist of Ca(2+) receptor.
价 格：￥电议型 号：T1730产 地：中国大陆
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T17143Toyocamycin；丰加霉素Vengicide；丰加霉素|||Vengicide
Toyocamycin (Vengicide) is an adenosine analog produced by Actinomycete, acts as an XBP1 inhibitor, inhibits IRE1α-induced ATP-dependent XBP1 mRNA cleavage (IC50: 80 nM). Toyocamycin induces apoptosis.
价 格：￥电议型 号：T17143产 地：中国大陆
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T16143MRTX-1257；化合物MRTX-1257MRTX-1257
MRTX-1257 is a selective, irreversible, and covalent inhibitor of KRAS G12C. It has an IC50 of 900 pM for KRAS dependent ERK phosphorylation in H358 cells. MRTX1257 demonstrated 31% bioavailability in the mouse, with free fraction exposures well above the cellular potency In a PK/PD experiment, 77% target engagement.
价 格：￥电议型 号：T16143产 地：中国大陆
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T15623JNJ-61432059；化合物JNJ-61432059JNJ-61432059
JNJ-61432059 is an oral active and selective negative modulator of TARP γ?8 Selective AMPAR(pIC50: 9.7).
价 格：￥电议型 号：T15623产 地：中国大陆
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T15143DMP-543；化合物DMP-543XR-543；XR-543
DMP-543 (XR-543) is a potassium channel (KV7 channel) blocker that enhances the release of neurotransmitters.
价 格：￥电议型 号：T15143产 地：中国大陆
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T1485Methotrexate；甲氨蝶呤NCI-C04671|||WR19039|||Amethopterin|||CL14377；NCI-C04671|||WR19039|||Amethopterin||
Methotrexate (WR19039) is a folate analog, an inhibitor of the dihydrofolate reductase DHFR. Methotrexate has antimetabolic, antitumor, and immunosuppressive activities, and is commonly used in rheumatoid arthritis and various tumors.
价 格：￥电议型 号：T1485产 地：中国大陆
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T14399Azide-PEG7-Tos；化合物 T14399Azide-PEG7-Tos
Azide-PEG7-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：T14399产 地：中国大陆
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T14398Azide-PEG6-Tos；化合物 T14398Azide-PEG6-Tos
Azide-PEG6-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：T14398产 地：中国大陆
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T14397Azide-PEG5-Tos；化合物 T14397Azide-PEG5-Tos
Azide-PEG5-Tos is a cleavable PEG linker consisting of five units, employed for the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T14397产 地：中国大陆
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T14396Azide-PEG5-Boc；化合物 T14396Azide-PEG5-Boc
Azide-PEG5-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：T14396产 地：中国大陆
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T14395Azide-PEG4-Tos；化合物 T14395Azide-PEG4-Tos
Azide-PEG4-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：T14395产 地：中国大陆
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T14394Azide-PEG3-Tos；化合物 T14394Azide-PEG3-Tos
Azide-PEG3-Tos is a PEG-based PROTAC linker utilized in the synthesis of PROTACs[1]. It is a non-cleavable 3 unit PEG ADC linker employed in the synthesis of antibody-drug conjugates (ADCs)[2].
价 格：￥电议型 号：T14394产 地：中国大陆
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T14393Azide-PEG3-C1-Ala；化合物 T14393Azide-PEG3-C1-Ala
Azide-PEG3-C1-Ala 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：T14393产 地：中国大陆
