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T18312Mc-MMAE；马来酰亚胺基己酰-单甲基澳瑞他汀 EMaleimidocaproyl-monomethylauristatin E；Maleimidocaproyl-monomethylaurista
Mc-MMAE (Maleimidocaproyl-monomethylauristatin E) is a drug-linker conjugate for ADC. Mc-MMAE is a maleimidocaproyl-conjugated monomethyl auristatin E, which is a potent tubulin inhibitor.
价 格：￥电议型 号：T18312产 地：中国大陆
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T18311Mc-MMAD；化合物 T18311Mc-MMAD
Mc-MMAD, a drug-linker conjugate for antibody-drug conjugates (ADCs), incorporates the protective group maleimidocaproyl (Mc) conjugated to monomethyl auristatin D (MMAD), a potent inhibitor of tubulin.
价 格：￥电议型 号：T18311产 地：中国大陆
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T18310AZ1508；化合物 T18310MC-Lys-MMETA；MC-Lys-MMETA
AZ1508, a tubulin inhibitor[1], serves as a drug-linker conjugate for antibody-drug conjugates (ADC) targeting breast and stomach cancer treatment.
价 格：￥电议型 号：T18310产 地：中国大陆
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T18309Mc-Leu-Gly-Arg；化合物 T18309Mc-Leu-Gly-Arg
Mc-Leu-Gly-Arg is a cleavable ether linker for antibody-drug conjugates (ADC) design.
价 格：￥电议型 号：T18309产 地：中国大陆
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T18308MC-Gly-Gly-Phe；化合物MC-Gly-Gly-PheMC-Gly-Gly-Phe
MC-Gly-Gly-Phe is a cleavable linker. MC-Gly-Gly-Phe can be used for antibody-drug conjugates (ADC).
价 格：￥电议型 号：T18308产 地：中国大陆
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T18307MC(C5)-Val-Cit；化合物 T18307MC(C5)-Val-Cit
MC(C5)-Val-Cit is a cleavable ADC linker employed in ADCs synthesis [1].
价 格：￥电议型 号：T18307产 地：中国大陆
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T18306MC-Alkyl-Hydrazine Modified MMAF；化合物 T18306MC-Alkyl-Hydrazine Modified MMAF
MC-Alkyl-Hydrazine Modified MMAF is a potent antitumor drug-linker conjugate for ADC, incorporating Modified MMAF, a tubulin inhibitor, through a noncleavable MC-Alkyl-Hydrazine linkage[1].
价 格：￥电议型 号：T18306产 地：中国大陆
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T1815Dapivirine；达匹维林R147681|||TMC120；R147681|||达匹维林|||TMC120
Dapivirine (R147681) is a diarylpyrimidine non-nucleoside reverse transcriptase inhibitor.
价 格：￥电议型 号：T1815产 地：中国大陆
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T17985Gemcitabine-O-Si(di-iso)-O-Mc；化合物 T17985Gemcitabine-O-Si(di-iso)-O-Mc
Gemcitabine-O-Si(di-iso)-O-Mc, a drug-linker conjugate for Antibody-Drug Conjugates (ADC), exhibits potent antitumor activity. It incorporates Gemcitabine, a pyrimidine nucleoside analog antimetabolite and antineoplastic agent, connected through the ADC linker[1].
价 格：￥电议型 号：T17985产 地：中国大陆
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T17833DM4-SMCC；化合物 T17833DM4-SMCC
DM4-SMCC, a non-cleavable drug-linker conjugate for antibody-drug conjugates (ADC), leverages the antitumor efficacy of DM4 (an antitubulin agent) through attachment with the SMCC linker, exhibiting antitumor activity[1].
价 格：￥电议型 号：T17833产 地：中国大陆
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T17741Cys-mcMMAD；化合物 T17741Cys-mcMMAD
Cys-mcMMAD is a drug-linker conjugate for ADC. MMAD is a potent tubulin inhibitor.
价 格：￥电议型 号：T17741产 地：中国大陆
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T17162Triamcinolone hexacetonide；己曲安奈德Triamcinolone hexacetonide
Triamcinolone hexacetonide is used long-acting steroids in the treatment of subacute and chronic inflammatory joint diseases.
价 格：￥电议型 号：T17162产 地：中国大陆
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T17107TMC353121；化合物 T17107TMC353121
TMC353121 is an effective inhibitor of respiratory syncytial virus fusion (pEC50: 9.9).
价 格：￥电议型 号：T17107产 地：中国大陆
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T17106TMC310911；化合物 T17106TMC310911
TMC310911 is an effective and orally active HIV type-1 protease inhibitor (EC50: ranged from 2.2 nM to 14.2 nM for wild-type HIV-1). TMC310911 has effective activity against a wide spectrum of recombinant HIV-1 isolates.
价 格：￥电议型 号：T17106产 地：中国大陆
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T16899SMCC-DM1；化合物SMCC-DM1DM1-SMCC；DM1-SMCC
SMCC-DM1 (DM1-SMCC) (DM1-SMCC) is a drug-linker conjugate which composed of a potent microtubule-disrupting agent DM1 and a linker SMCC to make antibody-drug conjugate (ADC).
价 格：￥电议型 号：T16899产 地：中国大陆
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T16762RMC-4550；化合物RMC-4550RMC-4550
RMC-4550 is an effective and allosteric inhibitor of SHP2 (IC50: 0.583 nM).
价 格：￥电议型 号：T16762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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T16031McMMAF；化合物McMMAFMaleimidocaproyl monomethylauristatin F；Maleimidocaproyl monomethylauristatin F
McMMAF is a protective group-conjugated MMAF. MMAF is a potent tubulin polymerization inhibitor.It is a MMAF derivative having a Maleimidocaproyl linker (MC linker), which is ready to conjugate to antibody or other proteins or biopolymers. Mafodotin is a useful agent for make antibody drug conjugate (ADC) for targeted drug delivery.
价 格：￥电议型 号：T16031产 地：中国大陆
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T16030Mcl1-IN-8；化合物 T16030Mcl1-IN-8
Mcl1-IN-8 is an Mcl-1-PUMA interface inhibitor (Ki: 0.3 μM). In cancer cells, Mcl1-IN-8 shows dual activity on reducing PUMA-dependent apoptosis while deactivating Mcl-1-mediated anti-apoptosis.
价 格：￥电议型 号：T16030产 地：中国大陆
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T16029Mcl1-IN-3；化合物 T16029Mcl1-IN-3
Mcl1-IN-3 is an Mcl1 inhibitor. It has an IC50 and Ki of 0.67 and 0.13 μM, respectively.
价 格：￥电议型 号：T16029产 地：中国大陆
