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T77893Fmoc-Gly-NH-CH2-O-CH2COOH；化合物 Fmoc-Gly-NH-CH2-O-CH2COOHFmoc-Gly-NH-CH2-O-CH2COOH
Fmoc-Gly-NH-CH2-O-CH2COOH is an ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs) [1].
价 格：￥电议型 号：T77893产 地：中国大陆
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T77818Fmoc-Gly-Gly-Phe-OH；化合物 Fmoc-Gly-Gly-Phe-OHFmoc-Gly-Gly-Phe-OH
Fmoc-Gly-Gly-Phe-OH is a cleavable ADC linker utilized in antibody-drug conjugate (ADC) synthesis [1].
价 格：￥电议型 号：T77818产 地：中国大陆
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T77732LHFY-4A HCL (2094810-82-7 Free base)；化合物 HFY-4A HCL (2094810-82-7 Free base)HFY-4A HCL (2094810
HFY-4A HCL is a novel HDAC inhibitor.HFY-4A HCL has antitumour activity and has shown antiproliferative activity in breast cancer cells.
价 格：￥电议型 号：T77732L产 地：中国大陆
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T77732HFY-4A；化合物 HFY-4AHFY-4A
HFY-4A is a novel HDAC inhibitor.HFY-4A has antitumour activity and has shown antiproliferative activity in breast cancer cells.
价 格：￥电议型 号：T77732产 地：中国大陆
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T77692F7H；化合物F7HF7H
F7H is a potent Frizzled receptor FZD7 antagonist with an IC50 value of 1.25 μM.F7H is a potent ligand for the transmembrane structural domain (TMD) of FZD7, with potential antitumor and bacteriostatic activity.
价 格：￥电议型 号：T77692产 地：中国大陆
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T76659Acetyl-PHF5 amide；化合物 Acetyl-PHF5 amideAcetyl-PHF5 amide
Acetyl-PHF5 amide is a tau peptide with amyloidogenic properties. It can undergo polymerization to form filamentous structures [1].
价 格：￥电议型 号：T76659产 地：中国大陆
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T76652PHF6；化合物 PHF6PHF6
PHF6 (VQIVYK), a sequence within the third microtubule-binding repeat region of the tau protein, initiates the aggregation of the full-length tau protein through its self-assembly capabilities [1].
价 格：￥电议型 号：T76652产 地：中国大陆
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T7643Fmoc-Ser(O-α-D-GalNAc(OAc)3)-OH；化合物Fmoc-Ser(O-α-D-GalNAc(OAc)3)-OHFmoc-Ser-(GalNAc(Ac)3-alpha-D)-OH|
Fmoc-Ser(O-α-D-GalNAc(OAc)3)-OH (Fmoc-Ser(Ac3AcNH-α-Gal)-OH) is an anti-tumor drug
价 格：￥电议型 号：T7643产 地：中国大陆
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T76222hFSH-β-(33-53) (TFA)；化合物 hFSH-β-(33-53) (TFA)hFSH-β-(33-53) (TFA)
hFSH-β-(33-53) TFA, a thiol-containing peptide representing the second follicle-stimulating hormone receptor (FSHR) binding domain, acts as an FSHR antagonist. It prevents FSH from binding to its receptor and partially promotes estradiol synthesis in Sertoli cells [1] [2] [3].
价 格：￥电议型 号：T76222产 地：中国大陆
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T75997Acetyl-PHF6 amide TFA；化合物 Acetyl-PHF6 amide TFAAcetyl-PHF6 amide TFA
Acetyl-PHF6 amide TFA (AcPHF6 TFA) is a tau derived hexapeptide.
价 格：￥电议型 号：T75997产 地：中国大陆
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T7593LLevomefolate sodium；化合物 T7593LL 5 MTHF sodium|||L-5-MTHF sodium|||L5MTHF sodium,；L 5 MTHF sodium|||L
Levomefolate calcium is a primary biologically active form of folate used at the cellular level for dna reproduction, the cysteine cycle and the regulation of homocysteine
价 格：￥电议型 号：T7593L产 地：中国大陆
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T74838MTHFD2-IN-4 sodium；化合物 MTHFD2-IN-4 sodiumMTHFD2-IN-4 sodium
MTHFD2-IN-4 sodium, a potent inhibitor of MTHFD2 and a tricyclic coumarin derivative, is applicable in cancer research [1].
价 格：￥电议型 号：T74838产 地：中国大陆
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T74837MTHFD2-IN-4；化合物 MTHFD2-IN-4MTHFD2-IN-4
MTHFD2-IN-4, a tricyclic coumarin derivative, serves as a potent inhibitor of MTHFD2 and has applications in cancer research [1].
价 格：￥电议型 号：T74837产 地：中国大陆
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T74836MTHFD2-IN-3；化合物 MTHFD2-IN-3MTHFD2-IN-3
MTHFD2-IN-3 (compound 10), a potent inhibitor of methylenetetrahydrofolate dehydrogenase (MTHFD2), demonstrates significant efficacy in obstructing the activity of this enzyme [1].
价 格：￥电议型 号：T74836产 地：中国大陆
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T74835MTHFD2-IN-2；化合物 MTHFD2-IN-2MTHFD2-IN-2
MTHFD2-IN-2 (compound 13) serves as a potent inhibitor of methylenetetrahydrofolate dehydrogenase (MTHFD2) [1].
价 格：￥电议型 号：T74835产 地：中国大陆
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T74834MTHFD2-IN-1；化合物 MTHFD2-IN-1MTHFD2-IN-1
MTHFD2-IN-1 (compound 12) is a potent inhibitor of methylenetetrahydrofolate dehydrogenase (MTHFD2) [1].
价 格：￥电议型 号：T74834产 地：中国大陆
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T73328DHFR-IN-5；化合物 DHFR-IN-5DHFR-IN-5
DHFR-IN-5, an orally active and potent inhibitor of dihydrofolate reductase (DHFR), exhibits a K_i value of 0.54 nM against the quadruple mutant Plasmodium falciparum DHFR, demonstrating anti-malarial activity.
价 格：￥电议型 号：T73328产 地：中国大陆
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T71732Fmoc-ε-Acp-OH；化合物 Fmoc-ε-Acp-OHFmoc-ε-Acp-OH
Fmoc-ε-Acp-OH can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applications. Fmoc-ε-Acp-OH is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
价 格：￥电议型 号：T71732产 地：中国大陆
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T7094Levomefolic Acid；5-甲基四氢叶酸5-MTHF；L-5-甲基四氢叶酸|||5-MTHF|||5-甲基四氢叶酸
Levomefolic Acid (5-MTHF) is a natural, active form of folic acid used at the cellular level for DNA reproduction, the cysteine cycle and the regulation of homocysteine among other functions. Levomefolinic acid is used as a treatment and to prevent Folate Deficiency
价 格：￥电议型 号：T7094产 地：中国大陆
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T70638p38-α MAPK-IN-5；化合物 CHF-6297p38-α MAPK-IN-5
P38-α MAPK-IN-5 is a potent inhibitor of p38α, demonstrating inhibitory concentrations (IC50) of 0.1 nM for p38α, 0.2 nM for p38β, 944 nM for p38γ, and 4100 nM for p38δ. It exhibits anti-inflammatory properties and holds potential for research in asthma and chronic obstructive pulmonary disease (COPD).
价 格：￥电议型 号：T70638产 地：中国大陆
