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T80306A8SGLP-1 TFA；化合物 A8SGLP-1 TFAA8SGLP-1 TFA
A8SGLP-1 TFA, an orally active GLP-1 analogue, features a serine substitution for alanine at position 8. This compound effectively lowers blood glucose in db/db mice, maintaining its function [1].
价 格：￥电议型 号：T80306产 地：中国大陆
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T80305A8SGLP-1；化合物 A8SGLP-1A8SGLP-1
A8SGLP-1, an orally active GLP-1 analogue, features serine substituted for alanine at position 8. It effectively reduces blood glucose in db/db mice, maintaining its function [1].
价 格：￥电议型 号：T80305产 地：中国大陆
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T79542SGC-UBD253；化合物 SGC-UBD253SGC-UBD253
SGC-UBD253 is a potent antagonist of the HDAC6-UBD interaction and may be utilized in cancer research [1].
价 格：￥电议型 号：T79542产 地：中国大陆
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T78425GK16S；化合物 GK16SGK16S
GK16S, a UCHL1 chemogenomic probe, serves as a complementary tool to GK13S for the investigation of UCHL1 function in cellular studies [1].
价 格：￥电议型 号：T78425产 地：中国大陆
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T78362Transglutaminase；转谷氨酰胺酶TG；TG
Transglutaminase (TG) is a thiolase that induces intermolecular cross-linking of proteins, by catalysing the formation of isopeptide bonds between the γ-carboxamide group of glutamine residues and the primary ε-amine group of other compounds. The enzyme plays a role in a variety of physiological processes including coagulation, antimicrobial immune responses and photosynthesis.
价 格：￥电议型 号：T78362产 地：中国大陆
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T78026LQVTDSGLYRCVIYHPP TFA；化合物 LQVTDSGLYRCVIYHPP TFALQVTDSGLYRCVIYHPP TFA
LQVTDSGLYRCVIYHPP (LP17) TFA is a TREM-1 (triggering receptor expressed on myeloid cells) inhibitory peptide that notably mitigates ischemic infarction and neuronal damage. This compound is capable of penetrating the brain to inhibit TREM-1 [1].
价 格：￥电议型 号：T78026产 地：中国大陆
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T78025LQVTDSGLYRCVIYHPP；化合物 LQVTDSGLYRCVIYHPPLQVTDSGLYRCVIYHPP
LQVTDSGLYRCVIYHPP (LP17) is a TREM-1 (triggering receptor expressed on myeloid cells) inhibitory peptide that mitigates ischemia-induced infarction and neuronal damage. It can penetrate the brain and inhibit TREM-1 [1].
价 格：￥电议型 号：T78025产 地：中国大陆
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T77813SG3199-Val-Ala-PAB；化合物 SG3199-Val-Ala-PABSG3199-Val-Ala-PAB
SG3199-Val-Ala-PAB is an intermediate in the synthesis of Tesirine, a conjugate of agent-linker for antibody-drug conjugates (ADCs), utilized in the research of various cancers [1].
价 格：￥电议型 号：T77813产 地：中国大陆
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T77362Vorsetuzumab；沃瑟妥珠单抗SGN-70；SGN-70
Vorsetuzumab (Anti-Human CD70 Recombinant Antibody) is a monoclonal antibody targeting the CD70 antibody. Vorsetuzumab has anticancer activity and can enhance the macrophage-associated phagocytosis of kidney cancer cells and inhibit Burkitt lymphoma.
价 格：￥电议型 号：T77362产 地：中国大陆
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T76707Brentuximab vedotin；维布妥昔单抗SGN-35；SGN-35
Brentuximab vedotin (SGN-35) is an antibody-activated molecule coupling (ADC) targeting CD30 with antitumor activity for the study of lymphomas.
价 格：￥电议型 号：T76707产 地：中国大陆
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T76618VPLSLYSG；化合物 VPLSLYSGVPLSLYSG
VPLSLYSG, an octapeptide susceptible to degradation by matrix metalloproteinase-9 (MMP-9), MMP-1, and MMP-2, holds potential applications as an MMP substrate [1] [2] [3].
价 格：￥电议型 号：T76618产 地：中国大陆
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T76312LsGnRH-A acetate；化合物 sGnRH-A acetatesGnRH-A acetate
sGnRH-A acetate, a salmon gonadotropin-releasing hormone (GnRH) analogue, stimulates growth hormone secretion and serves as an ovulation inducer for artificial insemination [1] [2].
价 格：￥电议型 号：T76312L产 地：中国大陆
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T76312sGnRH-A；化合物 sGnRH-AsGnRH-A
sGnRH-A, a salmon gonadotropin-releasing hormone (GnRH) analogue, promotes growth hormone secretion and serves as an ovulation inducer for artificial insemination [1] [2].
价 格：￥电议型 号：T76312产 地：中国大陆
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T76250LVSGLNPSLWSIFGLQFILLWLVSGSRHYLW TFA；化合物 VSGLNPSLWSIFGLQFILLWLVSGSRHYLW TFAVSGLNPSLWSIFGLQFILLWLVSGSRH
VSGLNPSLWSIFGLQFILLWLVSGSRHYLW (TFA), a 30-amino-acid peptide, mimics the C-terminal domain of α2δ-1, known as α2δ-1Tat peptide. This compound disrupts the α2δ-1 - NMDAR interaction both in vitro and in vivo, demonstrating potential utility in neuropathic pain research [1].
价 格：￥电议型 号：T76250L产 地：中国大陆
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T76250VSGLNPSLWSIFGLQFILLWLVSGSRHYLW；化合物 VSGLNPSLWSIFGLQFILLWLVSGSRHYLWVSGLNPSLWSIFGLQFILLWLVSGSRHYLW
VSGLNPSLWSIFGLQFILLWLVSGSRHYLW, a 30-amino-acid peptide, mirrors the C-terminal domain of α2δ-1 and is recognized as the α2δ-1Tat peptide. It disrupts the α2δ-1 - NMDAR interaction both in vitro and in vivo, offering a potential research tool for neuropathic pain studies [1].
价 格：￥电议型 号：T76250产 地：中国大陆
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T76201LEESGGGLVQPGGSMK TFA；化合物 LEESGGGLVQPGGSMK TFALEESGGGLVQPGGSMK TFA
LEESGGGLVQPGGSMK TFA, a proteolysis peptide component of Infliximab, serves for the quantitative analysis of the latter. Infliximab is a chimeric monoclonal IgG1 antibody, binding specifically to TNF-α [1].
价 格：￥电议型 号：T76201产 地：中国大陆
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T76003MSG606 TFA；化合物 MSG606 TFAMSG606 TFA
MSG606 TFA, a potent antagonist of the human MC1 receptor (IC50 = 17 nM), functions as a partial agonist at the human MC3 and MC5 receptors (EC50 values of 59 and 1300 nM, respectively). It demonstrates binding affinity for A375 melanoma cells in vitro and selectively reverses induced hyperalgesia in female mice without affecting male mice.
价 格：￥电议型 号：T76003产 地：中国大陆
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T75860GTFTSDVSKQMEEEAVRLFIEWLKNGGPSSGAPPPS；化合物 GTFTSDVSKQMEEEAVRLFIEWLKNGGPSSGAPPPSGTFTSDVSKQMEEEAVRLFIEWL
GTFTSDVSKQMEEEAVRLFIEWLKNGGPSSGAPPPS is an Exendin-4 peptide derivative.
价 格：￥电议型 号：T75860产 地：中国大陆
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T75859FTSDVSKQMEEEAVRLFIEWLKNGGPSSGAPPPS；化合物 FTSDVSKQMEEEAVRLFIEWLKNGGPSSGAPPPSFTSDVSKQMEEEAVRLFIEWLKNGGPS
FTSDVSKQMEEEAVRLFIEWLKNGGPSSGAPPPS is an Exendin-4 peptide derivative.
价 格：￥电议型 号：T75859产 地：中国大陆
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T75182GK13S；化合物 GK13SGK13S
G13KS is a deubiquitinase UCHL1 ligand and inhibitor. G13KS inhibits recombinant and cellular UCHL1. G13KS reduces levels of monoubiquitin in human glioblastoma cells [1] .
价 格：￥电议型 号：T75182产 地：中国大陆
