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T77511TRPA1-IN-2；化合物TRPA1-IN-2TRPA1-IN-2
TRPA1-IN-2 is a potent and orally active TRPA1 inhibitor with an IC50 value of 0.04 ?M.TRPA1-IN-2 has anti-inflammatory activity.
价 格：￥电议型 号：T77511产 地：中国大陆
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T7723Carumonam Sodium；化合物 T7723Ro172301|||Ro-17-2301|||AMA1080|||AMA-1080|||Ro 17 2301|||AMA 1080；Ro17230
Carumonam Sodium is a monobactam, penicillin-binding protein inhibitor. It is used as antibacterials.
价 格：￥电议型 号：T7723产 地：中国大陆
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T76673Bemarituzumab；贝玛妥珠单抗FPA144；FPA144
Bemarituzumab is a novel humanized IgG1 monoclonal antibody targeting FGFR2b. Bemarituzumab prevents FGFR2b from binding to FGF and activation. Potential applications of Bemarituzumab in cancer research.
价 格：￥电议型 号：T76673产 地：中国大陆
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T7649Tyrphostin A1；(4-甲氧基苄烯)丙二腈AG9|||Tyrphostin 1；AG9|||(4-甲氧基苄烯)丙二腈|||Tyrphostin 1
Tyrphostin A1 (Tyrphostin 1) is an inhibitor of EGFR tyrosine kinase .
价 格：￥电议型 号：T7649产 地：中国大陆
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T75949NoxA1ds TFA；化合物 NoxA1ds TFANoxA1ds TFA
NoxA1ds TFA is a potent and selective inhibitor of NADPH oxidase 1 (NOX1), with an inhibition concentration (IC50) of 20 nM, demonstrating selectivity over NOX2, NOX4, NOX5, and xanthine oxidase. It effectively inhibits NOX1-derived O2- production in HT-29 human colon cancer cells and attenuates VEGF-induced migration of human pulmonary artery endothelial cells under hypoxic conditions in vitro.
价 格：￥电议型 号：T75949产 地：中国大陆
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T75921[Ala11,D-Leu15]-Orexin B(human) TFA；化合物 [Ala11,D-Leu15]-Orexin B(human) TFA[Ala11,D-Leu15]-Orexin B(
[Ala11,D-Leu15]-Orexin B(human) TFA is a potent, selective agonist for the orexin-2 receptor (OX2), demonstrating 400-fold higher selectivity for OX2 (EC 50 =0.13 nM) compared to the orexin-1 receptor (OX1) with an EC 50 of 52 nM.
价 格：￥电议型 号：T75921产 地：中国大陆
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T75887[Ala113]MBP(104-118) TFA；化合物 [Ala113]MBP(104-118) TFA[Ala113]MBP(104-118) TFA
[Ala113]MBP(104-118) TFA is a peptide inhibitor operating noncompetitively against protein kinase C (PKC), exhibiting inhibitory concentrations (IC50) in the range of 28-62 μM [1].
价 格：￥电议型 号：T75887产 地：中国大陆
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T75886[Ala107]MBP(104-118) TFA；化合物 [Ala107]MBP(104-118) TFA[Ala107]MBP(104-118) TFA
[Ala107]MBP(104-118) TFA is a noncompetitive peptide inhibitor of protein kinase C (PKC), exhibiting IC50 values between 46-145 μM.
价 格：￥电议型 号：T75886产 地：中国大陆
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T75845[Ala17]-MCH TFA；化合物 [Ala17]-MCH TFA[Ala17]-MCH TFA
[Ala17]-MCH TFA, a selective ligand for MCHR 1 (K i =0.16 nM) over MCHR 2 (K i =34 nM), is an analogue of MCH. When labeled with a [Eu 3+ chelate], [Ala17]-MCH exhibits high affinity for MCHR 1 (K d =0.37 nM) and negligible binding affinity for MCHR 2.
价 格：￥电议型 号：T75845产 地：中国大陆
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T75777187-1, N-WASP inhibitor TFA；化合物 187-1, N-WASP inhibitor TFA187-1, N-WASP inhibitor TFA
187-1, N-WASP Inhibitor TFA, a 14-amino acid cyclic peptide, serves as an allosteric inhibitor of the neural Wiskott-Aldrich syndrome protein (N-WASP). This compound effectively suppresses actin assembly triggered by phosphatidylinositol 4,5-bisphosphate (PIP2), exhibiting a potent inhibitory concentration (IC 50) of 2 μM. Furthermore, 187-1, N-WASP Inhibitor TFA inhibits the activation of the Arp2/3 complex by N-WASP, maintaining the protein in its autoinhibited state, ensuring the prevention o
价 格：￥电议型 号：T75777产 地：中国大陆
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T75772[Ala1,?3,?11,?15]?-?Endothelin (53-63) (TFA)；化合物 [Ala1,?3,?11,?15]?-?Endothelin (53-63) (TFA)[Ala1,?
[Ala1,3,11,15]-Endothelin (53-63) (TFA) is a selective ET B agonist with IC50 values ranging from 0.33 nM to 0.61 nM, demonstrating its preference for ET B receptors. It is utilized in the study of vasoconstriction.
价 格：￥电议型 号：T75772产 地：中国大陆
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T7556611-Oxomogroside II A1；化合物 11-Oxomogroside II A111-Oxomogroside II A1
11-Oxomogroside II A1 (compound 7), an oxidized cucurbitin derived from the ethanol extract of Rohanberry fruit, serves as an inhibitor for the activation of Epstein-Barr virus (EBV) early antigen (EBV-EA) triggered by 12-O-tetradecanoylphorbol-13-acetate (TPA). Additionally, it has a modest ability to inhibit the activation of (±)-(E)-methyl-2-[(E)-hydroxyimino]-5-nitro-6-methoxy-3-hexemide (NOR 1), a nitric oxide (NO) donor [1].
价 格：￥电议型 号：T75566产 地：中国大陆
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T75417alpha-1,3-Galactosyltransferase (a1,3GalT)；化合物 alpha-1,3-Galactosyltransferase (a1,3GalT)alpha-1,3-G
Alpha-1,3-Galactosyltransferase (a1,3GalT) (GGTA1) catalyzes the synthesis of the α-gal epitope by transferring a galactose (Gal) molecule in an α1-3 linkage from a uridyl-diphosphate (UDP) donor to the N-acetyllactosamine (Galβ1,4GlcNAc-R) on glycoproteins. This enzyme is essential for the production of the α-galactose (α-Gal) epitope, a biomolecule prevalent in most mammalian species [1].
价 格：￥电议型 号：T75417产 地：中国大陆
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T74859SLC7A11-IN-1；化合物 SLC7A11-IN-1SLC7A11-IN-1
SLC7A11-IN-1 is a potent inhibitor of the solute carrier family 7 member 11 (SLC7A11, xCT), exhibiting antiproliferative, anti-tumor activities, and the ability to inhibit cell invasion and metastasis. It induces apoptosis and arrests cell cycle progression in the S-phase [1].
价 格：￥电议型 号：T74859产 地：中国大陆
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T74701A18-Iso5-2DC18；化合物 A18-Iso5-2DC18A18-Iso5-2DC18
A18-Iso5-2DC18 (compound A18), a lipidoid, enhances mRNA protein expression and induces a robust immune response [1].
价 格：￥电议型 号：T74701产 地：中国大陆
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T73531SABA1；化合物 SABA1SABA1
SABA1 demonstrates antibacterial efficacy against Pseudomonas aeruginosa and Escherichia coli, achieving an IC50 value of 4.0 ?M against E. coli ACC.
价 格：￥电议型 号：T73531产 地：中国大陆
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T72661A1AT modulator 2；化合物 A1AT modulator 2A1AT modulator 2
A1AT Modulator 2, an α-1 antitrypsin (A1AT) modulator, exhibits an IC50 value greater than 1.0 μM and an EC50 value less than 0.4 μM. It is utilized in the study of infection and inflammation.
价 格：￥电议型 号：T72661产 地：中国大陆
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T72501CYP4A11/CYP4F2-IN-1；CYP4A11/CYP4F2 抑制剂 1CYP4A11/CYP4F2-IN-1
CYP4A11/CYP4F2-IN-1 is a cytochrome P450 (CYP) 4A11 and CYP4F2 inhibitor. CYP4A11/CYP4F2-IN-1 can be used to study kidney diseases and cardiovascular and cerebrovascular diseases.
价 格：￥电议型 号：T72501产 地：中国大陆
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T72195KCa1.1 channel activator-2；化合物 KCa1.1 channel activator-2KCa1.1 channel activator-2
KCa1.1 channel activator-2, a hybrid derivative of Quercetin, selectively stimulates the vascular KCa1.1 channels. This compound demonstrates significant myorelaxant activity.
价 格：￥电议型 号：T72195产 地：中国大陆
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T72194KCa1.1 channel activator-1；化合物 KCa1.1 channel activator-1KCa1.1 channel activator-1
KCa1.1 Channel Activator-1, a hybrid derivative of Quercetin, selectively stimulates the vascular KCa1.1 channels while also blocking CaV1.2 channels. Additionally, it demonstrates weak myorelaxant activity.
价 格：￥电议型 号：T72194产 地：中国大陆
