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T40111LBMS-1166-N-piperidine-CO-N-piperazine dihydrochloride；化合物T40111LBMS-1166-N-piperidine-CO-N-piperazin
BMS-1166-N-piperidine-CO-N-piperazine dihydrochloride is a resorcinol di-Ph ether scaffold-based programmed cell death-1 (PD-1)/programmed cell death ligand 1 (PD-L1) inhibitor that inhibits the PD-1/PD-L1 interaction with an IC50 of 39.2 nM.BMS-1166-N-piperidine-CO-N-piperazine dihydrochloride contains the target protein PD-1/PD-L1 ligand and PROTAC linker.BMS-1166-N-piperidine-CO-N-piperazine dihydrochloride can be used to synthesize PROTAC linker. BMS-1166-N-piperidine-CO-N-piperazine dihydro
价 格：￥电议型 号：T40111L产 地：中国大陆
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T40111BMS-1166-N-piperidine-CO-N-piperazine；BMS-1166-N-piperidine-CO-N-piperazineBMS-1166-N-piperidine-CO-
BMS-1166-N-piperidine-CO-N-piperazine is a chemical compound that contains a PD-1/PD-L1 immune checkpoint ligand and a PROTAC linker. It can be utilized in the synthesis of PROTAC PD-1/PD-L1 degrader-1, which effectively inhibits the PD-1/PD-L1 interaction, demonstrating an IC50 value of 39.2 nM.
价 格：￥电议型 号：T40111产 地：中国大陆
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T3S1117Pseudoaspidin；伪绵马素Pseudoaspidin
Pseudoaspidin is isolated from fern plants.
价 格：￥电议型 号：T3S1117产 地：中国大陆
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T3977LLifitegrast sodium化合物 T3977LSAR-1118-023|||SAR1118-023|||SAR 1118-023|||Xiidra
Lifitegrast sodium (SAR-1118) is an LFA-1 antagonist for the therapy of vascular complications of the eye. It inhibits T cell-mediated inflammation by blocking the binding of two cell surface proteins (lymphocyte function-associated antigen 1 and intercellular adhesion molecule 1), thus reducing overall inflammatory responses.
价 格：￥电议型 号：T3977L产 地：中国大陆
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T3977Lifitegrast；立他司特SHP-606|||SAR 1118；SHP-606|||SAR 1118|||立他司特|||利非司特
Lifitegrast (SAR 1118) is a lymphocyte, function-associated antigen-1 antagonist.
价 格：￥电议型 号：T3977产 地：中国大陆
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T39111Fmoc-D-Trp(Boc)-OH；Fmoc-D-Trp(Boc)-OHFmoc-D-Trp(Boc)-OH
Fmoc-D-Trp(Boc)-OH is a labile ADC linker employed for synthesizing antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T39111产 地：中国大陆
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T38111Dimethyl-W84 (dibromide)；Dimethyl-W84 (dibromide)Dimethyl-W84 (dibromide)；Dimethyl-W84 (dibromide)
Dimethyl-W84 is a selective allosteric modulator of the M2 muscarinic acetylcholine receptor. It hinders the dissociation of the orthosteric antagonist N-methylscopolamine from the M2 receptor with an EC50 value of 3 nM.
价 格：￥电议型 号：T38111产 地：中国大陆
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T38005P11149；P11149P11149
P11149, a derivative of Galanthamine, acts as a competitive, orally active, and selective AChE inhibitor with the ability to weakly penetrate the blood-brain barrier (BBB). It demonstrates selective inhibition, exhibiting an IC50 of 1.3 μM for rat BChE/AChE, and shows central cholinergic activity, behavioral efficacy, and safety. P11149 is utilized in Alzheimer’s disease research[1].
价 格：￥电议型 号：T38005产 地：中国大陆
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T37819Brain-Derived Acidic Fibroblast Growth Factor (102-111) (bovine) (trifluoroacetate salt)；Brain-Deriv
Brain-derived acidic fibroblast growth factor (102-111) is a peptide fragment of brain-derived acidic fibroblast growth factor (aFGF). aFGF is an angiogenic vascular endothelial cell mitogen produced in bovine brain that has sequence homology to interleukin-1. It also shares sequence homology with the known neuropeptides neuromedin C , bombesin , neuromedin K , substance K , substance P , physalaemin, and eledoisin. aFGF (102-111) corresponds to amino acid residues 102-111 of the fulllength pept
价 格：￥电议型 号：T37819产 地：中国大陆
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T37111Corticotropin-releasing factor (human) (acetate)；Corticotropin-releasing factor (human) (acetate)Cor
Human CRF acetate is a chemical compound that effectively stimulates the synthesis and secretion of adrenocorticotropin in the anterior pituitary.
价 格：￥电议型 号：T37111产 地：中国大陆
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T3677011-deoxy Prostaglandin E1；11-deoxy Prostaglandin E111-deoxy Prostaglandin E1；11-deoxy Prostaglandin
11-deoxy Prostaglandin E1 is a prostaglandin E1 analogue that has bronchodilator activity and can inhibit histamine-induced bronchoconstriction and cause relaxation of tracheal strips in isolated guinea pigs.
价 格：￥电议型 号：T36770产 地：中国大陆
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T36376SB-612111；SB-612111SB-612111
SB-612111 is a novel and potent human opiate receptor-like orphan receptor (ORL-1) antagonist with a high affinity for hORL-1 (Ki=0.33 nM). SB-612111 exhibits selectivity for μ-, κ- and δ-receptors with Ki values of 57.6 nM, 160.5 nM and 2109 nM, respecticely. SB-612111 effectively antagonizes the pronociceptive action of Nociceptin in an acute pain model[1].
价 格：￥电议型 号：T36376产 地：中国大陆
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T36111L-Iduronic acid sodium salt；L-艾杜糖醛酸钠L-Iduronic acid sodium salt
L-Iduronic acid sodium salt is a monosaccharide that is an important component of glycosaminoglycans (GAGs) such as heparin, heparan sulfate, and dermatan sulfate.
价 格：￥电议型 号：T36111产 地：中国大陆
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T35254YM 11133；化合物 T35254YM-11133|||YM11133；YM-11133|||YM11133
YM 11133 is a biochemical.
价 格：￥电议型 号：T35254产 地：中国大陆
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T35253YM 11124；化合物 T35253YM-11124|||YM11124；YM-11124|||YM11124
YM 11124 is a biochemical.
价 格：￥电议型 号：T35253产 地：中国大陆
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T35111Way 125971；化合物 T35111Way-125971|||Way125971；Way-125971|||Way125971
Way 125971 is a bioactive chemcial.
价 格：￥电议型 号：T35111产 地：中国大陆
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T34710STA 2；化合物 T34710ONO 11113|||STA-2|||STA2；ONO 11113|||STA-2|||STA2
STA 2 is an analogue of TXA2, a thromboxane receptor in the colonic epithelium.
价 格：￥电议型 号：T34710产 地：中国大陆
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T34658SLP7111228；化合物 T34658SLP-7111228|||SLP 7111228；SLP-7111228|||SLP 7111228
SLP7111228 is an effective and selective SphK1 inhibitor (Ki = 48 nM).
价 格：￥电议型 号：T34658产 地：中国大陆
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T34592Sdz 215-811；化合物 T34592Sdz-215-811|||Pentatreotide|||Sdz215-811|||Octreoscan 111；Sdz-215-811|||Pentat
Sdz 215-811 is a potential radiopharmaceutical used in somatostatin receptor-positive tumors imaging.
价 格：￥电议型 号：T34592产 地：中国大陆
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T34111Ponfibrate；化合物 T34111Ponfibrate
Ponfibrate is a hypobetalipoproteinemic and Lipid decreasing agent.
价 格：￥电议型 号：T34111产 地：中国大陆
