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T6374Alfacalcidol；阿法骨化醇Bondiol|||Etalpha|||1-hydroxy Vitamin D3|||1.alpha.-Hydroxyvitamin D3|||1-hydroxyc
Alfacalcidol (Etalpha) (1-hydroxycholecalciferol; Alpha D3; 1.alpha.-Hydroxyvitamin D3) is a non-selective VDR activator medication.
价 格：￥电议型 号：T6374产 地：中国大陆
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T63606Cav 3.2 inhibitor 2；化合物 Cav 3.2 inhibitor 2Cav 3.2 inhibitor 2
Cav 3.2 inhibitor 2 is an inhibitor of Cav3.2 T-type Ca2+channels with an IC50=0.09339 μM at a constant potential of -80 mV. Cav 3.2 inhibitor 2 exhibits potent inhibition of T-channel-dependent somatic and visceral pain in mice. inhibitor 2 can be used to study intractable pain.
价 格：￥电议型 号：T63606产 地：中国大陆
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T63350Cav 3.2 inhibitor 3；化合物 Cav 3.2 inhibitor 3Cav 3.2 inhibitor 3
Cav 3.2 inhibitor 3 is a potent inhibitor of the Cav3.2 T-type Ca2+channel (IC50: 0.1534 μM) and has a low binding affinity for D2 receptors.
价 格：￥电议型 号：T63350产 地：中国大陆
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T63186Cav 3.2 inhibitor 1；化合物 Cav 3.2 inhibitor 1Cav 3.2 inhibitor 1
Cav 3.2 inhibitor 1 is a T-type calcium channel inhibitor with low binding affinity for the dopamine receptor (D2 receptor.) Cav 3.2 inhibitor 1 can be used in studies of physical and visceral pain.
价 格：￥电议型 号：T63186产 地：中国大陆
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T63049CHD1Li 6.11；化合物CHD1Li 6.11CHD1Li 6.11
CHD1Li 6.11 is a potent inhibitor of oncogenic CHD1L, acting on the cat-CHD1L recombinant protein (IC50: 3.3 μM). CHD1Li 6.11 is an orally active antitumour agent that significantly reduces the tumour volume of CRC xenografts generated from isolated quasi-mesenchymal cells (M phenotype) with enhanced tumourigenic properties. These cells have enhanced tumourigenic properties.
价 格：￥电议型 号：T63049产 地：中国大陆
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T62827BCP-T.A；化合物 BCP-T.ABCP-T.A
BCP-T.A is a heterocyclic electrophile that binds GPX4 and thus effectively induces iron death (ferroptosis).
价 格：￥电议型 号：T62827产 地：中国大陆
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T62586Cav 2.2/3.2 blocker 1；化合物 Cav 2.2/3.2 blocker 1Cav 2.2/3.2 blocker 1
Cav 2.2/3.2 blocker 1 (Compound 9e) is a neuronal calcium channel blocker that acts on Cav2.2 (IC50: 1.22 μM) and Cav3.2 (IC50: 80 μM). Can penetrate the central nervous system.
价 格：￥电议型 号：T62586产 地：中国大陆
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T62422Nav1.8-IN-2；化合物 Nav1.8-IN-2Nav1.8-IN-2
Nav1.8-IN-2 (compound 35A) is a potent inhibitor of Nav1.8 (IC50: 0.4 nM). Nav1.8-IN-2 can be used in studies of pain disorders, cough, acute and chronic pruritus.
价 格：￥电议型 号：T62422产 地：中国大陆
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T6112Doxercalciferol；度骨化醇TSA 840|||Hectorol|||1.alpha.-Hydroxyvitamin D2|||1α-hydroxyvitamin D2；TSA 840||
Doxercalciferol (TSA 840) is a synthetic vitamin D2 analog, suppressing parathyroid synthesis and secretion, used to treat secondary hyperparathyroidism and metabolic bone disease.
价 格：￥电议型 号：T6112产 地：中国大陆
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T61026CaV1.3 antagonist-1；化合物 CaV1.3 antagonist-1CaV1.3 antagonist-1
CaV1.3 antagonist-1 is a cyclopentyl derivative with the potential for the research of Parkinson´s disease. CaV1.3 antagonist-1 inhibits Ca V 1.3 LTCC over 600-fold more effectively than Ca V 1.2 LTCC. CaV1.3 antagonist-1 is a potent and highly selective antagonist of Ca V 1.3 L-type calcium channel (LTCC) with an IC50 value of 1.7 μM [1].
价 格：￥电议型 号：T61026产 地：中国大陆
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T60636Pitolisant；替洛利生Tiprolisant|||BF-2.649|||BF-2649；Tiprolisant|||BF-2.649|||BF-2649
Pitolisant (Tiprolisant) is a selective and potent non-imidazole recombinant human histamine H3 receptor antagonist for the study of excessive daytime sleepiness and sudden collapse in patients with episodic narcolepsy.
价 格：￥电议型 号：T60636产 地：中国大陆
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T60112H-Glu(OEt)-OEt.HClL-谷氨酸二乙酯盐酸盐Diethyl L-glutamate hydrochloride|||(S)-Diethyl 2-aminopentanedioate hy
H-Glu(OEt)-OEt.HCl (Diethyl L-glutamate hydrochloride) is a glutamic acid derivative.
价 格：￥电议型 号：T60112产 地：中国大陆
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T5956VP3.15 dihydrobromide；化合物VP3.15 dihydrobromideVP3.15 dihydrobromide
VP3.15 dihydrobromide is a potent, orally bioavailable and CNS-penetrant dual phosphodiesterase (PDE7- glycogen synthase kinase (GSK)3 inhibitor(with IC50s of 1.59 μM , 0.88 μM,respectively.)
价 格：￥电议型 号：T5956产 地：中国大陆
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T5512JNJ16259685；化合物JNJ16259685.TN.T 16259685；.TN.T 16259685
JNJ16259685 (TN.T 16259685) is a selective mGluR1 antagonist, and inhibits the synaptic activation of mGluR1 in a concentration-dependent manner with IC50 of 19 nM.
价 格：￥电议型 号：T5512产 地：中国大陆
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T5486RU.521；化合物RU320521RU320521；RU320521
RU.521 (RU3205217) is a potent dsDNA inhibitor (IC50 : 700 nM), inhibition of the dsDNA pathway by RU.521 requires the presence of cGAS.
价 格：￥电议型 号：T5486产 地：中国大陆
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T501153-phenoxy-8-azabicyclo[3.2.1]octane HCl；3-phenoxy-8-azabicyclo[3.2.1]octane 盐酸盐3-phenoxy-8-azabicycl
3-phenoxy-8-azabicyclo[3.2.1]octane hydrochloride is a synthetic compound belonging to the class of azabicyclooctanes. It is a potent and selective agonist of the dopamine D2 receptor and is widely used to study the mechanisms of dopamine signaling and its role in various physiological and pathological processes.
价 格：￥电议型 号：T50115产 地：中国大陆
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T4866H-Trp-NH2.HCl；L-色氨酰胺盐酸盐L-Tryptophanamide hydrochloride|||(2S)-2-amino-3-(1H-indol-3-yl)propanamide h
H-Trp-NH2.HCl ((2S)-2-amino-3-(1H-indol-3-yl)propanamide hydrochloride) is an endogenous metabolite that has been detected in various biological fluids, e.g. Urine and blood.
价 格：￥电议型 号：T4866产 地：中国大陆
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T4248T.cruzi Inhibitor (1350920-22-7(free base))；T.cruzi InhibitorT.cruzi Inhibitor (1350920-22-7(free ba
T.cruzi Inhibitor is a Trypanosoma cruzi inhibitor.
价 格：￥电议型 号：T4248产 地：中国大陆
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T4198T.cruzi-IN-1；T.cruzi InhibitorMDK1088|||T.cruzi Inhibitor；MDK1088|||T.cruzi Inhibitor
T.cruzi-IN-1 (MDK1088) is a Trypanosoma cruzi inhibitor.
价 格：￥电议型 号：T4198产 地：中国大陆
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T41078Lipopolysaccharides, Escherichiacoli；脂多糖 来源于大肠杆菌Lipopolysaccharide, E. coli O111:B4；Lipopolysacchari
Lipopolysaccharides, Escherichiacoli (E. coli O111:B4) is a unique component of the cell wall of Gram-negative bacteria, consisting of three regions: lipid A, oligosaccharide core and O-specific polysaccharide (O-antigen). Lipopolysaccharides, Escherichiacoli helps maintain the integrity of the outer cell membrane and protects bacteria from damage by bile salts and lipid antibiotics. Lipopolysaccharides, Escherichiacoli is a highly immunogenic antigen that can enhance immune responses and can be
价 格：￥电议型 号：T41078产 地：中国大陆
