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T75900CART(55-102)(rat) TFA；化合物 CART(55-102)(rat) TFACART(55-102)(rat) TFA
CART(55-102)(rat) TFA, a rat-derived satiety factor, exhibits potent appetite-suppressing properties. This compound is intricately linked to both leptin and neuropeptide Y, playing a crucial role in the regulation of hunger. Moreover, CART(55-102)(rat) TFA has been identified to induce anxiety and stress-related behavior, as documented in studies [1] [2].
价 格：￥电议型 号：T75900产 地：中国大陆
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T73900(±)-Alliin；化合物 (±)-Alliin(±)-Alliin
(±)-Alliin, the principal active component in garlic, functions as a potential inhibitor of SARS-CoV-2´s main protease (Mpro) [1].
价 格：￥电议型 号：T73900产 地：中国大陆
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T7365Inarigivir；化合物InarigivirORI-9020|||SB-9000；ORI-9020|||SB-9000
Inarigivir (ORI-9020) is a dinucleotide that can significantly reduce liver HBV DNA.
价 格：￥电议型 号：T7365产 地：中国大陆
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T72900Indolokine A4；化合物 Indolokine A4Indolokine A4
Indolokine A4, a catabolite of indole-3-pyruvate (I3P), is a potent AhR agonist [1] .
价 格：￥电议型 号：T72900产 地：中国大陆
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T71614FR 900452；化合物 FR 900452FR 900452
FR 900452 is a platelet activating factor antagonist from fermentatiion products of Streptomyces phaeofaciens.
价 格：￥电议型 号：T71614产 地：中国大陆
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T71259GNE-900；化合物GNE-900GNE900|||GNE 900；GNE900|||GNE 900
GNE-900 is an ATP-competitive ChK1 inhibitor with selective and oral activity.GNE-900 inhibits ChKl and ChK2 with IC50 values of 0.0011 and 1.5 ?M, respectively.GNE-900 enhances DNA damage and induces apoptosis. GNE-900 has antitumor activity.
价 格：￥电议型 号：T71259产 地：中国大陆
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T71201SCH-900822；化合物 SCH-900822SCH-900822
SCH-900822 is a potent and selective glucagon receptor antagonist.
价 格：￥电议型 号：T71201产 地：中国大陆
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T70900VT-ME6；化合物 VT-ME6VT-ME6
VT-ME6 is a potent and selective sphingosine kinase 2 inhibitor. VT-ME6, contained a quaternary ammonium group as a warhead and established that a positively charged moiety is necessary for engaging key amino acid residues in the enzyme binding pocket.13,14 This compound is moderately potent (Ki = 8 lM) and displays three-fold selectivity for SphK2 over SphK1. Sphingosine-1-phosphate (S1P) is a ubiquitous, endogenous small molecule that is synthesized by two isoforms of sphingosine kinase (SphK
价 格：￥电议型 号：T70900产 地：中国大陆
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T70678Rwj 29009；化合物 Rwj 29009Rwj 29009
Rwj 29009 is a potassium channel activator with prominent coronary and peripheral vasodilating actions.
价 格：￥电议型 号：T70678产 地：中国大陆
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T70363PF-06371900；化合物 PF-06371900PF-06371900
PF-06371900 is a potent and highly selective inhibitor of leucine-rich repeat kinase 2 (LRRK2).
价 格：￥电议型 号：T70363产 地：中国大陆
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T69900GUN 00775；化合物 GUN 00775GUN 00775
GUN 00775, also known as N-(m-PEG4)-3,3-Dimethyl-3H-indole-N´-(acid-PEG3)-Benzothiazole Cy5, is a PEG derivative containing a cyanine dye with excitation/emission maximum 649/667 nm and a free terminal carboxyl acid. Terminal carboxylic acid can react with primary amine groups in the presence of of activators (e.g. EDC, or DCC) to form a stable amide bond. The hydophilic PEG spacer increases solubility in aqueous media. This product has no formal name at the moment. For the convenience of
价 格：￥电议型 号：T69900产 地：中国大陆
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T69769BDP8900；化合物 BDP8900BDP8900
BDP8900 is a potent and selective MRCK inhibitor, reducing substrate phosphorylation. BDP8900 leads to morphological changes in cancer cells along with inhibition of their motility and invasive character.
价 格：￥电议型 号：T69769产 地：中国大陆
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T69009Gnidimacrin；化合物 GnidimacrinGnidimacrin
Gnidimacrin activated HIV-1 replication and killed persistently-infected cells at picomolar concentrations. In addition to its potential to purge HIV-1 from latently infected cells, gnidimacrin potently inhibited a panel of HIV-1 R5 virus infection of peripheral blood mononuclear cells (PBMCs) at an average concentration lower than 10 pM. These results suggest that gnidimacrin could activate latent HIV-1, specifically kill HIV-1 persistently infected cells, and inhibit R5 viruses at picomolar c
价 格：￥电议型 号：T69009产 地：中国大陆
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T69008Paroxol methanesulfonate；化合物 Paroxol methanesulfonateParoxol methanesulfonate
Paroxol methanesulfonate is an intermediate in the synthesis of Paroxetine, a selective serotonin reuptake inhibitor.
价 格：￥电议型 号：T69008产 地：中国大陆
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T69007Indeloxazine；化合物 IndeloxazineIndeloxazine
Indeloxazine is a cerebral activator and anticonvulsant.
价 格：￥电议型 号：T69007产 地：中国大陆
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T69006Atorvastatin lysine；化合物 Atorvastatin lysineAtorvastatin lysine
Atorvastatin lysine is a selective and competitive HMGCR (HMG-CoA reductase) inhibitor.
价 格：￥电议型 号：T69006产 地：中国大陆
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T69005CEP-6800；化合物 CEP-6800CEP-6800
CEP-6800 is a potent PARP inhibitor with potential anticancer activity. CEP-6800 could be used as a chemopotentiating agent with a variety of clinically effective chemotherapeutic agents.
价 格：￥电议型 号：T69005产 地：中国大陆
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T69004Falipamil hydrochloride；化合物 Falipamil hydrochlorideFalipamil hydrochloride
Falipamil hydrochloride is a calcium channel antagonist potentially for the treatment of ischaemic heart disorder and sinus.
价 格：￥电议型 号：T69004产 地：中国大陆
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T69003E7974；化合物 E7974E7974
E7974 is an analog of the sponge-derived anti-microtubule tripeptide hemiasterlin with antimitotic and potential antineoplastic activities. Hemiasterlin analog E7974 binds to the Vinca domain on tubulin, resulting in inhibition of tubulin polymerization and microtubule assembly; depolymerization of exsiting microtubules; inhibition of mitosis; and inhibition of cellular proliferation. This agent may have more affinity for the beta-3 tubulin isotype. Check for active clinical trials or closed cli
价 格：￥电议型 号：T69003产 地：中国大陆
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T69002Zimeldine hydrochloride hydrate；化合物 Zimeldine hydrochloride hydrateZimeldine hydrochloride hydrate
Zimeldine hydrochloride hydrate is a serotonin uptake inhibitor that was formerly used for depression but was withdrawn worldwide in September 1983 because of the risk of Guillain-Barre Syndrome associated with its use.
价 格：￥电议型 号：T69002产 地：中国大陆
