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T16528PI-828；化合物PI-828LY 294002, 4gamma-NH2；LY 294002, 4gamma-NH2
PI-828 is a phosphatidylinositol 3-kinase (PI3K) inhibitor, which is widely used to study the physiological function of PI3K and also promotes stem cell differentiation into mesoderm.
价 格：￥电议型 号：T16528产 地：中国大陆
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T16125MMV390048；化合物MMV390048MMV390048
MMV390048 is an antimalarial agent and is a representative of a new chemical class of Plasmodium PI4K inhibitor (Kdapp=0.3 μM). MMV390048 binds to the ATP binding site of Plasmodium PI4K and does not bind to other P. falciparum and human kinases apart from human PIP4K2C, thus alleviating potential kinase-mediated safety concerns.
价 格：￥电议型 号：T16125产 地：中国大陆
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T16124MMP13-IN-3；化合物MMP13-IN-3MMP13-IN-3
MMP13-IN-3 is >1000 selective over other MMPs. MMP13-IN-3 is an effective, selective, and orally active MMP-13 inhibitor (IC50=1 nM) for the potential treatment of osteoarthritis.
价 格：￥电议型 号：T16124产 地：中国大陆
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T16123MMG-11；化合物 T16123MMG-11
MMG-11 inhibits both TLR2/1 and TLR2/6 signaling (IC50s: 1.7 μM for Pam3CSK4-induced hTLR2/1 and 5.7 μM for Pam2CSK4-induced hTLR2/6 responses). MMG-11 is an effective and selective human TLR2 antagonist with low cytotoxicity.
价 格：￥电议型 号：T16123产 地：中国大陆
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T16122MMAF sodium；化合物 T16122Monomethylauristatin F sodium；Monomethylauristatin F sodium
MMAF sodium is widely used as a cytotoxic component of antibody-drug conjugates (ADCs) such as Vorsetuzumab mafodotin and SGN-CD19A. MMAF sodium is an effective tubulin polymerization inhibitor and is used as an antitumor agent.
价 格：￥电议型 号：T16122产 地：中国大陆
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T16121MMAF Hydrochloride；化合物 T16121Monomethylauristatin F Hydrochloride；Monomethylauristatin F Hydrochlori
MMAF Hydrochloride is widely used as a cytotoxic component of antibody-drug conjugates (ADCs) such as Vorsetuzumab mafodotin and SGN-CD19A. MMAF Hydrochloride is an effective tubulin polymerization inhibitor and is used as an antitumor compound.
价 格：￥电议型 号：T16121产 地：中国大陆
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T16031McMMAF；化合物McMMAFMaleimidocaproyl monomethylauristatin F；Maleimidocaproyl monomethylauristatin F
McMMAF is a protective group-conjugated MMAF. MMAF is a potent tubulin polymerization inhibitor.It is a MMAF derivative having a Maleimidocaproyl linker (MC linker), which is ready to conjugate to antibody or other proteins or biopolymers. Mafodotin is a useful agent for make antibody drug conjugate (ADC) for targeted drug delivery.
价 格：￥电议型 号：T16031产 地：中国大陆
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T15697L-NMMA acetate；化合物L-NMMA acetateTilarginine acetate|||Methylarginine acetate；Tilarginine acetate|||M
L-NMMA acetate (Tilarginine acetate) is an inhibitor of nitric oxide synthase of all NOS isoforms (i.e. NOS1, NOS2, and NOS3). The Ki values are 0.18, 0.4, and 6 ?M for nNOS, eNOS, and iNOS, respectively.
价 格：￥电议型 号：T15697产 地：中国大陆
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T15541Hyperforin dicyclohexylammonium salt；化合物 T15541Hyperforin DCHA；Hyperforin DCHA
Hyperforin dicyclohexylammonium salt is a transient receptor canonical 6 channel activator with antidepressant effect. It modulates Ca2+ levels by activating Ca2+-conducting non-selective canonical TRPC6 channels.
价 格：￥电议型 号：T15541产 地：中国大陆
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T15391Glufosinate ammonium；草铵膦Glufosinate ammonium
Glufosinate ammonium is a phosphinic acid analogue of glutamic acid and is an herbicide. Glufosinate ammonium is converted by plant cells into PT (L-phosphinothricin). Glufosinate ammonium has neurotoxic activity.
价 格：￥电议型 号：T15391产 地：中国大陆
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T15369Lgamma-DGG acetate(6729-55-1 free base)；化合物gamma-DGG acetateγDGG|||γ-D-Glutamylglycine；γDGG|||γ-D-Glu
gamma-DGG acetate(6729-55-1 free base) (γ-D-Glutamylglycine) is a competitive blocker of AMPA receptor.
价 格：￥电议型 号：T15369L产 地：中国大陆
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T15369gamma-DGG化合物 T15369γDGG|||γ-D-Glutamylglycine
gamma-DGG is a competitive blocker of AMPA receptor.
价 格：￥电议型 号：T15369产 地：中国大陆
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T15337Forodesine呋咯地辛Immucillin-H|||BCX-1777
Forodesine (BCX-1777) is an orally active and potent purine nucleoside phosphorylase (PNP) inhibitor, a new purine nucleoside analog, inhibitor of human lymphocyte proliferation, induces apoptosis in leukemic cells by increasing dGTP levels, and may be useful in the study of cutaneous T-cell lymphomas.
价 格：￥电议型 号：T15337产 地：中国大陆
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T15055DB04760；化合物 DB04760MMP-13 Inhibitor；MMP-13 Inhibitor
DB04760 is a highly selective, non-zinc-chelating inhibitor of MMP-13 (IC50: 8 nM). DB04760 obviously decreases paclitaxel neurotoxicity and has anticancer activity.
价 格：￥电议型 号：T15055产 地：中国大陆
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T14932L1Ceruletide Ammonium Salt；化合物Ceruletide Ammonium SaltCaerulein Ammonium Salt|||Ceruletide Ammonium Sa
Ceruletide Ammonium Salt is a decapeptide, originating from the skin of tropical frogs, which is a potent cholecystokinin receptor agonist and a safe and effective cholecystokinin receptor agonist with direct spasmodic effects on the gallbladder muscle and bile ducts. Ceruletide Ammonium Salt has sedative activity and has been used in the study of chronic schizophrenia.Ceruletide Ammonium Salt is a decapeptide, originating from the skin of tropical frogs.
价 格：￥电议型 号：T14932L1产 地：中国大陆
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T14932LCeruletide Ammonium acetate；化合物Ceruletide Ammonium acetateFI-6934 Ammonium acetate|||Caerulein Ammon
Ceruletide Ammonium acetate (FI-6934 Ammonium acetate) is a cholecystokinin (CCK) receptor agonist. Ceruletide Ammonium acetate is a safe and effective cholecystokinetic agent and small bowel and exocrine pancreatic stimulant.
价 格：￥电议型 号：T14932L产 地：中国大陆
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T14322ARP-100；化合物ARP-100MMP-2 Inhibitor III；MMP-2 Inhibitor III
ARP-100 (MMP-2 Inhibitor III) is a potent and selective matrix metalloproteinase MMP-2 inhibitor (IC50=12 nM). ARP-100 interacts with the S1´ pocket of MMP-2 and exhibits anti-invasive properties in an in vitro invasion Matrigel model. ARP-100 has low inhibitory activity against MMP-1 (>50 μM), MMP-3 (4.5 μM), MMP-7 (>50 μM) and MMP-9 (0.2 μM)[1][2].
价 格：￥电议型 号：T14322产 地：中国大陆
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T1431Khellin；呋喃并色酮Amicardine|||Methafrone|||Visammin；凯林|||Amicardine|||Methafrone|||Visammin
Khellin (Methafrone) is a vasodilator that also has bronchodilatory action.
价 格：￥电议型 号：T1431产 地：中国大陆
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T1406Amantadine hydrochloride；盐酸金刚烷胺1-adamantanamine HCl|||1-Adamantanamine hydrochloride|||Symmetrel|||C
Amantadine hydrochloride (CI-719) is an antiviral that is used in the prophylactic or symptomatic treatment of influenza A and Parkinson disease.
价 格：￥电议型 号：T1406产 地：中国大陆
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T13951UCB-9260；化合物UCB-9260cytotoxicity|||asymmetric|||trimer|||Inhibitor|||neutrophil|||autoimmune|||UCB92
UCB-9260 inhibits TNF signaling by stabilizing an asymmetric form of the trimer.
价 格：￥电议型 号：T13951产 地：中国大陆
