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T28077MMPP；化合物 MMPPMMPP
MMPP is a novel VEGFR2 inhibitor with anti-inflammatory and potential anticancer activity, inhibits STAT3, inhibits angiogenesis via VEGFR2/AKT/ERK/NF-kappaB pathway, and can be used to alleviate myocardial injury.
价 格：￥电议型 号：T28077产 地：中国大陆
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T28075MM-206化合物 T28075MM206|||MM 206
MM-206, a cell-permeable, non-cytotoxic naphthalene sulfonamide compound, it effectively inhibits STAT3 DNA-binding activity.
价 格：￥电议型 号：T28075产 地：中国大陆
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T27975MAL-PEG4-MMAF；化合物 T27975MAL-PEG4-MMAF
MAL-PEG4-MMAF is a maleimido functionalized derivative of MMAF (Monomethyl auristatin F) with PEG4 linker. The maleimido functional group can be easily conjugated to protein carriers (such as antibody or enzyme). MAL-PEG4-MMAF is a useful precursor for making antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T27975产 地：中国大陆
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T27177Dimethyl ceanothate；化合物 T27177dimethyl emmolate；dimethyl emmolate
Dimethyl ceanothate shows moderate to low leishmanicidal and trypanocidal activities.
价 格：￥电议型 号：T27177产 地：中国大陆
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T26977CeMMEC2；化合物 T26977CeMMEC-2|||CeMMEC 2；CeMMEC-2|||CeMMEC 2
CeMMEC2, a novel inhibitor of BRD4, binds both the first and the second bromodomain of BRD4.
价 格：￥电议型 号：T26977产 地：中国大陆
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T26772Tacitin；化合物TacitinTacitin|||Benzoctamine HCl|||Methyl(methyl-9,10-ethano-9(10H)-anthryl)ammonium chl
Tacitin (Benzoctamine Hydrochloride) shows sedative and anti-anxiety properties. Tacitin blocks the central postsynaptic serotonin receptors.
价 格：￥电议型 号：T26772产 地：中国大陆
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T26521ABP-700；化合物 T26521CPMM；CPMM
ABP-700 is a positive allosteric modulator of the GABAA receptor.
价 格：￥电议型 号：T26521产 地：中国大陆
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T26469LA-176120 ammonium；A-176120 铵盐A-176120 ammonium （185049-54-1 Free base）；A-176120 ammonium （185049-54-
A-176120 ammonium is a novel farnesyl pyrophosphate analog with antitumor and antiangiogenic properties and inhibits farnesyltransferase activity.
价 格：￥电议型 号：T26469L产 地：中国大陆
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T26277Tilarginine；化合物 T26277omega-N-Methylarginine|||N-Methylarginine|||L-NMMA|||546C88；omega-N-Methylargi
Tilarginine is a nitric oxide synthetase competitive inhibitor.
价 格：￥电议型 号：T26277产 地：中国大陆
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T26103RMM-46；化合物 T26103RMM-46
RMM-46 is a reversible and selective covalent inhibitor for MSK/RSK-family kinases.
价 格：￥电议型 号：T26103产 地：中国大陆
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T25912Oxypyrronium bromide；化合物 T25912L.D. 3055|||Immetropan|||LD 3055|||LD3055|||LD-3055；L.D. 3055|||Immet
Oxypyrronium bromide is an anticholinergic and spasmolytic agent containing quaternary ammonium. In animal models it inhibited gastric motility, hypotension induced by vagus stimulation or intravenation of acetylcholine; salivation induced by chorda tympani nerve stimulation, and contraction elicited by preganglionic cervical sympathetic nerve stimulation.
价 格：￥电议型 号：T25912产 地：中国大陆
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T258827-O-Demethyl rapamycin；化合物 T25882CJ 12263|||CJ12263|||7-O-Demethyl Rapammune|||Novolimus (80%)|||7-O
Novolimus is a macrocyclic lactone with anti-proliferative properties. It has similar efficacy to currently available agents but requires a lower dose.
价 格：￥电议型 号：T25882产 地：中国大陆
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T25826MMV024101；化合物 T25826MMV-024101|||TCMDC 134293|||TCMDC134293|||TCMDC-134293|||MMV 024101；MMV-024101||
MMV024101 is a PI4K inhibitor. MMV024101 exhibits submicromolar potency against P. falciparum NF54 (IC50 =543 nM), low aqueous solubility (<5 μM), and rapid clearance by mouse liver microsomes with only 2% of parent compound remaining after 30 min of incubation.
价 格：￥电议型 号：T25826产 地：中国大陆
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T25593Labetuzumab govitecan；化合物 T25593IMMU-130|||Labetuzumab-SN38|||hMN14-SN38|||IMMU130|||IMMU 130；IMMU-1
Labetuzumab govitecan is an anti-CEACAM5/SN-38 antibody-drug conjugate for therapy of refractory or relapsing metastatic colorectal cancer.
价 格：￥电议型 号：T25593产 地：中国大陆
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T25530IMM-02；化合物 T25530IMM 02；IMM 02
IMM-02 is a DID-DAD binding inhibitor.
价 格：￥电议型 号：T25530产 地：中国大陆
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T25529IMM-01；化合物IMM-01IMM-01
IMM-01 is a novel class of small-molecule agonists of the mammalian Diaphanous (mDia)-related formins, which act downstream of Rho GTPases to assemble actin filaments, and their organization with microfilaments to establish and maintain cell polarity during migration and asymmetric division. GTP-bound Rho activates mDia family members by disrupting the interaction between the DID and DAD autoregulatory domains, which releases the FH2 domain to modulate actin and microtubule dynamics[1].
价 格：￥电议型 号：T25529产 地：中国大陆
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T25444gamma-Kainylglutamic acid；化合物 T25444gamma-Kan-glu；gamma-Kan-glu
gamma-Kainylglutamic acid is a selective amino acid-induced neuroexcitation antagonist.
价 格：￥电议型 号：T25444产 地：中国大陆
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T25420FK 33-824；化合物 T25420FK-33-824|||Sandoz FK 33-824|||FK33-824|||SAN 33-824|||Damme；FK-33-824|||Sandoz
FK 33-824 ,with similar actions to those of methionine enkephalin(ENKEPHALIN, METHIONINE),is a stable synthetic analog of that. Its effects can be reversed by narcotic antagonists such as naloxone.
价 格：￥电议型 号：T25420产 地：中国大陆
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T25227CFMMC；化合物 T25227CFMMC
CFMMC is an allosteric mGluR1 antagonist agent.
价 格：￥电议型 号：T25227产 地：中国大陆
