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T28297Parsaclisib hydrochloride；化合物Parsaclisib HClParsaclisib HCl|||INCB-50465|||INCB 050465|||INCB-050465
Parsaclisib hydrochloride (INCB050465 HCl) is a selectve PI3Kδ inhibitor with antitumor activity. Parsaclisib demonstrates potent activity with IC50 values ranging from 0.2 to 2 nM.
价 格：￥电议型 号：T28297产 地：中国大陆
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T28197NS-2710；化合物 NS-2710NS 2710|||NS2710；NS 2710|||NS2710
NS-2710 is a non-selective GABA(A) receptor partial agonist for the study of anxiety disorders.
价 格：￥电议型 号：T28197产 地：中国大陆
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T28098MRS1097；化合物 T28098MRS-1097|||MRS 1097；MRS-1097|||MRS 1097
MRS1097 is a selective antagonist A3 adenosine receptor.
价 格：￥电议型 号：T28098产 地：中国大陆
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T28097MRS1067；化合物 T28097MRS 1067|||MRS-1067；MRS 1067|||MRS-1067
MRS1067 is an antagonist of A3 adenosine receptor.
价 格：￥电议型 号：T28097产 地：中国大陆
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T28072LMLN-3897 TFA；MLN-3897三氟乙酸盐MLN-3897 TFA(1010731-97-1 Free base)；MLN-3897 TFA(1010731-97-1 Free base)
MLN-3897 TFA is a potent CCR1 antagonist that inhibits the binding of 125I-MIP-1α to THP-1 cell membranes.
价 格：￥电议型 号：T28072L产 地：中国大陆
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T28072MLN-3897；化合物MLN-3897AVE9897|||AVE 9897|||CCR1 antagonist 10|||AVE-9897；AVE9897|||AVE 9897|||CCR1 ant
MLN-3897 (CCR1 antagonist 10) is an orally active antagonist of CCR1 with a Ki of 2.3 nM for 125I-MIP-1α binding to THP-1 cell membranes. MLN-3897 inhibits Akt signaling and MM cell survival and proliferation.
价 格：￥电议型 号：T28072产 地：中国大陆
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T28000MDK49781；化合物 T28000MDK-49781|||MDK 49781；MDK-49781|||MDK 49781
MDK49781 is a useful chemical intermediate for drug synthesis.
价 格：￥电议型 号：T28000产 地：中国大陆
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T27997MDK-3345；化合物 T27997MDK 3345|||Mcl-1 Inhibitor11|||Mcl-1 Inhibitor 11|||Mcl-1 Inhibitor-11；MDK 3345||
MDK-3345 is a reversible covalent inhibitor for Mcl-1.
价 格：￥电议型 号：T27997产 地：中国大陆
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T27979Masilukast；马鲁司特ICI-D-3523|||ZD-3523|||ICI D-3523|||MCC-847|||SA-09012|||D-3523；ICI-D-3523|||ZD-3523|
Masilukast(MCC-847) is an oral leukotriene D4 (LTD4) receptor antagonist for the study of diseases associated with inflammation.
价 格：￥电议型 号：T27979产 地：中国大陆
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T27978Maritinone；化合物 T27978Maritinone
Maritinone is a novel anti-tuberculosis (anti-TB) agent.
价 格：￥电议型 号：T27978产 地：中国大陆
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T27977Manzamine A；化合物 T27977Keramamine A；Keramamine A
Manzamine A is a GSK-3 inhibitor and vacuolar ATPase uncoupler found in marine sponges. It inhibits autophagy and tumor growth in cancer models, suppresses foam cell formation in macrophages, prevents growth of gram negative and gram positive bacteria, and decreases tau hyperphosphorylation.
价 格：￥电议型 号：T27977产 地：中国大陆
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T27976Manifaxine；化合物 T27976BW1555U88|||BW-1555U-88|||1555U88|||1555U-88|||GW-320659|||GW320659；BW1555U88||
Manifaxine, a norepinephrine-dopamine reuptake inhibitor, is used potentially for the treatment of attention deficit.
价 格：￥电议型 号：T27976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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T27974Maleimide-PEG4-NHS；化合物 T27974MAL-PEG-NHS|||Maleimide PEG NHS|||Maleimido-?Tetra(Ethylene Glycol)?-?A
Maleimide-PEG4-NHS is a sulfhydryl and amine reactive heterofuncational PEG linker. The chemical bonds formed through Maleimide-PEG4-NHS linker are stable and are not cleavable. The NHS ester reacts with amino groups at pH 7-9 to form stable amide bond while maleimide reacts with thiol groups at pH 6.5-7.5 to form stable thiol-ether bond.
价 格：￥电议型 号：T27974产 地：中国大陆
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T27973MAIM1；化合物 T27973MAIM1
MAIM1 selectively inhibits MCL-1deltaNdeltaC binding activity.
价 格：￥电议型 号：T27973产 地：中国大陆
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T27972MAC173979；化合物 T27972MAC-173979|||MAC 173979；MAC-173979|||MAC 173979
MAC173979 inhibits E. coli de novo PABA biosynthesis and growth.
价 格：￥电议型 号：T27972产 地：中国大陆
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T27971MAC-0547630；化合物 T27971MAC 0547630；MAC 0547630
MAC-0547630 potent and selective inhibitor of UppS.
价 格：￥电议型 号：T27971产 地：中国大陆
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T27970Mabuterol free base；化合物 T27970Mabuterol|||PB 868Cl；Mabuterol|||PB 868Cl
Mabuterol is a selective agonist of β2 adrenoreceptor with no beta 1-stimulation. Mabuterol inhibited the positive inotropic effect of isoprenaline at 10(-7) g/ml and decreased the maximum driving frequency at 3 X 10(-6) g/ml. Mabuterol was 3 times more potent in relaxing the isolated rat uterus, but 700 times less potent than isoprenaline in relaxing the rabbit jejunum. Mabuterol (p.o.) depressed the intestinal propulsion and was equipotent to isoprenaline and 2.5 times less potent than salbuta
价 格：￥电议型 号：T27970产 地：中国大陆
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T2797Harmaline；哈马灵Harmaline
Harmaline is a fluorescent psychoactive indole alkaloid from the group of harmala alkaloids and beta-carbolines. It is the reduced hydrogenated form of harmine.
价 格：￥电议型 号：T2797产 地：中国大陆
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T27950LY389795；化合物 T27950LY-389795|||LY 389795；LY-389795|||LY 389795
LY389795 is an agonist of group II (mGlu2/3) metabotropic glutamate receptor, it is used in inflammatory pain models.
价 格：￥电议型 号：T27950产 地：中国大陆
