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T9902AtezolizumabAtezolizumab,Inhibitor,MPDL3280A,inhibit,Apoptosis,Autophagy
Atezolizumab anti-PD-L1) is a fully humanized IgG1 monoclonal antibody that blocks the interaction of PD-L1 with both PD-1 and B7.1 but not the interaction of PD-L2 with PD-1.
价 格：￥电议型 号：T9902产 地：中国大陆
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T40732TMPD dihydrochloridedonor,Cytochrome-c,TMPD dihydrochloride,redox,inhibit,electron,enzymatically,blu
TMPD dihydrochloride is an active substrate of enzymatically convert redox and an electron donor for the reduction of heme peroxidases.
价 格：￥电议型 号：T40732产 地：中国大陆
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T24850Takeda103ACMPD103A；Takeda-103A；CMPD-103A；Takeda 103 A；Takeda-103-A
Takeda103A is the GRK2-dependent bovine tubulin oxidation effective inhibitor.
价 格：￥电议型 号：T24850产 地：中国大陆
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T14989CMPD101
CMPD101 is a membrane-permeable small-molecule inhibitor of GRK2/3 (IC50: 18 nM and 5.4 nM). Which can be used for the study of heart failure. CMPD101 exhibits less selectively against GRK1, GRK5, ROCK-2 and PKCα with IC50s of 3.1 μM , 2.3 μM, 1.4 μM and
价 格：￥电议型 号：T14989产 地：中国大陆
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T14988CMPD1
CMPD1 is a non-ATP-competitive p38 MAPK-mediated MK2 phosphorylation inhibitor(apparent Ki (Kiapp): 330?nM).
价 格：￥电议型 号：T14988产 地：中国大陆
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T14565BI-671800Cmpd A；AP-761
BI-671800 is a highly specific and potent antagonist of chemoattractant receptor-homologous molecule on Th2 cells (DP2/CRTH2). With IC50 values of 4.5 nM and 3.7 nM for PGD2 binding to CRTH2 in hCRTH2 and mCRTH2 transfected cells, respectively. BI-671800
价 格：￥电议型 号：T14565产 地：中国大陆
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T0763Hexylene glycol己二醇；已二醇；2-Methyl-2,4-pentanediol；Diolane；MPD
Diolane, colorless liquid, is a chiral diol. It is an industrial compound produced from diacetone alcohol by hydrogenation.
价 格：￥电议型 号：T0763产 地：中国大陆
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T0763DiolaneDiolane,MPD,2-Methyl-2,4-pentanediol
Diolane, colorless liquid, is a chiral diol. It is an industrial compound produced from diacetone alcohol by hydrogenation.
价 格：￥电议型 号：T0763产 地：美洲
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T12099MPDCMPDC
MPDC is a competitive inhibitor of the Na+-dependent high-affinity glutamate transporter in forebrain synaptosomes.
价 格：￥电议型 号：T12099产 地：美洲
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T82702CMPD167；化合物 CMPD167MRK-1；MRK-1
CMPD167 (MRK-1) is a potent, orally active inhibitor of CCR5 with significant in vitro antiviral efficacy [1].
价 格：￥电议型 号：T82702产 地：中国大陆
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T72917D-threo-PDMP；化合物 D-threo-PDMPD-threo-PDMP
D-threo-PDMP is a potent inhibitor of glucoceramide synthase (GCS), effectively reducing cell surface glycosphingolipids by inhibiting glycosylation. It also decreases the axon plexus´s total length and the number of axon branch points, ultimately inhibiting neurite growth.
价 格：￥电议型 号：T72917产 地：中国大陆
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T72635AMPD2 inhibitor 2；化合物 AMPD2 inhibitor 2AMPD2 inhibitor 2
AMPD2 Inhibitor 2 is a potent inhibitor of AMP deaminase 2 (AMPD2), demonstrating inhibitory concentration 50 (IC50) values of 0.1 μM for human AMPD2 (hAMPD2) and 0.28 μM for mouse AMPD2 (mAMPD2). This compound is valuable for research into the physiological roles of AMPD2, especially in mice on a high-fat diet.
价 格：￥电议型 号：T72635产 地：中国大陆
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T70628Cmpd-A；化合物 Cmpd-ACmpd-A
Cmpd-A is a time-dependent CENP-E inhibitor with potent antitumor activity. Cmpd-A inhibits the ATPase activity of the CENP-E motor domain, acting as a time-dependent inhibitor with an ATP-competitive-like behavior. Cmpd-A causes chromosome misalignment on the metaphase plate, leading to prolonged mitotic arrest. Treatment with Cmpd-A induces antiproliferation in multiple cancer cell lines.
价 格：￥电议型 号：T70628产 地：中国大陆
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T62338IMPDH2-IN-2；化合物 IMPDH2-IN-2IMPDH2-IN-2
IMPDH2-IN-2 is a potent inhibitor of inosine 5´-monophosphate dehydrogenase (IMPDH) (Ki,app: 14 μM) and a potential anti-tuberculosis agent. IMPDH2-IN-2 has a moderate antibacterial effect with MIC values of 6.3 and 11 μM in minimal GAST/Fe and rich 7H9/ADC/Tween media, respectively. μM.
价 格：￥电议型 号：T62338产 地：中国大陆
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T40732TMPD dihydrochloride；四甲基对苯二胺二盐酸盐TMPD dihydrochloride
TMPD dihydrochloride is an active substrate of enzymatically convert redox and an electron donor for the reduction of heme peroxidases.
价 格：￥电议型 号：T40732产 地：中国大陆
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T38822D-threo-PPMP；D-threo-PPMPD-threo-PPMP
D-threo-PPMP, a powerful glucosylceramide (GlcCer) synthase inhibitor, effectively impedes karyokinesis and decreases cyst formation.
价 格：￥电议型 号：T38822产 地：中国大陆
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T38489D,L-erythro-PDMP；D,L-erythro-PDMPD,L-erythro-PDMP
D,L-erythro-PDMP, an erythro isomer of PDMP, exhibits growth inhibition on cultured rabbit skin fibroblasts. Additionally, this compound serves as an effective inhibitor of UDP-glucose: ceramide glucosyltransferase.
价 格：￥电议型 号：T38489产 地：中国大陆
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T33313Methanesulfonic acid, compd. with alpha-(ethylthio)-4-(octyloxy)-m-toluidine (7CI)；化合物 T33313Methane
Methanesulfonic acid, compd. with alpha-(ethylthio)-4-(octyloxy)-m-toluidine (7CI) is a bioactive chemical.
价 格：￥电议型 号：T33313产 地：中国大陆
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T333124-(Octyloxy)-m-toluidine methanesulfonate；化合物 T33312Methanesulfonic acid, compd. with 4-(octyloxy)-m
Methanesulfonic acid, compd. with 4-(octyloxy)-m-toluidine (7CI) is a bioactive chemical.
价 格：￥电议型 号：T33312产 地：中国大陆
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T30905Choline, compd. with 3-butyl-1-ethyl-6-thioxanthine；化合物 T30905Choline, compd. with 3-butyl-1-ethyl-6
Choline, compd. with 3-butyl-1-ethyl-6-thioxanthine is a bioactive chemical.
价 格：￥电议型 号：T30905产 地：中国大陆
