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T69512IHCH7041；化合物 IHCH7041IHCH7041
IHCH7041, also known as (+/-)-IHCH7041, is a DRD2 partial agonist. IHCH7041 contains two enantiomers: (-)-IHCH7041 and (+)-IHCH7041 (optical rotation negative and positive). (+/-)-IHCH7041 has CAS#2813335-29-2. Two isomers have CAS#2813335-07-6 (rotation negative) and 2813335-06-5 (rotation positive), respectively.
价 格：￥电议型 号：T69512产 地：中国大陆
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T6471410× TBS (PH7.4)；化合物 10× TBS (PH7.4)10× TBS (PH7.4)
10× TBS (PH7.4) is a reagent and has a wide range of applications in life science related research.
价 格：￥电议型 号：T64714产 地：中国大陆
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T6066SCH772984；化合物SCH772984SCH772984
SCH 772984 is a potent inhibitor of ERK1/ERK2 (IC50: 4/1 nM) and has only weak inhibitory for other 300 tested kinases.
价 格：￥电议型 号：T6066产 地：中国大陆
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T6060LAnabasine HCl；化合物 T6060LBB-NC-0036|||CCG-38440|||H-8174|||AR-1H7273|||ZX-BK000320|||ST-24041653；BB-N
Anabasine HCl is used as a clinical biomarker for tobacco smoke exposure and as an insecticide. It is also a depolarizing NMJ blocker, aromatase inhibitor, nAChr antagonist, and teratogen found in species of Nicotiana.
价 格：￥电议型 号：T6060L产 地：中国大陆
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T5635CH7057288；化合物CH7057288CH7057288
CH7057288 is an effective and selective TRK inhibitor with an IC50 value of 1.1 nM, 7.8 nM and 5.1 nM for TRKA, TRKB and TRKC, respectively.
价 格：￥电议型 号：T5635产 地：中国大陆
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T3599BFH772化合物BFH772BFH-722
BFH772, a structure analogue of BAW2881, is a potent and selective VEGF inhibitor. BFH772 is highly effective at targeting VEGFR2 kinase with an IC50 value of 3 nM. BFH772 inhibits the ligand induced autophosphorylation of RET, PDGFR, and KIT kinases, with IC50 values ranging between 30 and 160 nM.
价 格：￥电议型 号：T3599产 地：中国大陆
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T35334CH7233163；CH7233163CH7233163
CH7233163 是一种EGFR-tyrosine kinase 的非共价ATP 竞争性抑制剂，对有EGFR-Del19/T790M/C797S 的肿瘤具有抗肿瘤活性。
价 格：￥电议型 号：T35334产 地：中国大陆
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T31076CP-74667 mesylate；化合物 T31076CP 74667 mesylate|||UNII-96Z3H79YX9；CP 74667 mesylate|||UNII-96Z3H79YX9
CP-74667 mesylate is a bio-active chemical.
价 格：￥电议型 号：T31076产 地：中国大陆
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T29738AH 7079；化合物 T29738AH7079|||AH-7079；AH7079|||AH-7079
AH 7079 is a biochemical.
价 格：￥电议型 号：T29738产 地：中国大陆
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T29149VX 759；化合物 T29149VCH759|||BCH27759|||VX-759|||VX759|||VCH-759|||BCH-27759；VCH759|||BCH27759|||VX-759
VX 759, a nonstructural protein 5B (NS5B) inhibitor, is used potentially for the treatment of HCV infection.
价 格：￥电议型 号：T29149产 地：中国大陆
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T28734SCH79797化合物 T28734SCH 79797|||SCH-79797
SCH-79797 is a potent and selective PAR1 antagonist.
价 格：￥电议型 号：T28734产 地：中国大陆
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T26840BMH-7；化合物 T26840BMH7；BMH7
BMH-7 is a p53 activator with potent antitumor activity.
价 格：￥电议型 号：T26840产 地：中国大陆
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T26291Triazamate；化合物 T26291RH-7988|||RH7988|||RH 7988|||Triazuron；RH-7988|||RH7988|||RH 7988|||Triazuron
Triazamate is used as a dimethylcarbamate insecticide.
价 格：￥电议型 号：T26291产 地：中国大陆
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T25481H 77；化合物 T25481H77|||H-77；H77|||H-77
H 77 is a new effective renin inhibitor. H 77 is angiotensinogen (6-13)-octapeptide in which the peptide bond -CO-NH- at the Leu(9)-Leu(11) linkage is replaced by a -CH2-NH- bond.
价 格：￥电议型 号：T25481产 地：中国大陆
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T25475Gyki 32887；化合物 T25475RGH-7825|||Gyki-32887|||Gyki32887|||RGH 7825|||RGH7825；RGH-7825|||Gyki-32887|||
Gyki 32887 is a dopamine agonist.
价 格：￥电议型 号：T25475产 地：中国大陆
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T23671AH 7725；化合物 T23671AH-7725|||AH7725；AH-7725|||AH7725
AH 7725 is an inhibitor of the asthma attack.
价 格：￥电议型 号：T23671产 地：中国大陆
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T23338SCH772984 TFA (942183-80-4 free base)；化合物 T23338SCH772984 TFA；SCH772984 TFA
ERK1/2 inhibitor
价 格：￥电议型 号：T23338产 地：中国大陆
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T23337SCH772984 HCl；化合物SCH772984 HClSCH772984 HCl
SCH772984 HCl is a selective inhibitor of ERK1/2 that displays behaviors of both type I and type II kinase inhibitors, with IC50s of 4 and 1 nM, respectively. SCH772984 HCl has nanomolar cellular potency in tumor cells with mutations in BRAF, NRAS, or KRA
价 格：￥电议型 号：T23337产 地：中国大陆
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T1974PH-797804；化合物PH797804PH797804；PH797804
PH-797804 is a pyridinone inhibitor of p38α (IC50: 26 nM, in a cell-free assay); 4-fold more selective versus p38β and does not inhibit JNK2.
价 格：￥电议型 号：T1974产 地：中国大陆
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T12870SCH79797 dihydrochloride；化合物SCH79797 dihydrochlorideSCH79797 dihydrochloride
SCH79797 dihydrochloride is an effective and selective antagonist of protease activated receptor 1 (PAR1) with an IC50 of 70 nM and a Ki of 35 nM. SCH79797 dihydrochloride has antiproliferative and pro-apoptotic effects.
价 格：￥电议型 号：T12870产 地：中国大陆
