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CYTOCHALASINP

更新时间:2026-08-03 05:14:55

CYTOCHALASINP结构式
CYTOCHALASINP结构式
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常用名 CYTOCHALASINP 英文名 CYTOCHALASINP
CAS号 108050-27-7 分子量 511.65000
密度 1.23g/cm3 沸点 678.9ºC at 760mmHg
分子式 C30H41NO6 熔点 N/A
MSDS N/A 闪点 N/A

 CYTOCHALASINP名称

英文名 Cytochalasin Ppho

 CYTOCHALASINP物理化学性质

密度 1.23g/cm3
沸点 678.9ºC at 760mmHg
分子式 C30H41NO6
分子量 511.65000
精确质量 511.29300
PSA 119.58000
LogP 3.20880
InChIKey AVASIWUXPVFFGK-WRERFMELSA-N
SMILES CC(=O)OC1C=CC(C)(O)CC(C)CC=CC2C(O)C(C)(O)C(C)C3C(Cc4ccccc4)NC(=O)C123
蒸汽压 2.34E-19mmHg at 25°C
折射率 1.597

 CYTOCHALASINP上下游产品

CYTOCHALASINP上游产品  1

CYTOCHALASINP下游产品  0

 CYTOCHALASINP靶点实验

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实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
实验名称:Primary cell-based high-throughput screening for identification of compounds that all...
来源:Johns Hopkins Ion Channel Center
靶标:MAS-related GPR member X1 [Homo sapiens]
External Id:JHICC_MrgX1_AlloAgonist_Primary
实验名称:Primary cell-based high-throughput screening for identification of compounds that ant...
来源:Johns Hopkins Ion Channel Center
靶标:MAS-related GPR member X1 [Homo sapiens]
External Id:JHICC_MrgX1_Antagonist_Primary
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
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