9月
Stigmastanol；豆甾烷醇Stigmastanol (2024/9/1)
简介：stigmastanol is a phytosterol isolated from hypericum riparium, which is a cameroonian medicinal plant.
Sterigmatocystine；化合物 T16942Sterigmatocystine (2024/9/1)
简介：sterigmatocystine is an inhibitor of g1 phase and dna synthesis and is used to inhibit p21 activity. sterigmatocystine is a precursor of aflatoxins and a mycotoxin produced by common mold strains from aspergillus versicolor.
Stauprimide；化合物 T16941Stauprimide (2024/9/1)
简介：stauprimide is a non-broad spectrum inhibitor that binds to the myc transcription factor nme2 and blocks its nuclear localization in escs, which causes down-regulation of myc transcription.
STAT5-IN-2；化合物STAT5-IN-2STAT5-IN-2 (2024/9/1)
简介：stat5-in-2 is an inhibitor of stat5 with antileukemic effects (ec50s: 9 μm and 5 μm in k562 and ku812 cells, respectively).
Oxypurinol；羟基嘌呤Oxipurinol；Oxipurinol|||羟基嘌呤 (2024/9/1)
简介：oxypurinol is a xanthine oxidase inhibitor. oxipurinol is potentially used for the treatment of congestive heart failure.
Stains-All；着色剂-ALLStains-All (2024/9/1)
简介：stains-all is a cationic dye of carbocyanine.
HUG1-N +LUC+RFP人胃肾小管腺癌+LUC+RFP (2024/9/1)
简介：细胞特性种属: 人源组织来源: 腹水疾病: 胃管状腺癌年龄: 55岁性别: 男细胞类型: 淋巴细胞样生长特性: 悬浮生长含量：>1x10^6 细胞数规格：t25瓶或者1ml冻存管包装用途：仅供科研使用。
ST034307；化合物ST034307ST034307 (2024/9/1)
简介：st034307 is an effective and selective inhibitor of adenylyl cyclase 1 (ic50: 2.3 μm).
ST 2825；化合物 T16937ST 2825 (2024/9/1)
简介：st 2825 is a specific myd88 dimerization inhibitor. st2825 inhibition of il-1β-mediated activation of nf-κb transcriptional activity.
SS-208；化合物SS-208SS-208 (2024/9/1)
简介：ss-208 is a selective inhibitor of hdac6 (ic50 = 12 nm) with anti-tumor activity. ss-208 shows selectivity over other hdac subtypes.
SRX246；化合物 T16934SRX246 (2024/9/1)
简介：srx246 has no interaction at v1b and v2 receptors. srx246 shows negligible binding at 64 other receptors classes, including 35 g-proteincoupled receptors. srx246 is a potent and cns-penetrant vasopressin 1a (v1a) receptor antagonist (ki=0.3 nm for human v1a).
SRT3190；化合物 T16933SRT3190 (2024/9/1)
简介：srt3190 is an antagonist of cxcr2.
SRT 2183；化合物SRT 2183SRT 2183 (2024/9/1)
简介：srt 2183 is a selective activator of sirtuin-1 (sirt1, ec1.5 : 0.36 μm).
SR9238；化合物SR9238SR9238 (2024/9/1)
简介：sr9238 is a synthetic agonist of liver x receptor inverse (ic50s: 214 nm and 43 nm for lxrα and lxrβ, respectively).
Umbelliferone；7-羟基香豆素Skimmetine|||Hydrangin|||Hydrangine|||7-Hydroxycoumarin|||NSC 19790；Skimmetine| (2024/9/1)
简介：umbelliferone (7-hydroxycoumarin) is found in anise. umbelliferone occurs widely in plants including angelica species phytoalexin of infected sweet potat. it has been reported to have antioxidant properties.
SR2211；化合物SR2211SR2211 (2024/9/1)
简介：sr2211 is a specific modulator and an inverse agonist of rorγ(ic50 = 320 nm, ki = 105 nm).
HUG1-N +LUC+GFP人胃肾小管腺癌+LUC+GFP (2024/9/1)
简介：细胞特性种属: 人源组织来源: 腹水疾病: 胃管状腺癌年龄: 55岁性别: 男细胞类型: 淋巴细胞样生长特性: 悬浮生长含量：>1x10^6 细胞数规格：t25瓶或者1ml冻存管包装用途：仅供科研使用。
SR-3306；化合物SR-3306SR-3306 (2024/9/1)
简介：sr-3306 is a potent and highly inhibitor of brain penetrant jnk.
SR-31747；化合物 T16926SR-31747 (2024/9/1)
简介：sr-31747 blocks cell proliferation by inhibiting sterol isomerase. sr-31747 is a sigma ligand. it has immunosuppressive and anti-inflammatory properties.
HUG1-N +LUC+GFP人胃肾小管腺癌+LUC+GFP (2024/9/1)
简介：细胞特性种属: 人源组织来源: 腹水疾病: 胃管状腺癌年龄: 55岁性别: 男细胞类型: 淋巴细胞样生长特性: 悬浮生长含量：>1x10^6 细胞数规格：t25瓶或者1ml冻存管包装用途：仅供科研使用。
SQ109；化合物SQ109NSC 722041；NSC 722041 (2024/9/1)
简介：sq109 (nsc-722041) is an effective inhibitor of the trypomastigote form of the parasite (ic50 = 50 nm). sq109 is an antitubercular agent and targets mmpl3.
SPR inhibitor 3化合物 T16924SPRi3 (2024/9/1)
简介：spr inhibitor 3 is an effective sepiapterin reductase inhibitor. spr inhibitor 3 decreases neuropathic and inflammatory pain through a reduction of bh4 levels. spr inhibitor 3 shows a high binding affinity to human spr in a cell-free assay (ic50=74 nm) and efficiently reduces biopterin levels in a cell-based assay (ic50=5.2 μm).
SPP-86；化合物SPP-86SPP-86 (2024/9/1)
简介：spp-86 is an effective and selective cell-permeable inhibitor of ret tyrosine kinase with an ic50 of 8 nm.
SPL-707；化合物 T16921SPL-707 (2024/9/1)
简介：spl-707 is an effective and selective signal peptide peptidase-like 2a inhibitor (ic50: 80 nm).
SPK-601；化合物 T16920LMV-601；LMV-601 (2024/9/1)
简介：spk-601 is an inhibitor of phosphatidylcholine-specific phospholipase c.
3-(3,4-Dimethoxyphenyl)propanoic acid；3-(3,4-二甲氧基苯)丙酸3,4-Dimethoxyhydrocinnamic acid；3,4-Dimethoxyhy (2024/9/1)
简介：3-(3,4-dimethoxyphenyl)propanoic acid (3,4-dimethoxyhydrocinnamic acid) is an orally active short-chain fatty acid (scfas). it promotes γ-globin gene expression and erythropoiesis in vivo and can be used in beta hemoglobinopathies and other anemias.
HH 人皮肤T淋巴细胞瘤细胞 (2024/9/1)
简介：细胞特性种属: 人源组织来源: 外周血疾病: 淋巴瘤年龄: 61岁性别: 男细胞类型: 淋巴母细胞生长特性: 悬浮生长含量：>1x10^6 细胞数规格：t25瓶或者1ml冻存管包装用途：仅供科研使用。
Spirendolol；化合物 T16919S 32-468|||Substance 32468|||Li 32-468；S 32-468|||Substance 32468|||Li 32-468 (2024/9/1)
简介：spirendolol is an antagonist of β adrenergic receptor.
SPDP-PEG6-NHS ester；化合物 T16918SPDP-PEG6-NHS ester (2024/9/1)
简介：spdp-peg6-nhs ester is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
SPDP-PEG4-NHS ester；化合物 T16917SPDP-PEG4-NHS ester (2024/9/1)
简介：spdp-peg4-nhs ester is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
MSN交谈
