9月
SPDP-PEG4-acid；化合物 T16916SPDP-PEG4-acid (2024/9/1)
简介：spdp-peg4-acid 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-C6-NHS ester；化合物 T16915SPDP-C6-NHS ester (2024/9/1)
简介：spdp-c6-nhs ester is an alkyl/ether-based linker utilized in the synthesis of protacs[1].
SP187；化合物SP187UV4|||MON-DNJ；UV4|||MON-DNJ (2024/9/1)
简介：sp187 (mon-dnj) is a host-targeted iminosugar. it has anti-filovirus infection activity.sp187 is used for therapeutic use against influenza and dengue viruses.
Sotirimod；索替莫德R850|||S-30594；R850|||S-30594 (2024/9/1)
简介：sotirimod（r850） is a novel immunomodulator with antitumor and antiviral activity for the study of actinic keratoses.
HH +LUC人皮肤T淋巴细胞瘤细胞 +LUC (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。
Sortin1化合物 T16912Sortin1|||Sortin-1 (2024/9/1)
简介：sortin1, a chemical genetic-hit compound, specifically induces mislocalization of both soluble and membrane-associated vacuolar markers in plants and yeast.
Sorivudine；索立夫定BV-araU；BV-araU|||索立夫定 (2024/9/1)
简介：sorivudine (bv-arau) has antiviral activity against several viruses including varicella zoster virus, herpes simplex type 1 virus, and epstein-barr virus by interfering with viral dna synthesis.
Sorbinil；索比尼尔Sorbinil (2024/9/1)
简介：sorbinil is an aldose reductase inhibitor. sorbinil plays a therapeutic role in treating diabetes and diabetic complications decreases ar activity and inhibit the polyol pathway.
4-Formylbenzoic acid；对醛基苯甲酸Benzoic acid；对醛基苯甲酸|||Benzoic acid (2024/9/1)
简介：4-formylbenzoic acid (benzoic acid) can be used as an intermediate for medicines, pesticides, and optical brighteners.
Donafenib；多纳非尼Sorafenib (D3)|||Bay 43-9006 (D3)|||Sorafenib-d3；Sorafenib (D3)|||Bay 43-9006 (D3)|||S (2024/9/1)
简介：donafenib (bay 43-9006 (d3)) is a deuterium-labeled sorafenib which is a multikinase inhibitor(ic50s: 6 nm, 20 nm, and 22 nm for raf-1, b-raf, and vegfr-3, respectively).
Soluflazine；化合物 T16907Soluflazine (2024/9/1)
简介：soluflazine is a nucleoside transport inhibitor. it also has anticonvulsant action.
HH +LUC+RFP人皮肤T淋巴细胞瘤细胞 +LUC+RFP (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。
Sograzepide；化合物 T16906YM-220|||Netazepide|||YF 476；YM-220|||Netazepide|||YF 476 (2024/9/1)
简介：sograzepide is an effective and highly selective gastrin/cck-b antagonist (ic50: 0.1 nm), has an inhibitory effect on gastrin/cck-a activity (ic50: 502 nm). sograzepide replaces the specific binding of [125i]cck-8 to the rat brain, cloned canine, and cloned human gastrin/cck-b receptors (ki: 0.068, 0.62 and 0.19 nm, respectively).
HH +LUC+RFP人皮肤T淋巴细胞瘤细胞 +LUC+RFP (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。
SNIPER(BRD)-1；化合物 T16905SNIPER(BRD)-1 (2024/9/1)
简介：sniper(brd)-1 is a chemical compound composed of a derivative of the iap antagonist lcl-161 and the bet inhibitor (+)-jq-1, linked together. it promotes the degradation of brd4 through the ubiquitin-proteasome pathway and effectively degrades ciap1, ciap2, and xiap with ic50 values of 6.8 nm, 17 nm, and 49nm, respectively[1].
Smurf1-IN-A01；化合物Smurf1-IN-A01A01；A01 (2024/9/1)
简介：smurf1-in-a01 (a01) is a ubiquitin ligase smad ubiquitination regulatory factor-1 inhibitor (kd: 3.664 nm). it increases bmp-2 responsiveness by inhibiting smurf1-mediated smad1/5 degradation.
SMPH Crosslinker；化合物 T16903SMPH Crosslinker (2024/9/1)
简介：smph crosslinker is an alkyl/ether-based protac linker utilized for synthesizing protacs[1].
SMIP004；化合物SMIP004SMIP004 (2024/9/1)
简介：smip004 is an skp2 e3 ligase inhibitor. smip004 is a cancer cell-selective apoptosis inducer of human prostate cancer cells.
SMER18；化合物 T16900SMER18 (2024/9/1)
简介：smer18 is a small molecule enhancer of rapamycin which acts as an mtor-independent autophagy inducer.
BroMhexine IMpurity B；盐酸氨溴索杂质标准品EBroMhexine IMpurity B (2024/9/1)
简介：bromhexine impurity b reagent used in the preparation of ambroxol and bromhexine (b678600) metabolites ambroxol ep impurity e.
SMCC-DM1；化合物SMCC-DM1DM1-SMCC；DM1-SMCC (2024/9/1)
简介：smcc-dm1 (dm1-smcc) (dm1-smcc) is a drug-linker conjugate which composed of a potent microtubule-disrupting agent dm1 and a linker smcc to make antibody-drug conjugate (adc).
HH +LUC+GFP人皮肤T淋巴细胞瘤细胞 +LUC+GFP (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。
SM-6586；化合物SM-6586SM-6586 (2024/9/1)
简介：sm-6586 is a potent calcium channel antagonist with inhibitory effects on na+/h+ and na+/ca2+ exchange channels, and can be used in the study of cerebrovascular disease and hypertension, among other diseases.
SL 0101-1；化合物SL 0101-1SL0101；SL0101 (2024/9/1)
简介：sl 0101-1 (sl0101) is a selective, efficient, reversible and atp-competitive inhibitor of p90 ribosomal s6 kinase (rsk) that can permeate cell membranes, with an ic50 value of 89 nm for rsk.sl 0101-1 (sl0101) is also a potent rsk1/2 inhibitor with a ki value of 1 μm. sl 0101-1 (sl0101) is also a potent rsk1/2 inhibitor with a ki value of 1 μm.
SL910102；化合物 T16895SL910102 (2024/9/1)
简介：sl910102 is a nonpeptide angiotensin antagonist of the at1 receptor.
SKF96067；化合物 T16894SKF96067 (2024/9/1)
简介：skf96067 is a reversible gastric h+/k+-atpase inhibitor.
SKF-82958；化合物 T16893Chloro-AP|||(±)-SKF 82958；Chloro-AP|||(±)-SKF 82958 (2024/9/1)
简介：skf 82958 is a d1/d5 receptor full agonist.
SKF-82958 hydrobromide化合物 T16892(±)-SKF 82958 hydrobromide|||Chloro-APB hydrobromide (2024/9/1)
简介：skf-82958 hydrobromide is a d1/d5 receptor full agonist.
Toledo人弥漫性大B细胞淋巴瘤细胞 (2024/9/1)
简介：细胞特性种属: 人源组织来源: 外周血疾病: 弥漫性大 b 细胞淋巴瘤年龄: 成人性别: 女细胞类型： 淋巴细胞生长特性: 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。
SKA-121；化合物 T16891SKA-121 (2024/9/1)
简介：ska-121 is a selective kca3.1 activator (ec50s: 109 nm and 4.4 μm for kca3.1 and kca2.3, respectively).
MSN交谈
