当前位置：易推广 > 上海陶术生物科技有限公司 > 产品展示
企业档案
会员类型：会员
已获得易推广信誉 等级评定
(0 -40)基础信誉积累，可浏览访问
(41-90)良好信誉积累，可接洽商谈
(91+ )优质信誉积累，可持续信赖
易推广会员：5年
工商认证 【已认证】
最后认证时间：
注册号： 【已认证】
法人代表： 【已认证】
企业类型：生产商 【已认证】
注册资金：人民币万 【已认证】
产品数：86101
参观次数：3877920
自主品牌
已选条件
-
T16283Neocarzinostatin；化合物 T16283Neocarzinostatin
Neocarzinostatin is an effective DNA-damaging, anti-tumor antibiotic. It recognizes double-stranded DNA bulge and induces DNA double strand breaks (DSBs). Neocarzinostatin leads to apoptosis. Neocarzinostatin has potential for EpCAM-positive cancer treatment.
价 格：￥电议型 号：T16283产 地：中国大陆
-
T1628Rivastigmine tartrate；酒石酸卡巴拉汀SDZ-ENA 713|||ENA 713；SDZ-ENA 713|||ENA 713|||酒石酸卡巴拉汀
Rivastigmine tartrate (SDZ-ENA 713) is a carbamate-derived reversible CHOLINESTERASE INHIBITOR that is selective for the CENTRAL NERVOUS SYSTEM and is used for the treatment of DEMENTIA in ALZHEIMER DISEASE and PARKINSON DISEASE.
价 格：￥电议型 号：T1628产 地：中国大陆
-
T16273Napsagatran hydrate；化合物 T16273Ro 46-6240/010 hydrate|||Ro 46-6240 hydrate；Ro 46-6240/010 hydrate|||R
Napsagatran hydrate is a novel and specific inhibitor of thrombin.
价 格：￥电议型 号：T16273产 地：中国大陆
-
T16270Nanatinostat；化合物 T16270CHR-3996；CHR-3996
Nanatinostat is an effective and class I selective inhibitor of histone deacetylase (IC50: 8 nM).
价 格：￥电议型 号：T16270产 地：中国大陆
-
T16262N33-TEG-COOH；化合物 T1626214-Azido-3,6,9,12-tetraoxatetradecanoic acid|||N3-TEG-COOH；14-Azido-3,6,9,12-
N33-TEG-COOH 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.
价 格：￥电议型 号：T16262产 地：中国大陆
-
T16251N-Succinimidyl-S-acetylthioacetate；N-丁二酸，S-乙酰基巯基乙二醇酯SATA；SATA|||N-丁二酸，S-乙酰基巯基乙二醇酯
N-Succinimidyl-S-acetylthioacetate (SATA) is a protein modification agent that introduces thiol-groups into protein molecules and adds sulfhydryl groups in a protected form to proteins and other amine-containing molecules for later reaction with sulfhydryl reactive crosslinkers such as Sulfo-SMCC, Sulfo-MBS, etc.
价 格：￥电议型 号：T16251产 地：中国大陆
-
T16250N-Succinimidyl 3-(Bromoacetamido)propionate；化合物 T162503-(2-Bromoacetamido)propanoic acid NHS ester；3
N-Succinimidyl 3-(Bromoacetamido)propionate is a PEG-based PROTAC linker employed in the synthesis of PROTACs and antibody-drug conjugates (ADCs) [1, 2]. It acts as a cleavable ADC linker, facilitating the conjugation of drugs to antibodies for targeted delivery [2].
价 格：￥电议型 号：T16250产 地：中国大陆
-
T16239N-Methylisatoic anhydride；N-甲基靛红酸酐NMIA；NMIA|||N-甲基靛红酸酐|||1-甲基苯唑
N-Methylisatoic anhydride is a 2´-OH selective acylation agent of RNAs. It is also widely used for resolving secondary RNA structures using the SHAPE technology.
价 格：￥电议型 号：T16239产 地：中国大陆
-
T1622Rosiglitazone maleate；马来酸罗格列酮BRL 49653C|||BRL 49653；BRL 49653C|||BRL 49653|||马来酸罗格列酮
Rosiglitazone maleate (BRL 49653) is the maleate salt of rosiglitazone, an orally-active thiazolidinedione with antidiabetic properties and potential antineoplastic activity.
价 格：￥电议型 号：T1622产 地：中国大陆
-
T1621Imatinib Mesylate；甲磺酸伊马替尼ST-1571 Mesylate|||STI-571|||CGP-57148B；甲磺酸伊马替尼|||ST-1571 Mesylate|||STI-57
Imatinib Mesylate (STI571 Mesylate) is a multi-targeted receptor tyrosine kinase inhibitor that selectively inhibits the kinase activities of BCR/ABL, v-Abl, PDGFR, and c-kit with oral activity. Imatinib Mesylate has antitumor activity for the treatment of chronic granulocytic leukemia.
价 格：￥电议型 号：T1621产 地：中国大陆
-
T1620Pazufloxacin Mesylate；帕珠沙星甲磺酸盐Pazucross|||Pazufloxacin mesilate|||T-3762|||Pazufloxacin methanesulfo
Pazufloxacin Mesylate (T-3762) is a fluoroquinolone antibiotic.
价 格：￥电议型 号：T1620产 地：中国大陆
-
T16162Mutated EGFR-IN-1；AZD9291中间体1Osimertinib analog；Osimertinib analog|||AZD9291中间体1
Mutated EGFR-IN-1 (Osimertinib analog) is a useful intermediate for the inhibitors design for mutated EGFR, such as L858R EGFR, Exonl9 deletion activating mutant, and T790M resistance mutant.
价 格：￥电议型 号：T16162产 地：中国大陆
-
T16152Betamethasone 17-benzoate；苯甲酸倍他米松Betamethasone 17-benzoate
Betamethasone 17-benzoate is a representative steroid. It also can be used in the treatment of recurrent aphothous ulcers (RAU).
价 格：￥电议型 号：T16152产 地：中国大陆
-
T16122MMAF sodium；化合物 T16122Monomethylauristatin F sodium；Monomethylauristatin F sodium
MMAF sodium is widely used as a cytotoxic component of antibody-drug conjugates (ADCs) such as Vorsetuzumab mafodotin and SGN-CD19A. MMAF sodium is an effective tubulin polymerization inhibitor and is used as an antitumor agent.
价 格：￥电议型 号：T16122产 地：中国大陆
-
T16121MMAF Hydrochloride；化合物 T16121Monomethylauristatin F Hydrochloride；Monomethylauristatin F Hydrochlori
MMAF Hydrochloride is widely used as a cytotoxic component of antibody-drug conjugates (ADCs) such as Vorsetuzumab mafodotin and SGN-CD19A. MMAF Hydrochloride is an effective tubulin polymerization inhibitor and is used as an antitumor compound.
价 格：￥电议型 号：T16121产 地：中国大陆
-
T1612Neostigmine methyl sulfate；甲硫酸新斯的明Normastigmin|||Hodostin|||Syntostigmin；Normastigmin|||甲基硫酸新斯的明|||甲
Neostigmine methyl sulfate (Syntostigmin) is a reversible inhibitor of acetylcholinesterase, can not cross the blood-brain barrier, used in the treatment of myasthenia gravis.
价 格：￥电议型 号：T1612产 地：中国大陆
-
T16117Pevonedistat hydrochloride化合物 T16117MLN4924 hydrochloride
Pevonedistat hydrochloride is an effective and selective inhibitor of NEDD8-activating enzyme (IC50: 4.7 nM).
价 格：￥电议型 号：T16117产 地：中国大陆
-
T16098Islatravir；化合物IslatravirMK-8591；MK-8591
Islatravir (MK-8591) is an effective anti-HIV-1 agent. It acts as a nucleoside reverse transcriptase inhibitor (EC50s: 0.068 nM, 3.1 nM, and 0.15 nM for HIV-1 (WT), HIV-1 (M184V), HIV-1 (MDR), respectively).
价 格：￥电议型 号：T16098产 地：中国大陆
-
T16091MK-0812 Succinate；化合物MK-0812 SuccinateMK-0812 Succinate
MK-0812 Succinate is an effective and selective CCR2 antagonist.
价 格：￥电议型 号：T16091产 地：中国大陆
-
T16082Mivotilate；化合物 T16082YH439；YH439
Mivotilate, a potent, non-toxic aryl hydrocarbon receptor (AhR) activator, functions as a hepatoprotective agent.
价 格：￥电议型 号：T16082产 地：中国大陆
