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T21598G3335；化合物 T21598G3335
H- Trp- Glu- OH is a selective, reversible and cell-permeable PPARγ with a K d of ~8 μM, which might be developed as a possible lead compound in diabetes research [1].
价 格：￥电议型 号：T21598产 地：中国大陆
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T21593AAL-993；化合物AAL-993AAL-993
AAL-993 is a potent VEGFR inhibitor with IC50s of 130 nM, 23 nM and 18 nM for VEGFR1, VEGFR2 and VEGFR3, respectively. AAL993 has a weak inhibitory effect on other tyrosine kinases. AAL993 also shows potent antiangiogenic and antitumor activities.
价 格：￥电议型 号：T21593产 地：中国大陆
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T215911H-1-ethyl Candesartan Cilexetil；坎地沙坦酯杂质E1H-1-ethyl Candesartan Cilexetil
1H-1-ethyl Candesartan Cilexetil is a process-related impurity in the bulk synthesis of candesartan cilexetil, which is a potent, long-acting and selective angiotensin II type 1 receptor (AT1) antagonist.
价 格：￥电议型 号：T21591产 地：中国大陆
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T2159CaMKP Inhibitor；化合物CaMKP InhibitorCaMKP Inhibitor
CaMKP Inhibitor can inhibit CaMKP.
价 格：￥电议型 号：T2159产 地：中国大陆
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T21159Bis(2-ethylhexyl) sebacate；化合物 T21159Di(2-ethylhexyl) Sebacate|||Dioctyl Sebacate；Di(2-ethylhexyl) S
Bis(2-ethylhexyl) sebacate is used as a plasticizer in preparing ion-selective electrodes. It is an important raw material and intermediate used in organic synthesis, agrochemicals, pharmaceuticals and dyestuff fields.
价 格：￥电议型 号：T21159产 地：中国大陆
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T2103Ispinesib；伊斯平斯CK0238273|||SB-715992；伊匹尼塞|||伊斯平斯|||CK0238273|||SB-715992
Ispinesib (SB-715992), a selective, effectvie and reversible inhibitor of kinesin spindle protein (KSP), is derived from quinazolinone, with antineoplastic properties.
价 格：￥电议型 号：T2103产 地：中国大陆
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T20449AI3-15920；化合物 T20449AI3 15920；AI3 15920
AI3-15920 is an agent of biochemical.
价 格：￥电议型 号：T20449产 地：中国大陆
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T20448AI3-15932；化合物 T20448NSC 65607|||NSC65607|||NSC-65607；NSC 65607|||NSC65607|||NSC-65607
AI3-15932 is a part of a tetrahydroquinoline analog.
价 格：￥电议型 号：T20448产 地：中国大陆
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T2044Varespladib；伐瑞拉迪LY315920；LY315920|||伐瑞拉地|||伐瑞拉迪
Varespladib (LY315920), a specific and effective human non-pancreatic secretory phospholipase A2 (hnsPLA) inhibitor(IC50=7 nM), has been investigated for the treatment and prevention of sickle cell disease, vaso-occlusive crisis, and acute coronary syndrome.
价 格：￥电议型 号：T2044产 地：中国大陆
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T19771SXT1596；化合物 T19771NSC-65667|||SXT-1596|||NSC 65667|||SXT 1596|||NSC65667；NSC-65667|||SXT-1596|||NSC
SXT1596 is a novel SS18-SSX/TLE1 interaction inhibitor. SXT1596 reduces cell viability and reactivates EGR1 expression in synovial sarcoma.
价 格：￥电议型 号：T19771产 地：中国大陆
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T19658Enflurane；恩氟烷NSC115944|||Ethrane|||NSC-115944|||Efrane|||NSC 115944；NSC115944|||Ethrane|||NSC-115944
Enflurane (Efrane), a volatile anaesthetic, is a potent inhibitor of high conductance Ca2+-activated K+ channels of Chara australis. Enflurane is an internal standard in monitoring halogenated volatile anaesthetics by headspace gas chromatography-mass spectrometry. It allows rapid adjustments of anesthesia depth with little change in pulse or respiratory rate.
价 格：￥电议型 号：T19658产 地：中国大陆
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T19523PNU-159682 carboxylic acid；化合物 T19523PNU-159682 carboxylic acid
PNU-159682 carboxylic acid is a potent ADCs cytotoxin,PNU-159682 carboxylic acid has protein fold and diverse functions.
价 格：￥电议型 号：T19523产 地：中国大陆
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T19159Mal-β-CD化合物 Mal-β-CD6-O-alpha-D-Maltosyl-beta-cyclodextrin
Mal-β-CD is a cellular cholesterol modifier. It can form a soluble inclusion complex with cholesterol.
价 格：￥电议型 号：T19159产 地：中国大陆
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T18302Mal-Phe-C4-VC-PAB-DMEA-PNU-159682；化合物 T18302Mal Phe C4 VC PAB DMEA PNU 159682|||Mal-Phe-C4-VC-PAB-DM
Mal-Phe-C4-VC-PAB-DMEA-PNU-159682 is a drug-linker conjugate utilized in antibody-drug conjugate (ADC) therapy. It comprises the ADC linker Mal-Phe-C4-VC-PAB and the potent ADC cytotoxin DMEA-PNU-159682. DMEA-PNU-159682 encompasses metabolites of nemorubicin (MMDX) derived from liver microsomes, as well as the ADC cytotoxin PNU-159682[1].
价 格：￥电议型 号：T18302产 地：中国大陆
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T18292Mal-PEG4-VC-PAB-DMEA-PNU-159682；化合物 T18292Mal-PEG4-VC-PAB-DMEA-PNU159682|||MalPEG4VCPABDMEAPNU159682
Mal-PEG4-VC-PAB-DMEA-PNU-159682 is a drug-linker conjugate designed for antibody-drug conjugate (ADC) therapy. It combines the ADC linker, Mal-PEG4-VC-PAB, with the potent ADC cytotoxin, DMEA-PNU-159682. The cytotoxin, DMEA-PNU-159682, is derived from metabolites of nemorubicin (MMDX) found in liver microsomes, as well as the ADC cytotoxin PNU-159682[1].
价 格：￥电议型 号：T18292产 地：中国大陆
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T18246Mal-C2-Gly3-EDA-PNU-159682；化合物 T18246Mal-C2-Gly3-EDA-PNU-159682
Mal-C2-Gly3-EDA-PNU-159682, a drug-linker conjugate for antibody-drug conjugates (ADC), combines the cleavable ADC linker Mal-C2-Gly3-EDA with the potent ADC cytotoxin PNU-159682.
价 格：￥电议型 号：T18246产 地：中国大陆
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T18159m-PEG17-NHS ester；化合物 T18159m-PEG17-NHS ester
m-PEG17-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.
价 格：￥电议型 号：T18159产 地：中国大陆
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T17802DBCO-PEG4-VC-PAB-DMEA-PNU-159682；化合物 T17802DBCO-PEG4-VC-PAB-DMEA-PNU-159682|||DBCO PEG4 VC PAB DMEA
DBCO-PEG4-VC-PAB-DMEA-PNU-159682, a drug-linker conjugate for antibody-drug conjugates (ADC), comprises the ADC linker DBCO-PEG4-VC-PAB and the potent ADC cytotoxin DMEA-PNU-159682. The cytotoxin includes metabolites of nemorubicin (MMDX) from liver microsomes and the ADC cytotoxin PNU-159682[1].
价 格：￥电议型 号：T17802产 地：中国大陆
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T17292ZK159222；化合物 T17292ZK159222
ZK159222 is an effective 1α,25-(OH)2D3 receptor (VDR) agonist. ZK159222 has a partial agonistic character.
价 格：￥电议型 号：T17292产 地：中国大陆
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T17159Treosulfan；曲奥舒凡NSC 39069|||Treosulphan；NSC 39069|||曲奥舒凡|||Treosulphan
Treosulfan (Treosulphan) is a bifunctional alkylating agent. It also has activity in ovarian cancer and other solid tumor types.
价 格：￥电议型 号：T17159产 地：中国大陆
