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T31390Desmetryn；化合物 T31390GS34360|||G-34360 G34360|||GS-34360|||GS 34360；GS34360|||G-34360 G34360|||GS-343
Desmetryn is a triazine herbicide.
价 格：￥电议型 号：T31390产 地：中国大陆
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T30624Buthiazide；化合物 T30624S-3500|||Saltucin|||Eunephran|||Butizidum|||S 3500；S-3500|||Saltucin|||Eunephra
Buthiazide, also known as Butizide, is a 3-isobutyl analog of hydrochlorothiazide.
价 格：￥电议型 号：T30624产 地：中国大陆
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T30602Bts 39542；化合物 T30602Bts-39542|||Bts39542；Bts-39542|||Bts39542
Bts 39542 is a diuretic that plays a major role in the Henle circulation and increases renal blood flow without affecting glomerular filtration rate.
价 格：￥电议型 号：T30602产 地：中国大陆
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T30520BMS-394136；化合物BMS-394136BMS394136|||BMS 394136|||BMS394136;UNII-M694U7167K；BMS394136|||BMS 394136|||
BMS-394136 (BMS 394136) is a KV1.5 antagonist for the treatment of cardiovascular diseases such as arrhythmias and atrial fibrillation.
价 格：￥电议型 号：T30520产 地：中国大陆
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T30519BMS-363131；化合物BMS-363131BMS363131|||BMS 363131；BMS363131|||BMS 363131
BMS-363131 (BMS363131) is a potent and selective trypsin inhibitor with an IC50 value of <1.7 nM.
价 格：￥电议型 号：T30519产 地：中国大陆
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T30518BMS-358233；化合物 T3051844U9QY574F|||BMS358233|||UNII-44U9QY574F；44U9QY574F|||BMS358233|||UNII-44U9QY57
BMS-358233 is an effective LCK inhibitor with excellent cell activity against T cell proliferation.
价 格：￥电议型 号：T30518产 地：中国大陆
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T30517BMS-354326；化合物 T30517BMS354326|||BMS 354326|||CHEMBL306448|||BDBM50144532；BMS354326|||BMS 354326|||C
BMS-354326 is a bio-active chemical.
价 格：￥电议型 号：T30517产 地：中国大陆
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T30516BMS-347070；化合物 T30516SCHEMBL6882900|||BMS 347070|||0CKM4H090C|||UNII-0CKM4H090C；SCHEMBL6882900|||BMS
BMS-347070 is a COX-2 inhibitor.
价 格：￥电议型 号：T30516产 地：中国大陆
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T30515BMS-346567；化合物 T30515BMS346567|||BMS 346567；BMS346567|||BMS 346567
BMS-346567 is a potent and selective dual angiotensin II and endothelin receptor antagonist.
价 格：￥电议型 号：T30515产 地：中国大陆
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T30514BMS-344577；化合物 T30514U259PQB19A|||UNII-U259PQB19A|||CHEMBL570867|||BMS 344577；U259PQB19A|||UNII-U259
BMS-344577, a lactam derivative based on arylguanidine, is a potent oral active FXA inhibitor with excellent susceptibility in vitro, good pharmacokinetics, and pharmacodynamics in animal models.
价 格：￥电议型 号：T30514产 地：中国大陆
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T30513BMS-317180；化合物 T30513BMS317180；BMS317180
BMS-317180 is a potent, novel, orally effective growth hormone secretagogue (GHS) that shows an excellent safety profile in preclinical studies. The compound was advanced into clinical development.
价 格：￥电议型 号：T30513产 地：中国大陆
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T29175YKAs3003；化合物 T29175YKAs-3003；YKAs-3003
YKAs3003, a potent inhibitor of pathogenic KAS III, displays minimal inhibitory concentration (MIC) values in the range 128-256 microg/mL against various bacteria.
价 格：￥电议型 号：T29175产 地：中国大陆
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T29140VU0652925；化合物 T29140VU 0652925|||BMS-3|||VU-0652925|||BMS3|||BMS 3；VU 0652925|||BMS-3|||VU-0652925||
VU0652925 is a PAR4 antagonist. VU0652925 has a P-sel IC50 of 39.2 pM (-pIC50±SEM: 10.41±0.04) and a PAC1 IC50 of 43.0 pM (-pIC50±SEM: 10.4±0.04).
价 格：￥电议型 号：T29140产 地：中国大陆
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T28648S39625；化合物 T28648S-39625|||S 39625；S-39625|||S 39625
S39625, an E-ring camptothecin keto analogue, is a stable, potent, and selective topoisomerase I inhibitor without being substrates of drug efflux transporters. Nanomolar concentrations of S39625 induces intense and persistent histone gamma-H2AX. The chemical stability of the keto analogues and the ability of S39625 to produce high levels of persistent Top1-DNA cleavage complex and its potent antiproliferative activity against human cancer cell lines make S39625 a promising new anticancer drug c
价 格：￥电议型 号：T28648产 地：中国大陆
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T28647S33084；化合物 T28647S 33084|||S-33084；S 33084|||S-33084
S33084 is a potent, selective and competitive antagonist of dopamine D(3)-receptors.
价 格：￥电议型 号：T28647产 地：中国大陆
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T28646S-312-d；化合物 T28646S312-d|||S 312-d|||S-312d|||S 312d；S312-d|||S 312-d|||S-312d|||S 312d
S-312d is a calcium channel antagonist. S-312-d can offer marked neuronal protective effects against ischemic injury.
价 格：￥电议型 号：T28646产 地：中国大陆
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T2830Betulinic acid；白桦脂酸ALS-357|||Lupatic acid|||Betulic acid；白桦脂酸|||桦木酸|||ALS-357|||Lupatic acid|||Betul
Betulinic acid (ALS-357) is a pentacyclic lupane-type triterpene derivative of betulin (isolated from the bark of Betula alba, the common white birch) which has antiretroviral, antimalarial, and anti-inflammatory properties, as well as a more recently discovered potential as an anticancer agent, by inhibition of topoisomerase.
价 格：￥电议型 号：T2830产 地：中国大陆
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T28253Ono-RS 347；化合物 T28253Ono-RS-347|||Ono RS 347|||Ono RS-347；Ono-RS-347|||Ono RS 347|||Ono RS-347
Ono-RS 347 is a leukotriene antagonists with the activity of SRS-A antagonist.
价 格：￥电议型 号：T28253产 地：中国大陆
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T28105MRS3558；化合物 T28105MRS-3558|||MRS 3558；MRS-3558|||MRS 3558
MRS3558 is an agonist of A3 adenosine receptors.
价 格：￥电议型 号：T28105产 地：中国大陆
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T28038Milademetan HCl (1398568-47-2 free base)；化合物 T28038Milademetan HCl|||DS3032|||DS 3032|||DS-3032|||DS
Milademetan is a potent and selective MDM2 inhibitor. MDM2 inhibitor DS-3032b binds to and prevents the binding of MDM2 protein to the transcriptional activation domain of the tumor suppressor protein p53 upon oral administration. By preventing this MDM2-p53 interaction, the proteosome-mediated enzymatic degradation of p53 is inhibited and the transcriptional activity of p53 is restored. This results in the restoration of p53 signaling and leads to the p53-mediated induction of tumor cell apopto
价 格：￥电议型 号：T28038产 地：中国大陆
