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T12832AmcenestrantSAR439859
SAR439859 is an orally active, nonsteroidal and selective degrader of estrogen receptor (SERD). SAR439859 is a potent antagonist of ER (with an EC50 of 0.2 nM for ERα degradation).
价 格：￥电议型 号：T12832产 地：中国大陆
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T12831LSAR405
SAR-405 is a potent and selective PIK3C3/Vps34 inhibitor (IC50:1.2 nM; Kd:1.5 nM) that prevents autophagy and synergizes with MTOR inhibition in tumor cells. SAR405 treatment also inhibits autophagy induced either by starvation or by MTOR (mechanistic tar
价 格：￥电议型 号：T12831L产 地：中国大陆
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T12831SAR405 R enantiomer
SAR405 R enantiomer is the less active enantiomer of SAR405. SAR405 is an inhibitor of PIK3C3/Vps34.
价 格：￥电议型 号：T12831产 地：中国大陆
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T1107Sarafloxacin hydrochloride盐酸沙拉沙星；A-56620 HCl；Sarafloxacin HCl；A-56620 (hydrochloride)
Sarafloxacin hydrochloride, a quinolone antibiotic drug, is a hydrochloride salt form of sarafloxacin.
价 格：￥电议型 号：T1107产 地：中国大陆
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T1057AzilsartanTAK-536；阿齐沙坦
Azilsartan is an Angiotensin 2 Receptor Blocker. The mechanism of action of azilsartan is as an Angiotensin 2 Type 1 Receptor Antagonist. The physiologic effect of azilsartan is by means of Decreased Blood Pressure.
价 格：￥电议型 号：T1057产 地：中国大陆
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T0215LLosartan氯沙坦；洛沙坦；DuP-753
Losartan is an angiotensin II receptor antagonist.
价 格：￥电议型 号：T0215L产 地：中国大陆
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T0215Losartan potassiumDuP-753 potassium；MK 954；DuP 753；洛沙坦钾；氯沙坦钾
Losartan, an Angiotensin II Receptor Blocker, selectively and competitively blocks the binding of angiotensin II to the angiotensin I (AT1) receptor.
价 格：￥电议型 号：T0215产 地：中国大陆
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T0215Losartan potassiumLosartan potassium,DuP-753 potassium,MK 954
Losartan, an Angiotensin II Receptor Blocker, selectively and competitively blocks the binding of angiotensin II to the angiotensin I (AT1) receptor.
价 格：￥电议型 号：T0215产 地：美洲
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T0215LLosartanLosartan,DuP-753,
Losartan is an angiotensin II receptor antagonist.
价 格：￥电议型 号：T0215L产 地：美洲
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T10440Azilsartan D5Azilsartan D5,TAK-536 D5,
Azilsartan (TAK-536) D5 is the deuterium-labeled Azilsartan. Azilsartan is a specific antagonist of the angiotensin II type 1 receptor.
价 格：￥电议型 号：T10440产 地：美洲
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T1057AzilsartanAzilsartan,TAK-536,
Azilsartan is an Angiotensin 2 Receptor Blocker. The mechanism of action of azilsartan is as an Angiotensin 2 Type 1 Receptor Antagonist. The physiologic effect of azilsartan is by means of Decreased Blood Pressure.
价 格：￥电议型 号：T1057产 地：美洲
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T10670Candesartan D4Candesartan D4,CV-11974 D4,
Candesartan D4 is the deuterium labeled Candesartan. Candesartan is an antagonist of angiotensin II receptor.
价 格：￥电议型 号：T10670产 地：美洲
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T1107Sarafloxacin hydrochlorideSarafloxacin hydrochloride,A-56620 (hydrochloride),Sarafloxacin HCl
Sarafloxacin hydrochloride, a quinolone antibiotic drug, is a hydrochloride salt form of sarafloxacin.
价 格：￥电议型 号：T1107产 地：美洲
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T11599Ibiglustat L-Malic acidIbiglustat L-Malic acid,Venglustat (L-Malic acid),SAR402671 (L-Malic acid)
Ibiglustat L-Malic acid (Venglustat L-Malic acid), a potential therapy for PD Parkinson’s disease.
价 格：￥电议型 号：T11599产 地：美洲
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T12831SAR405 R enantiomerSAR405 R enantiomer
SAR405 R enantiomer is the less active enantiomer of SAR405. SAR405 is an inhibitor of PIK3C3/Vps34.
价 格：￥电议型 号：T12831产 地：美洲
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T12831LSAR405SAR405
SAR405 suppresses autophagy induced either by starvation or by mTOR inhibition. SAR405 is a first-in-class and ATP-competitive inhibitor of PI3K class III isoform Vps34 (IC50=1.2 nM; Kd=1.5 nM).
价 格：￥电议型 号：T12831L产 地：美洲
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T12834Saroglitazar MagnesiumSaroglitazar Magnesium
Saroglitazar Magnesium is a novel agonist of peroxisome proliferator-activated receptor (PPAR)(predominant PPARα and moderate PPARγ activity with EC50 values of 0.65 pM and 3 nM in HepG2 cells, respectively).
价 格：￥电议型 号：T12834产 地：美洲
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T12835SaroglitazarSaroglitazar
Saroglitazar is a novel agonist of peroxisome proliferator-activated receptor (PPAR)(predominant PPARα and moderate PPARγ activity with EC50 values of 0.65 pM and 3 nM in HepG2 cells, respectively).
价 格：￥电议型 号：T12835产 地：美洲
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T12849SAR7334SAR7334
SAR7334 is a potent and specific inhibitor of TRPC6(IC50 of 7.9 nM).
价 格：￥电议型 号：T12849产 地：美洲
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T12849LSAR7334 hydrochlorideSAR7334 hydrochloride
SAR7334 hydrochloride is a potent and specific inhibitor of TRPC6(IC50 of 7.9 nM).
价 格：￥电议型 号：T12849L产 地：美洲
