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T12052Mivobulin；化合物 T12052(S)-(-)-NSC 613862|||NSC 613862；(S)-(-)-NSC 613862|||NSC 613862
Mivobulin is an inhibitor of tubulin .
价 格：￥电议型 号：T12052产 地：中国大陆
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T11979McN5691；化合物 McN5691MCN 5691|||RWJ26240；MCN 5691|||RWJ26240
McN5691 (RWJ26240) is a voltage-dependent calcium channel blocker with antihypertensive activity that can be used in the study of diseases caused by vascular smooth muscle abnormalities.
价 格：￥电议型 号：T11979产 地：中国大陆
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T11962MC3482；化合物MC3482MC3482
MC3482 is a specific inhibitor of sirtuin5 (SIRT5).
价 格：￥电议型 号：T11962产 地：中国大陆
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T11893LLurasidone metabolite 14326 hydrochloride；化合物 T11893LLurasidone metabolite 14326 hydrochloride (1862
Lurasidone metabolite 14326 hydrochloride, an active metabolite of the atypical antipsychotic Lurasidone, maintains its significant function in pharmacological efficacy.
价 格：￥电议型 号：T11893L产 地：中国大陆
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T11862LMD-009；化合物 T11862LMD-009
LMD-009 mediates chemotaxis, inositol phosphate accumulation, and calcium release in high potencies with EC50s from 11 to 87 nM. LMD-009 is a selective CCR8 nonpeptide agonist.
价 格：￥电议型 号：T11862产 地：中国大陆
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T11809L162441；化合物 T11809L162441
L162441 is an antagonist of Angiotensin type 1 receptor.
价 格：￥电议型 号：T11809产 地：中国大陆
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T11808L162389；化合物 T11808L162389
L162389 is a potent angiotensin AT1 receptor antagonist with Ki of 28 nM.
价 格：￥电议型 号：T11808产 地：中国大陆
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T1178Temozolomide；替莫唑胺NSC 362856|||TZM|||CCRG 81045|||TMZ；NSC 362856|||替莫唑胺|||TZM|||CCRG 81045|||TMZ
Temozolomide (TMZ) is a DNA alkylating agent with blood-brain barrier permeability and oral activity. Temozolomide has antitumor activity and antiangiogenic activity, and also induces apoptosis and autophagy. Temozolomide is stable under acidic conditions and hydrolyzes under neutral or slightly alkaline conditions.
价 格：￥电议型 号：T1178产 地：中国大陆
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T11762LKira8；化合物Kira8AMG-18；AMG-18
Kira8 (AMG-18) is a mono-selective IRE1α inhibitor that allosterically attenuates IRE1α RNase activity (IC50: 5.9 nM).
价 格：￥电议型 号：T11762L产 地：中国大陆
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T11762Kira8 Hydrochloride；化合物 T11762AMG-18 Hydrochloride；AMG-18 Hydrochloride
Kira8 Hydrochloride is a mono-selective IRE1α inhibitor that allosterically attenuates IRE1α RNase activity with an IC50 of 5.9 nM.
价 格：￥电议型 号：T11762产 地：中国大陆
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T11675Irbesartan-d4；厄贝沙坦 D4SR-47436 D4|||BMS-186295 D4；厄贝沙坦 D4|||SR-47436 D4|||BMS-186295 D4
Irbesartan D4, a deuterium-labeled variant of Irbesartan, is a highly potent and specific antagonist of the angiotensin II type 1 (AT1) receptor.
价 格：￥电议型 号：T11675产 地：中国大陆
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T11662LINT-777；化合物INT-777S-EMCA；S-EMCA
INT-777 (S-EMCA) is a potent TGR5 agonist with an EC50 of 0.82 μM. INT-777 (S-EMCA) inhibits NLRP5-ASC inflammasome-mediated neuroinflammation via the TGR3/cAMP/PKA signaling pathway after subarachnoid hemorrhage in rats.
价 格：￥电议型 号：T11662L产 地：中国大陆
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T11662INT-777 R-enantiomer；化合物 T11662S-EMCA R enantiomer；S-EMCA R enantiomer
INT-777 is the R-enantiomer of INT-777, less potent than INT-777,EC50 of 4.79 μM for TGR5.
价 格：￥电议型 号：T11662产 地：中国大陆
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T11629Ifenprodil glucuronide；化合物 T11629Ifenprodil glucuronide
Ifenprodil glucuronide, a derivative of Ifenprodil, is a vasodilator and an inhibitor of platelet aggregation. In contrast to Ifenprodil, Ifenprodil glucuronide does not affect platelet aggregation nor arterial contraction.
价 格：￥电议型 号：T11629产 地：中国大陆
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T11628IACS-8968 S-enantiomer；化合物 T11628IDO/TDO Inhibitor (S-enantiomer)；IDO/TDO Inhibitor (S-enantiomer)
IACS-8968 S-enantiomer is the S-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
价 格：￥电议型 号：T11628产 地：中国大陆
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T11627IACS-8968 R-enantiomer；化合物 T11627IDO/TDO Inhibitor (R-enantiomer)；IDO/TDO Inhibitor (R-enantiomer)
IACS-8968 R-enantiomer is the R-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
价 格：￥电议型 号：T11627产 地：中国大陆
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T11626IACS-8968；化合物 T11626IDO/TDO Inhibitor；IDO/TDO Inhibitor
IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
价 格：￥电议型 号：T11626产 地：中国大陆
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T11625IDO1 and HDAC1 Inhibitor；化合物 T11625IDO1 and HDAC1 Inhibitor
IDO1 and HDAC1 Inhibitor is a dual IDO1 and HDAC1 inhibitor (IC50s: 69.0 nM and 66.5 nM).
价 格：￥电议型 号：T11625产 地：中国大陆
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T11624IDO1-IN-2；化合物 T11624IDO1-IN-2
IDO1-IN-2 is a potent and selective IDO1 inhibitor with IC50s of 81 nM, 59 nM (mouse), and 28 nM (rat), respectively. It has anti-cancer activity.
价 格：￥电议型 号：T11624产 地：中国大陆
