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T15448GW-1100；化合物 T15448GW-1100
GW-1100 is a selective antagonist of GPR40 (pIC50: 6.9). GW1100 also plays the role of a GPR40 inverse agonist.
价 格：￥电议型 号：T15448产 地：中国大陆
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T15393Glycerol phenylbutyrate；苯丁酸甘油酯HPN-100；苯丁酸甘油酯|||HPN-100
Glycerol phenylbutyrate (HPN-100) (GPB) is a new generation ammonia scavenger drug and it also is a sigma-2 (σ2) receptor ligand (pKi: 8.02).
价 格：￥电议型 号：T15393产 地：中国大陆
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T15237Eperezolid；化合物EperezolidPNU-100592；PNU-100592
Eperezolid (PNU-100592) is an oxazolidinone antibacterial agent. Eperezolid showed well in vitro inhibitory activity, regardless of methicillin susceptibility for staphylococci(MIC90= 1-4 mg/ml).
价 格：￥电议型 号：T15237产 地：中国大陆
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T1520Aliskiren hemifumarate阿利克仑半富马酸盐阿利克仑半富马酸盐|||CGP 60536|||SPP 100|||CGP60536B
Aliskiren hemifumarate (CGP60536B) is an orally active nonpeptide renin inhibitor with antihypertensive activity.
价 格：￥电议型 号：T1520产 地：中国大陆
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T15198Edasalonexent；依达柰珍CAT-1004；CAT-1004
Edasalonexent (CAT-1004) is an orally available NF-κB inhibitor for the improvement of Duchenne muscular dystrophy.
价 格：￥电议型 号：T15198产 地：中国大陆
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T15166DPM-1001；化合物 T15166DPM-1001
DPM-1001 is an orally bioavailable and non-competitive protein-tyrosine phosphatase (PTP1B) inhibitor (IC50: 100 nM) with the anti-diabetic property.
价 格：￥电议型 号：T15166产 地：中国大陆
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T15100Desmethyl cariprazine；化合物 T15100Desmethyl cariprazine
Desmethyl cariprazine is a Cariprazine active metabolite. Cariprazine, an antipsychotic drug candidate, shows a high affinity for the D3 (Ki: 0.085 nM) and D2 (Ki: 0.49 nM) receptors, and moderate affinity for the 5-HT1A receptor (2.6 nM).
价 格：￥电议型 号：T15100产 地：中国大陆
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T14322ARP-100；化合物ARP-100MMP-2 Inhibitor III；MMP-2 Inhibitor III
ARP-100 (MMP-2 Inhibitor III) is a potent and selective matrix metalloproteinase MMP-2 inhibitor (IC50=12 nM). ARP-100 interacts with the S1´ pocket of MMP-2 and exhibits anti-invasive properties in an in vitro invasion Matrigel model. ARP-100 has low inhibitory activity against MMP-1 (>50 μM), MMP-3 (4.5 μM), MMP-7 (>50 μM) and MMP-9 (0.2 μM)[1][2].
价 格：￥电议型 号：T14322产 地：中国大陆
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T14100Acid-PEG2-SS-PEG2-acid；化合物 T14100Acid-PEG2-SS-PEG2-acid
Acid-PEG2-SS-PEG2-acid is a 4-unit PEG ADC linker that employs cleavable bonds. It is utilized in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T14100产 地：中国大陆
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T13560LAT-1002 TFA (835872-35-0 free base)；化合物 T13560LAT-1002 TFA；AT-1002 TFA
AT-1002 TFA is a tight junction regulator and absorption enhancer. It is a 6-mer synthetic peptide.
价 格：￥电议型 号：T13560L产 地：中国大陆
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T13560AT-1002；化合物 T13560AT-1002
AT-1002 is a tight junction regulator and absorption enhancer. It is a 6-mer synthetic peptide.
价 格：￥电议型 号：T13560产 地：中国大陆
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T13463LDihydrexidine；化合物 T13463LDAR-0100；DAR-0100
Dihydrexidine is a full efficacy D1-like dopamine receptor (D1/D5) agonist (IC50: 10 nM for D1 receptor). It also shows potent antiparkinsonian activity.
价 格：￥电议型 号：T13463L产 地：中国大陆
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T13463(+)-Dihydrexidine hydrochloride；化合物 T13463(+)-DAR-0100 (hydrochloride)；(+)-DAR-0100 (hydrochloride)
(+)-Dihydrexidine hydrochloride is an agonist of dopamine D1 receptor(EC50 of 72± 21 nM).
价 格：￥电议型 号：T13463产 地：中国大陆
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T13308Vortioxetine D8；化合物 T13308Lu AA 21004 D8；Lu AA 21004 D8
Vortioxetine D8 is a deuterium labeled Vortioxetine. Vortioxetine is an 5-HT1A, 5-HT1B, 5-HT3A, 5-HT7 receptor and SERT inhibitor (Kis: 15 nM, 33 nM, 3.7 nM, 19 nM and 1.6 nM, respectively).
价 格：￥电议型 号：T13308产 地：中国大陆
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T13295Veliflapon化合物 T13295DG-031|||BAY X 1005
Veliflapon is an orally active and selective inhibitor of 5-lipoxygenase activating protein (FLAP). Veliflapon inhibits the synthesis of the leukotrienes B4 and C4.
价 格：￥电议型 号：T13295产 地：中国大陆
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T13294Veledimex (S enantiomer)；化合物 T13294RG-115932 S enantiome|||INXN-1001 S enantiome；RG-115932 S enantio
Veledimex S enantiomer is the S enantiomer of veledimex. Veledimex is an oral activator ligand for a proprietary gene therapy promoter system and CYP3A4/5 inhibitor.
价 格：￥电议型 号：T13294产 地：中国大陆
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T13293LVeledimex；化合物 T13293LRG-115932|||INXN-1001；RG-115932|||INXN-1001
Veledimex is an oral activator ligand for a proprietary gene therapy promoter system. It is also a moderate inhibitor of and substrate for CYP3A4/5.
价 格：￥电议型 号：T13293L产 地：中国大陆
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T13293Veledimex racemate；化合物 T13293RG-115932 racemate|||INXN-1001 racemate；RG-115932 racemate|||INXN-1001
Veledimex racemate, the racemic form of veledimex, is an orally available, small-molecule ligand that activates the RheoSwitch Therapeutic System.
价 格：￥电议型 号：T13293产 地：中国大陆
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T131660Compound 0449-0100；化合物 0449-0100Compound 0449-0100
Compound 0449-0100 is a useful organic compound for research related to life sciences and the catalog number is T131660.
价 格：￥电议型 号：T131660产 地：中国大陆
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T13157LTG 100801 Hydrochloride；化合物 T13157LTG 100801 Hydrochloride
TG 100801 Hydrochloride is a prodrug to treat age-related macular degeneration. TG 100572 is a inhibitor of multi-targeted kinase(IC50s of 2, 7, 2, 16, 13, 5, 0.5, 6, 0.1, 0.4, 1, 0.2 for VEGFR1, VEGFR2, FGFR1, FGFR2, PDGFRβ, Fgr, Fyn, Hck, Lck, Lyn, Src, Yes, respectively).
价 格：￥电议型 号：T13157L产 地：中国大陆
