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T73094Adhesamine；化合物 AdhesamineAdhesamine
Adhesamine, a dumbbell-shaped molecule, plays a crucial role in activating the MAPK/FAK pathway, thus promoting mammalian cell adhesion and growth. Additionally, it accelerates the differentiation and enhances the survival of mice hippocampal neurons in primary culture.
价 格：￥电议型 号：T73094产 地：中国大陆
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T7295015-PGDH-IN-1；化合物 15-PGDH-IN-115-PGDH-IN-1
15-PGDH-IN-1 is an orally active, potent inhibitor of 15-PGDH, exhibiting significant inhibitory activity against recombinant human 15-PGDH with an IC50 value of 3 nM. This compound is utilized in the research of tissue repair and regeneration.
价 格：￥电议型 号：T72950产 地：中国大陆
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T72948hDHODH-IN-11；化合物 hDHODH-IN-11hDHODH-IN-11
hDHODH-IN-11, a potent inhibitor of human dihydroorotate dehydrogenase (hDHODH), exhibits an IC50 value of 7.2 nM and has low cytotoxicity. It is applicable in acute myeloid leukemia (AML) research.
价 格：￥电议型 号：T72948产 地：中国大陆
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T72705IDH1 Inhibitor 7；化合物 IDH1 Inhibitor 7IDH1 Inhibitor 7
IDH1 Inhibitor 7 is an IDH1 inhibitor with an IC 50 of less than 100 nM [1] .
价 格：￥电议型 号：T72705产 地：中国大陆
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T72283(+)-Dihydrocalanolide A；化合物 (+)-Dihydrocalanolide ANSC 678323|||DHCal A ; NSC 678323|||DHCal A；NSC
(+)-Dihydrocalanolide A (DHCal A; NSC 678323), an orally active nonnucleoside inhibitor of reverse transcriptase, is utilized in research related to HIV infection.
价 格：￥电议型 号：T72283产 地：中国大陆
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T70684DHPM-93；化合物 DHPM-93DHPM-93
DHPM-93 is a the most potent inhibitor of sodium iodide symporter (nis) reported to date
价 格：￥电议型 号：T70684产 地：中国大陆
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T70006DHA-paclitaxel；化合物 DHA-paclitaxelDHA-paclitaxel
DHA-paclitaxel, also know as Taxoprexin, is prodrug comprised of the naturally occurring omega-3 fatty acid docosahexaenoic acid (DHA) covalently conjugated to the anti-microtubule agent paclitaxel. Because tumor cells take up DHA, DHA-paclitaxel is delivered directly to tumor tissue, where the paclitaxel moiety binds to tubulin and inhibits the disassembly of microtubules, thereby resulting in the inhibition of cell division. Paclitaxel also induces apoptosis by binding to and blocking the func
价 格：￥电议型 号：T70006产 地：中国大陆
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T69409DH-97；化合物 DH-97DH-97
DH-97 is a potent MT2 melatonin receptor antagonist (pKi value = 8.03).
价 格：￥电议型 号：T69409产 地：中国大陆
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T69199Homopteroic Acid；化合物 Homopteroic AcidHomopteroic Acid
Homopteroic Acid is an intermediate in the synthesis of Homofolic Acid which inhibits the growth of L1210 mouse leukemia cells when intracellular folates are acquired via the high-affinity folate binding protein.
价 格：￥电议型 号：T69199产 地：中国大陆
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T67928NDH-1 inhibitor-1；NDH-1抑制剂-1NDH-1 inhibitor-1
NDH-1 inhibitor-1 is an effective NDH-1 inhibitor, which can inhibit bovine SMP (mitochondrial granules), potato SMP and Escherichia coli, with pI50 values of <4, 5.40, 6.15 ?M, respectively.
价 格：￥电议型 号：T67928产 地：中国大陆
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T67875DHODH-IN-23；化合物DHODH-IN-23DHODH-IN-23
DHODH-IN-23 is a DHODH inhibitor with oral activity. DHODH-IN-23 is often used in cancer research.
价 格：￥电议型 号：T67875产 地：中国大陆
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T67832ALDH2 modulator 1；ALDH2调节剂1ALDH2 modulator 1
ALDH2 modulator 1 is a potent and orally active modulator of acetaldehyde dehydrogenase-2 (ALDH2), which reduces blood alcohol levels in mice.
价 格：￥电议型 号：T67832产 地：中国大陆
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T65235Hexahydrohippuric acid；化合物 Hexahydrohippuric acidHexahydrohippuric acid
Hexahydrohippuric acid is a useful organic compound for research related to life sciences. The catalog number is T65235 and the CAS number is 32377-88-1.
价 格：￥电议型 号：T65235产 地：中国大陆
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T64662MDH1/2 inhibitor compound 16c；化合物 MDH1/2 inhibitor compound 16cMDH1/2 inhibitor compound 16c
MDH1/2 inhibitor compound 16c is a useful organic compound for research related to life sciences and the catalog number is T64662.
价 格：￥电议型 号：T64662产 地：中国大陆
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T64371Virodhamine；化合物VirodhamineO-arachidonoyl ethanolamine；O-arachidonoyl ethanolamine
Virodhamine (O-arachidonoyl ethanolamine), an endocannabinoid, is an antagonist of CB1 receptor and an agonist of CB2 receptor. Virodhamine can be used for the research of neurological disorders such as Alzheimer´s diseases.
价 格：￥电议型 号：T64371产 地：中国大陆
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T64367Fmoc-Dha-OH；化合物Fmoc-Dha-OH2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)prop-2-enoic acid；2-({[(9H-fl
Fmoc-Dha-OH (2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)prop-2-enoic acid) is a biologically active compound that is an important component of peptide and protein synthesis. It is commonly used in the synthesis of peptide-based drugs, as well as in the study of protein-protein interactions, protein folding and protein engineering.
价 格：￥电议型 号：T64367产 地：中国大陆
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T64347ALDH1A3-IN-3；化合物ALDH1A3-IN-3ALDH1A3-IN-3
ALDH1A3-IN-3 (compound 16), a powerful ALDH1A3 inhibitor with an IC50 of 0.26 μM, serves as an effective ALDH3A1 substrate. It is utilized in prostate cancer research.
价 格：￥电议型 号：T64347产 地：中国大陆
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T64228ALDH1A1-IN-3；化合物 ALDH1A1-IN-3ALDH1A1-IN-3
ALDH1A1-IN-3 is a good and selective inhibitor of aldehyde dehydrogenase 1A1 (ALDH1A1) (IC50: μM).ALDH1A1-IN-3 is effective in improving glucose consumption in HepG2 cells.ALDH1A1-IN-3 can be used for studies to improve glucose metabolism.
价 格：￥电议型 号：T64228产 地：中国大陆
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T64146RORγt/DHODH-IN-3；化合物 RORγt/DHODH-IN-3RORγt/DHODH-IN-3
RORγt/DHODH-IN-3 (compound (S)-14d) is a potent, orally active dual inhibitor of RORγt (IC50: 0.098 μM) and DHODH (IC50: 0.432 μM).RORγt/DHODH-IN-1 has significant in vivo anti-inflammatory effects.
价 格：￥电议型 号：T64146产 地：中国大陆
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T64145RORγt/DHODH-IN-1；化合物 RORγt/DHODH-IN-1RORγt/DHODH-IN-1
RORγt/DHODH-IN-1 (compound (R)-14d) is a potent, orally active dual inhibitor of RORγt (IC50: 0.083 μM) and DHODH (IC50: 0.172 μM), which exhibits significant in vivo anti-inflammatory effects.
价 格：￥电议型 号：T64145产 地：中国大陆
