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T38720SR-31747 free base；SR-31747 free baseSR-31747 free base
SR-31747 free base is an immunosuppressive and anti-inflammatory sigma ligand that efficiently inhibits cell proliferation through the inhibition of sterol isomerase activity.
价 格：￥电议型 号：T38720产 地：中国大陆
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T38683SCD1 inhibitor-3；化合物SCD1 inhibitor-3SCD1-IN-3|||SCD1 inhibitor-3|||SCD1 inhibitor 17a；SCD1-IN-3|||SC
SCD1 inhibitor-3 (ML-270) is a highly effective and orally available compound that inhibits SCD1 with remarkable safety. SCD1 inhibitor-3 demonstrates strong potential for research in metabolic diseases, including obesity, type II diabetes, and dyslipidemia, as well as various skin conditions like acne and cancer.
价 格：￥电议型 号：T38683产 地：中国大陆
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T36982CXCR3 Antagonist 6cCXCR3 Antagonist 6cCXCR-3 Antagonist 6c|||CXCR3 Antagonist 6c
CXCR3 antagonist 6c is an antagonist of chemokine (C-X-C motif) receptor 3 (CXCR3).1It inhibits calcium mobilization induced by chemokine (C-X-C motif) ligand 11 (CXCL11) in HEK293 cells expressing the human receptor (IC50= 0.06 μM). It is selective for CXCR3 over a panel of 14 human G protein-coupled receptors at 10 μM. CXCR3 antagonist 6c inhibits CXCR3-mediated migration of isolated human T cells (IC50= ~100 nM).
价 格：￥电议型 号：T36982产 地：中国大陆
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T36569KR-32568；化合物KR-32568KR-32568
KR-32568 is a sodium/hydrogen exchanger 1 (NHE-1) inhibitor (IC50: 230 nM). KR-32568 exhibits potent cardioprotective effects. When used at a concentration of 10 μM, it restored cardiac systolic function in an isolated ischemic rat heart model. KR-32568 (0.3 mg/kg) reduced the size of myocardial infarction in a rat model of ischemia and reperfusion injury.
价 格：￥电议型 号：T36569产 地：中国大陆
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T36289Protease-Activated Receptor-3 (PAR-3) (1-6), human TFA；Protease-Activated Receptor-3 (PAR-3) (1-6),
Protease-Activated Receptor-3 (PAR-3) (1-6), human TFA is a peptide that acts as an agonist for the proteinase-activated receptor (PAR-3)[1].
价 格：￥电议型 号：T36289产 地：中国大陆
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T36286Protease-Activated Receptor-3 (PAR-3) (1-6), human；PAR-3 (1-6) amide (human)Protease-Activated Recep
TFRGAP-amide, human PAR-3-derived tethered ligand sequence which does not activate PAR-3 but rather activates PAR-1 and PAR-2, either in Jurkat or in other PAR-expressing cells.
价 格：￥电议型 号：T36286产 地：中国大陆
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T35186XR 334；化合物 T35186XR-334|||XR334；XR-334|||XR334
XR 334 is a biochemical.
价 格：￥电议型 号：T35186产 地：中国大陆
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T35074VRT-325；化合物VRT-325CFcor 325|||VRT-534|||CFcor325|||VRT 325|||VRT325|||CF-106951|||CFcor-325；CFcor 32
VRT-325 can repair folding defects by promoting dimerization of the two NBDs or by promoting folding of the TMD.VRT-325 accelerates the healing rate of CF cell monolayers.
价 格：￥电议型 号：T35074产 地：中国大陆
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T35038Vapiprost hydrochloride；化合物 T35038GR32191B|||GR 32191B|||GR-32191B；GR32191B|||GR 32191B|||GR-32191B
Vapiprost hydrochloride is a biochemicla.
价 格：￥电议型 号：T35038产 地：中国大陆
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T34616Seridopidine；化合物SeridopidineACR-343|||ACR 343|||ACR343；ACR-343|||ACR 343|||ACR343
Seridopidine (ACR343) is a modulator of dopaminergic activity that is used as an oral therapy for schizophrenia, Parkinson´s disease, and Tourette´s syndrome.
价 格：￥电议型 号：T34616产 地：中国大陆
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T34401Roxoperone；化合物 T34401R 7158|||F-33|||FR-33|||NSC 186062|||Roxoperon；R 7158|||F-33|||FR-33|||NSC 1860
Roxoperone is a bioactive chemical.
价 格：￥电议型 号：T34401产 地：中国大陆
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T33816Ordopidine；奥多匹定ACR-325|||ACR 325|||ACR325；ACR-325|||ACR 325|||ACR325
Ordopidine (ACR325) is a dopaminergic stabilizer that suppresses psychostimulant-induced hyperactivity disorder and stimulates behavior during inactivity. Ordopidine acts as a dopamine D2 receptor antagonist in vitro and, despite its low affinity, its specific state-dependent behavioral effect characteristics are not generally shared by D2 receptor antagonists.
价 格：￥电议型 号：T33816产 地：中国大陆
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T32058Henagliflozin；化合物 T32058SHR3824|||SHR 3824|||SHR-3824；SHR3824|||SHR 3824|||SHR-3824
Henagliflozin (SHR3824) is an effective, oral, and selective SGLT2 inhibitor that effectively inhibits human SGLT2 in vitro, but has very weak inhibitory effects on human SGLT1.
价 格：￥电议型 号：T32058产 地：中国大陆
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T31796FK409；化合物 T31796NOR-3|||NOR 3|||FK 409|||FK-409|||NOR3；NOR-3|||NOR 3|||FK 409|||FK-409|||NOR3
FK409 is a cell permeable NO donor which produces vasorelaxation.
价 格：￥电议型 号：T31796产 地：中国大陆
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T31741Facinicline (free base)；化合物 T31741MEM-3454|||RO-5313534|||RG-3487|||RG3487|||R-3487|||Facinicline；ME
Facinicline (free base) is a partial agonist of the nicotinic alpha-7 (α7) receptor. It is used for the oral treatment of Alzheimer´s.
价 格：￥电议型 号：T31741产 地：中国大陆
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T31566Doranidazole；化合物 T31566PR-350|||PR350|||PR-000350|||RP-343|||PR000350；PR-350|||PR350|||PR-000350|||R
Dornidazole (PR-000350, PR-350, RP-343, PR-69) is an effective radiosensitizer for hypoxic cells with the potential for the treatment of non-small cell lung cancer (NSCLC) and pancreatic cancer.
价 格：￥电议型 号：T31566产 地：中国大陆
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T31089CR 39；化合物 T31089PADC|||CR39|||PM 600|||CR-39|||Lantrak 2；PADC|||CR39|||PM 600|||CR-39|||Lantrak 2
CR 39, a plastic, can be used as a charged particle detector for superimposed autoradiography tissue images.
价 格：￥电议型 号：T31089产 地：中国大陆
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T30580BRD4-Kinases-IN-3；化合物 T30580BRD4 kinases inhibitor 3|||BRD4-Kinases inhibitor-3；BRD4 kinases inhibit
BRD4-Kinases-IN-3 is a dual BRD4-Kinases inhibitor that can be used as a value-added multi-targeted chemical probe for cancer therapy.
价 格：￥电议型 号：T30580产 地：中国大陆
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T29746AHR 376；化合物 T29746AHR376|||AHR-376；AHR376|||AHR-376
AHR 376 is a biochemical.
价 格：￥电议型 号：T29746产 地：中国大陆
