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产品数:86101
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已选条件
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TQ0156GW1929GW 1929,GW1929,Peroxisome proliferator-activated receptors,PPAR,inhibit,GW-1929,Inhibitor
GW1929 is a potent PPAR-γ agonist (pKi: 8.84 for human PPAR-γ; pEC50s of 8.56 and 8.27 for human and murine PPAR-γ).
价 格:¥电议型 号:TQ0156产 地:中国大陆
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T12565PRX933 hydrochloride
PRX933 hydrochloride is an agonist of 5-HT2C receptor and can be used in studies about hypertension acute treatment.
价 格:¥电议型 号:T12565产 地:中国大陆
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T7567LAdrenorphin 3TFA(88377-68-8(free base))Adrenorphin 3TFA(88377688(free base)),Adrenorphin 3TFA(88377
Adrenorphin(3TFA) is an agonist of μ-opioid receptor(Ki :12 nM).
价 格:¥电议型 号:T7567L产 地:中国大陆
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T6651Safinamide mesylateEMD 1195686,Monoamine Oxidase,EMD-1195686,neuroprotective,inhibit,OGD/R,Glucose,n
Safinamide Mesylate, a mesylate salt of Safinamide, can reversibly and specifically inhibit MAO-B (IC50: 98 nM), has 5918-fold selectivity against MAO-A.
价 格:¥电议型 号:T6651产 地:中国大陆
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T8560Angiotensin II human acetateAngiotensin Receptor,Inhibitor,Angiotensin II human,inhibit,Angiotensin
Angiotensin II acetate is a vasoconstrictor that mainly acts on the AT1 receptor.
价 格:¥电议型 号:T8560产 地:中国大陆
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T21302LUNC 569 hydrochlorideUNC 569 hydrochloride
UNC 569 hydrochloride is a reversible and ATP-competitive inhibitor of Mer with an IC50 of 2.9 nM and a Ki of 4.3 nM. UNC 569 hydrochloride inhibits Axl and Tyro3 with IC50s of 37 nM and 48 nM, respectively. UNC 569 hydrochloride can be used in studies about acute lymphoblastic leukemia and atypical teratoid/rhabdoid tumors.
价 格:¥电议型 号:T21302L产 地:中国大陆
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TN5634Aureusidinanti-inflammatory effects,LOX,Lipoxygenase,antioxidant,inhibit,Aureusidin,Reactive Oxygen
Aureusidin shows antioxidant and lipoxygenase inhibitory activity with anti-inflammatory effects.
价 格:¥电议型 号:TN5634产 地:中国大陆
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T8856Ascorbyl Propyl HyaluronateAscorbyl Propyl Hyaluronate
Ascorbyl propyl hyaluronate is a perfect combination of hyaluronic acid and vitamin C, to overcome the instability of vitamin C, is to improve wrinkles, moisturize, calm the skin, whitening quality raw materials.
价 格:¥电议型 号:T8856产 地:中国大陆
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TP1156H-Gly-Gly-Pro-OHInhibitor,HGlyGlyProOH,inhibit,H Gly Gly Pro OH
H-Gly-Pro-OH is a dipeptide composed of glycine and proline, and is an end product of collagen metabolism that is further cleaved by prolidase.
价 格:¥电议型 号:TP1156产 地:中国大陆
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T75653-Hydroxycapric acidEndogenous Metabolite,3Hydroxycapric acid,Inhibitor,3 Hydroxycapric acid,3-Hydro
3-hydroxydecanoic acid is a medium-chain fatty acid. It has a role as an antimitotic and an Escherichia coli metabolite.
价 格:¥电议型 号:T7565产 地:中国大陆
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TP1101Nonapeptide-1 acetate salt (158563-45-2 free base)Nonapeptide1 acetate salt (158563452 free base),No
Nonapeptide-1 acetate salt, a peptide hormone, is a potent α-Melanocyte-stimulating hormone (α-MSH) antagonist, with an IC50 of 11 nM. Nonapeptide-1 acetate salt Nonapeptide-1 acetate salt, a peptide hormone, is a potent α-Melanocyte-stimulating hormone (α-MSH) antagonist, with an IC50 of 11 nM.
价 格:¥电议型 号:TP1101产 地:中国大陆
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T67756ISRIB-A15
ISRIB-A15 is an potent inhibitor of the integrated stress response with an EC50 of 0.8 nM.
价 格:¥电议型 号:T67756产 地:中国大陆
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TN7156(S)-(+)-ochracin
(S)-(+)-ochracin is a marine derived natural products found in Helicascus kanaloanus.
价 格:¥电议型 号:TN7156产 地:中国大陆
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T6563LDC000067LDC000067,CDK,LDC-067,Apoptosis,Cyclin dependent kinase,LDC 000067,LDC-000067,inhibit,LDC 0
LDC000067 is a highly specific and selective CDK9 inhibitor with an IC50 value of 44±10 nM.
价 格:¥电议型 号:T6563产 地:中国大陆
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T9856FLT3-IN-10
FLT3-IN-10 (compound 7c) is a potent inhibitor of FMS-like tyrosine kinase 3 (FLT3). FLT3-IN-10 shows the potential for the treatment of FLT3-mutated acute myeloid leukemia (AML).
价 格:¥电议型 号:T9856产 地:中国大陆
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TN1560Dehydroeffusolinhibit,Inhibitor,Dehydroeffusol,Apoptosis
Dehydroeffusol possesses anti-cancer, anxiolytic and sedative properties. Dehydroeffusol inhibits gastric cancer cell growth and tumorigenicity by selectively inducing tumor-suppressive endoplasmic reticulum stress and a moderate apoptosis.
价 格:¥电议型 号:TN1560产 地:中国大陆
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T6256YYA-021YYA 021;YYA021
YYA-021 inhibits HIV entry, with high anti-HIV activity and low cytotoxicity.
价 格:¥电议型 号:T6256产 地:中国大陆
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T6211PosaconazoleSCH 56592;POS;泊沙康唑
Posaconazole is a sterol C14ɑ demethylase inhibitor (IC50: 0.25 nM).
价 格:¥电议型 号:T6211产 地:中国大陆
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T6177PF-562271 besylatePF-00562271 Besylate
PF-562271 (besylate) is a potent, ATP-competitive, reversible inhibitor of FAK with IC50 of 1.5 nM, ~10-fold less potent for Pyk2 than FAK and >100-fold selectivity against other protein kinases, except for some CDKs.
价 格:¥电议型 号:T6177产 地:中国大陆
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T6156Ruxolitinib (S enantiomer)S-Ruxolitinib;INCB018424;INCB18424;Ruxolitinib S enantiomer;环丙基[4-[3-(1H-咪
Ruxolitinib S enantiomer is the S-enantiomer of Ruxolitinib. Ruxolitinib is the first potent, selective JAK1/2 inhibitor.
价 格:¥电议型 号:T6156产 地:中国大陆