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T16710MericitabineRG 7128;R-7128;PSI 6130 diisobutyrate
Mericitabine is a nucleoside HCV NS5B polymerase inhibitor. It acts as an RNA chain terminator and prevents the elongation of RNA transcripts during replication.
价 格:¥电议型 号:T16710产 地:中国大陆
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T1654Pentamidine isethionatePentamidine isethionate salt;Pentamidine diisethionate;喷他脒羟乙磺酸盐
Pentamidine isethionate is a synthetic amidine derivative, Pentamidine Isethionate is an antiprotozoal and antifungal agent.
价 格:¥电议型 号:T1654产 地:中国大陆
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T1557AcetylspiramycinForomacidin B;Spiramycin B;ASPM;Spiramycin II;乙酰螺旋霉素
Acetylspiramycin targets 50S ribosome to inhibit protein synthesis.
价 格:¥电议型 号:T1557产 地:中国大陆
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T15129DiIDiIC18(3)
DiI is a lipophilic membrane dye. It diffuses laterally to stain the entire cell. DiI is excited to emit orange-red fluorescence which is weak in water but strong and photostable when incorporated into membranes.
价 格:¥电议型 号:T15129产 地:中国大陆
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T14860CaMKII-IN-1
CaMKII-IN-1 is a potent and highly selective inhibitor of CaMKII (IC50 = 63 nM). CaMKII-IN-1 exhibited more than 100-fold higher selectivity for CaMKII over CaMKIV, MLCK, p38a, Akt1, and PKC.
价 格:¥电议型 号:T14860产 地:中国大陆
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T14322ARP-100MMP-2 Inhibitor III;ARP100
ARP-100 is a potent and selective matrix metalloproteinase MMP-2 inhibitor (IC50=12 nM). ARP-100 shows the less inhibitory activity towards MMP-1 (>50 μM), MMP-3 (4.5 μM), MMP-7 (>50 μM), and MMP-9 (0.2 μM)[1][2]. ARP-100 interacts with S1' pocket of MMP-
价 格:¥电议型 号:T14322产 地:中国大陆
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T1408CapecitabineCapecitibine;RO 09-1978;Xeloda;Capiibine;卡培他滨
Capecitabine is a fluoropyrimidine carbamate belonging to the class of antineoplastic agents called antimetabolites. As a prodrug, capecitabine is selectively activated by tumor cells to its cytotoxic moiety, 5-fluorouracil (5-FU); subsequently, 5-FU is m
价 格:¥电议型 号:T1408产 地:中国大陆
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T1383Bitoscanatep-Phenylene diisothiocyanate;PDITC;Biscomate;1,4-Diisothiocyanatobenzene;对苯二异硫氰酸酯
Biscomate is used in the treatment of hookworms.
价 格:¥电议型 号:T1383产 地:中国大陆
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T134923,5-Diiodothyropropionic acid3,5-二碘甲腺丙酸;Ditpa cpd;C082182
3,5-Diiodothyropropionic acid is a thyroid hormone analog. It induces α-myosin heavy chain mRNA expression, binds to thyroid hormone receptor (Ka: 2.40/M and 4.06/M for TRα1 and TRβ1).
价 格:¥电议型 号:T13492产 地:中国大陆
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T13480(S)-(-)-5-Fluorowillardiine5-氟代尿嘧啶丙氨酸;(5S)-Fluorowillardiine;(S)-5-Fluorowillardiine
(S)-(-)-5-Fluorowillardiine is an AMPA receptor-specific agonist
价 格:¥电议型 号:T13480产 地:中国大陆
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T13396Zinc Protoporphyrin锌原卟啉;ZnPP;Zn(II)-protoporphyrin IX;Zinc Protoporphyrin-9
Zinc Protoporphyrin is an orally active and competitive inhibitor of heme oxygenase-1 (HO-1) and markedly attenuates the protective effects of Phloroglucinol (PG) against H2O2, and has anti-cancer activity.
价 格:¥电议型 号:T13396产 地:中国大陆
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T12651Rabdosiin(+)-Rabdosiin
Rabdosiin is a natural product, and has anti-allergic activity, anti-HIV activity and inhibition on DNA topoisomerase.
价 格:¥电议型 号:T12651产 地:中国大陆
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T12469PI4KIIIbeta-IN-9
PI4KIIIbeta-IN-9 is a potent inhibitor of PI4KIIIβ(IC50 of 7 nM). .
价 格:¥电议型 号:T12469产 地:中国大陆
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T12468PI4KIIIbeta-IN-10
PI4KIIIbeta-IN-10 is a potent inhibitor of PI4KIIIβ (IC50 of 3.6 nM).
价 格:¥电议型 号:T12468产 地:中国大陆
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T12058MK2-IN-3 hydrateMK-2 Inhibitor III
MK2-IN-3 hydrate is an orally active, selective, and ATP-competitive inhibitor of MAPKAP-K2 (MK-2) (IC50 of 0.85 nM)
价 格:¥电议型 号:T12058产 地:中国大陆
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T11872LLMP744 hydrochlorideNSC706744 hydrochloride;MJ-III65 hydrochloride
LMP744 hydrochloride is a DNA intercalator and Topoisomerase I (Top1) inhibitor with antitumor activity.?
价 格:¥电议型 号:T11872L产 地:中国大陆
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T11696IvachtinCaspase-3 Inhibitor VII
Ivachtin is a nonpeptide, noncompetitive and reversibl caspase-3 inhibitor(IC50 = 23 nM) and is a modest inhibitor of the remaining caspases.
价 格:¥电议型 号:T11696产 地:中国大陆
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T11563Histone Acetyltransferase Inhibitor II
Histone Acetyltransferase Inhibitor II is a selective and cell permeable inhibitor of p300 histone acetyltransferase(IC50 : 5 μM).with anti-acetylase activity in mammalian cells.
价 格:¥电议型 号:T11563产 地:中国大陆
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T11249LDxdExatecan derivative for ADC;UNII-OQM5SD32BQ;OQM5SD32BQ
Dxd is a potent inhibitor of DNA topoisomerase I with an IC50 of 0.31 μM. It is used as a conjugated drug of HER2-targeting ADC.
价 格:¥电议型 号:T11249L产 地:中国大陆
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T10884CRAC intermediate 15-(S)-Fluorowillardiine
CRAC intermediate 1 is a key intermediate in the chemical synthesis of a series of CRAC channel inhibitors.
价 格:¥电议型 号:T10884产 地:中国大陆