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T8995NCGC00262650NCGC00262650,inhibit,Inhibitor,apical membrane antigen 1,AMA1-RON2,merozoites,NCGC 00262
NCGC00262650 is an inhibitor of AMA1-RON2 interaction and c-Src tyrosine kinase activity.
价 格：￥电议型 号：T8995产 地：中国大陆
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TN2356TetradehydropodophyllotoxinInhibitor,Fungal,Tetradehydropodophyllotoxin,inhibit
Tetradehydropodophyllotoxin has anti-tumor activity.
价 格：￥电议型 号：TN2356产 地：中国大陆
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T61233Penehyclidine hydrochloride
Penehyclidine hydrochloride is an?M1?and?M3?antagonist and activates?NF-κB?in lung tissue. Penehyclidine hydrochloride inhibits the release of inflammatory factors and shows anticholinergic properties.
价 格：￥电议型 号：T61233产 地：中国大陆
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T16831(S)-SNAP5114(S)SNAP5114,(S)-SNAP-5114,(S) SNAP5114
(S)-SNAP5114 is a selective inhibitor of GABA transport with IC50s of 5 μM for hGAT-3 and 21 μM for rGAT-2. (S)-SNAP5114 has anticonvulsant properties.
价 格：￥电议型 号：T16831产 地：中国大陆
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T9943(E)-6-(4-methylbenzylidene)-5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid(E)6(4methylbenzyli
(E)-6-(4-methylbenzylidene)-5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid is a 2-?benzylidene tetrahydronaphthone derivative and can be used as a firefly luciferase inhibitor in kit.
价 格：￥电议型 号：T9943产 地：中国大陆
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T6741SPDPSPDP,ADC Linkers,Antibody-drug conjugates linkers,inhibit,Inhibitor
SPDP is a short-chain crosslinker, which is used for amine-to-sulfhydryl conjugation via NHS-ester and pyridyldithiol reactive groups that form cleavable (reducible) disulfide bonds with cysteine sulfhydryls. SPDP could activate equal amounts of anti-CD11c and anti-CTLA-4 Abs (in borate buffered saline; pH 8.5).
价 格：￥电议型 号：T6741产 地：中国大陆
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T7968DazoxibenDazoxiben,Inhibitor,inhibit
Dazoxiben is a potent inhibitor of thromboxane (TX) synthase
价 格：￥电议型 号：T7968产 地：中国大陆
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T60757SB-216
SB-216 is able to be used for the research of cancer which is a potent inhibitor of tubulin polymerization. SB-216 exhibits strong antiproliferative potency in a panel of human cancer cell lines, including melanoma, breast cancer, and lung cancer [1].
价 格：￥电议型 号：T60757产 地：中国大陆
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T37891LGLP-1(32-36)amide acetate
GLP-1(32-36)amide acetate is a pentapeptide and derived from the C terminus of the glucoregulatory hormone GLP-1. GLP-1(32-36)amide acetate could inhibit weight gain and modulate whole body glucose metabolism in diabetic mice.
价 格：￥电议型 号：T37891L产 地：中国大陆
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TN6832SulcatoneInhibitor,inhibit,Endogenous Metabolite,Sulcatone
6-Methyl-5-hepten-2-one is an alarm/panic pheromone produce by ant species.
价 格：￥电议型 号：TN6832产 地：中国大陆
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T6424Bromfenac SodiumInhibitor,inhibit,Bromfenac,Cyclooxygenase,HLEC-B3,Bromfenac Sodium,COX,ocular infla
Bromfenac Sodium is a nonsteroidal anti-inflammatory drug (NSAID), which has anti-inflammatory activity and may block prostaglandin synthesis by inhibiting cyclooxygenase 1 and 2.
价 格：￥电议型 号：T6424产 地：中国大陆
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T6386Ampicillin sodiumAmpicillin sodium,Antibiotic,inhibit,Inhibitor,Bacterial,Ampicillin
Ampicillin Sodium is the sodium salt form of ampicillin, a broad-spectrum semisynthetic derivative of aminopenicillin. Ampicillin sodium inhibits bacterial cell wall synthesis by binding to penicillin binding proteins, thereby inhibiting peptidoglycan synthesis, a critical component of the bacterial cell wall.
价 格：￥电议型 号：T6386产 地：中国大陆
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T67844RBN-3143RBN3143
RBN-3143 is a potent and inhibitor of NAD+-competitive catalytic PARP14 (IC50= 4 nM). RBN-3143 inhibits ADP-ribosylation mediated by PARP14 and stabilizes PARP14 in cell lines. RBN-3143 exhibits research potential of lung inflammation.
价 格：￥电议型 号：T67844产 地：中国大陆
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T6410Bexarotenecutaneous,lymphoma,selective,?retinoid,inhibit,Retinoic acid receptors,antineoplastic,T-ce
Bexarotene is a retinoid analogue that is used to treat the skin manifestations of cutaneous T cell lymphoma (CTCL).
价 格：￥电议型 号：T6410产 地：中国大陆
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T7127DC260126stress,DC260126,DC-260126,FFAR,Inhibitor,insulin,inhibit,secretion,Apoptosis,DC 260126,Free
DC260126 is a small-molecule antagonist of FFA1 (GPR40)
价 格：￥电议型 号：T7127产 地：中国大陆
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T10436AZD4573AZD 4573,inhibit,CDK,AZD4573,AZD-4573,Inhibitor,Cyclin dependent kinase
AZD4573 is an effective and selective CDK9 inhibitor (IC50: <4 nM). It enables transient target engagement for the treatment of hematologic malignancies.
价 格：￥电议型 号：T10436产 地：中国大陆
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T101886RK736RK-73,6RK73
6RK73 is a covalent irreversible and specific UCHL1 inhibitor (IC50: 0.23 ?M). 6RK73 shows almost no inhibition of UCHL3 (IC50: 236 ?M).
价 格：￥电议型 号：T10188产 地：中国大陆
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T27026LCJ-13,610 hydrochlorideCJ 13,610 hydrochloride,CJ13,610 hydrochloride
CJ-13,610 hydrochloride is an orally active nonredox-type inhibitor of 5-LOX and can be used in studies about the prevention of untoward pathophysiological effects of LTs.
价 格：￥电议型 号：T27026L产 地：中国大陆
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T12569LPSB-12379 ditriethylamine saltPSB 12379 disodium,PSB12379 disodium
PSB-12379 ditriethylamine salt, a nucleotide analogue, is a potent Ecto-5´-Nucleotidase (CD73) inhibitor with Kis of 9.03 nM (rat) and 2.21 nM (human).
价 格：￥电议型 号：T12569L产 地：中国大陆
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TQ0050NCGC00244536NCGC 00244536,inhibit,Histone Demethylase,NCGC00244536,Inhibitor,NCGC-00244536
NCGC00244536 is a potent KDM4B inhibitor (IC50: 10 nM).
价 格：￥电议型 号：TQ0050产 地：中国大陆
