其他產(chǎn)品及廠家

Pulchinenoside A白頭翁皂苷A；Anemoside A3
anemoside a3 is an attractive candidate for further development as a cognitive enhancer capable of alleviating memory dysfunctions associated with aging and neurodegenerative diseases.
更新時間:2025-11-04
Saikosaponin B1柴胡皂苷B1；柴胡皂苷 B1
saponin activator. activates release of prostaglandin e2 in vitro. anti-inflammatory agent. orally active. active in vivo and in vitro.
更新時間:2025-11-04
Saikosaponin D
saikosaponin d is a novel serca inhibitor by inhibiting nf-κb and stat3 signaling to protect against acetaminophen-induced hepatotoxicity.
更新時間:2025-11-04
Saikosaponin C柴胡皂苷C；柴胡皂苷 C
saikosaponin c efficiently inhibited lps-induced apoptotic cell death via inhibition of caspase-3 activation and caspase-3-mediated-fak degradation.
更新時間:2025-11-04
Ginsenoside RoPolysciasaponin P3；Chikusetsusaponin V；Chikusetsusaponin 5；人參皂苷Ro；人參皂苷 Ro
ginsenosidero exhibits a ca2+-antagonistic antiplatelet effect.
更新時間:2025-11-04
Ginsenoside F2人參皂苷F2
ginsenoside f2 has antiproliferative activity against breast cancer stem cells (cscs). it induces apoptosis in breast cscs by activating the intrinsic apoptotic pathway and mitochondrial dysfunction.
更新時間:2025-11-04
Ro60-0175Ro60-0175
ro60-0175 is a potent and selective agonist of 5-ht 2c receptor. ro60-0175 reduces cocaine self-administration, and the ability of cocaine to reinstate responding after extinction of drug-seeking behavior.
更新時間:2025-11-04
Protopanaxatriol原人參三醇；20(R)-Protopanaxatriol；20(R)-APPT；(20R)-Protopanaxatriol
protopanaxatriol, a major ginseng constituent, is a novel pparγ antagonist.
更新時間:2025-11-04
Ginsenoside Rb3人參皂苷 Rb3；人參皂苷Rb3；Gypenoside IV
ginsenoside rb3 is a natural triterpenoid saponin, exhibiting inhibition effect on tnfα-induced nf-κb transcriptional activity. it also inhibits the induction of cox-2 and inos mrna.
更新時間:2025-11-04
Ginsenoside Rb2人參皂苷 Rb2；人參皂苷Rb2；Ginsenoside C
ginsenoside rb2 found in species of panax, upregulating gpr120 gene expression.
更新時間:2025-11-04
DSTYSLSSTLTLSK acetate
dstyslsstltlsk acetate is a human generic peptide that can be used for the quantitative detection of infliximab.
更新時間:2025-11-04
Pseudoginsenoside F11Ginsenoside A1；擬人參皂苷 F11；擬人參皂苷F11
pseudoginsenoside-f11 is a component of panax quinquefolium (american ginseng), can antagonize the learning and memory deficits induced by scopolamine, morphine, and methamphetamine in mice.
更新時間:2025-11-04
CZC-54252 hydrochloride
czc-54252 hydrochloride is a potent and selective lrrk2 inhibitor with ic 50 s of 1.28 nm and 1.85 nm for wild-type and g2019s lrrk2 , respectively. g2019s lrrk2 -induced human neuronal injury is attenuated by czc-54252 hydrochloride with an ec 50 of ~1 n
更新時間:2025-11-04
Punicalagin安石榴甙；安石榴苷
punicalagin is a major ellagitannin found in pomegranates that is reported to produce antioxidant, anti-inflammatory, and anticancer effects. it has been shown to prevent high-fat diet-induced obesity-associated accumulation of cardiac triglyceride and ch
更新時間:2025-11-04
SIRT7 inhibitor 97491
sirt7 inhibitor 97491 is an hdac inhibitor with high specificity for sirt7 (ic50 = 325 nm). sirt7 inhibitor 97491 promotes apoptosis through caspase pathway.
更新時間:2025-11-04
Astragaloside IIAstrasieversianin VIII；黃芪皂苷 II
astragaloside ii is an effective mdr reversal agent and may be a potential adjunctive agent for hepatic cancer chemotherapy. astragaloside ii also induces osteogenic activities, differentiation, proliferation, and mineralization, through the bone morphoge
更新時間:2025-11-04
Astragaloside I黃芪皂苷I；Cyclosieversioside B；Astrasieversianin IV
astragaloside i is a natural product isolated from astragalus.
更新時間:2025-11-04
Bevurogant
bevurogant is a retinoid-related orphan receptor-gamma t (rorγt) antagonist. bevurogant can be used for the research of chronic inflammatory diseases.
更新時間:2025-11-04
EchinatinRetrochalcone；刺甘草查爾酮
echinatin disturb the mitochondrial energy transfer reactions and membrane permeability, at a low concentration cause deterioration of respiratory control and oxidative phosphorylation of isolated rat liver mitochondria, inhibits dnp-atpase activity while
更新時間:2025-11-04
BIM-23190 aceate
bim-23190 aceate, a somatostatin analog, a selective agonist of sstr2 and sstr5. bim-23190 can be used in cancer and acromegaly studies.
更新時間:2025-11-04
Azido-PEG4-azideAzido-PEG4-azide
azido-peg4-azide is a peg-based protac linker that can be used to synthesize protacs.
更新時間:2025-11-04
Phellopterin
phellopterin is a partial agonist of the central benzodiazepine receptors in vitro. phellopterin shows a cytotoxic effect on raw264.7 cell at the concentration from 40 to 400 μm. phellopterin reduce tnf-alpha-induced vcam-1 expression through regulation o
更新時間:2025-11-04
BefotertinibD-0316；Befotertinib
befotertinib (d-0316) is the third-generation egfr tyrosine kinase inhibitor. befotertinib can be used for the research of egfr t790m-positive non-small cell lung cancer (nsclc).
更新時間:2025-11-04
Neoliquiritin
neoliquiritin may possess ytotoxiciy and tumor-specificity.
更新時間:2025-11-04
Nitrofen
nitrofen is a selective contact herbicide. nitrofen is a retinal dehydrogenase and protoporphyrinogen oxidase inhibitor [1] [2] .
更新時間:2025-11-04
EST73502
est73502 is an agonist of μ-opioid receptor(ki = 64 nm) agonist and an antagonist of σ1 receptor (ki = 118 nm). est73502 displays antinociceptive activity.
更新時間:2025-11-04
Kaurenoic acid異貝殼杉烯酸；kaur-16-en-18-oic acid；Kauren-19-Oic Acid；kaurenoate
kaurenoic acid has anti-inflammatory potential in acetic acid-induced colitis, decreases in mda level. kaurenoic acid exerts a uterine relaxant effect acting principally through calcium blockade and in part, by the opening of atp-sensitive potassium chann
更新時間:2025-11-04
Boc-Asp(OMe)-fluoromethyl ketoneBoc-Asp(OMe)-FMK；Boc-Asp(OMe)-fluoromethyl ketone
boc-asp(ome)-fluoromethyl ketone is a broad range caspase inhibitor that inhibits fas-mediated phagocytosis and oxidative rupture inhibition, but does not affect the chemotactic activity of il-8 [1] [2] .
更新時間:2025-11-04
Isobavachin
isobavachin can facilitate mouse es cells differentiating into neuronal cells.
更新時間:2025-11-04
Jatrorrhizine藥根堿；neprotin；Yatrorizine
jatrorrhizine is a protoberberine alkaloid isolated from enantia chlorantha (annonaceae) and other species. it was found to have antimicrobial and antifungal activity. it binds and noncompetitively inhibits monoamine oxidase (ic50 4 micromolar for mao-a a
更新時間:2025-11-04
Isavuconazonium sulfate
isavuconazonium sulfate is hydrolyzed by plasma esterases to yield the active moiety isavuconazole. isavuconazole binds to and inhibits the fungal cytochrome p450 family enzyme lanosterol 14-alpha-demethylase (cyp51), which catalyzes the demethylation of
更新時間:2025-11-04
γ-Glu-Gly acetate
γ-glu-gly aceate is a human lipid metabolite that is acetate for γ-glutamine dipeptide.
更新時間:2025-11-04
PATULIN散毒素；棒曲霉素；Claviform；Clavacin；Expansin
patulin is a mycotoxin produced by a variety of molds commonly found in rotting apples, including aspergillus and penicillium.
更新時間:2025-11-04
Methyl L-histidinate dihydrochlorideL-組氨酸甲酯二鹽酸鹽；L-Histidine methyl ester dihydrochloride
inhibition of histidine decarboxylase in sprague-dawley rat stomach assessed as decrease in 14co2 production with activty value of 1.8 μm
更新時間:2025-11-04
H-HomoArg-OH.HClL-高精氨酸鹽酸鹽；L-Homoarginine hydrochloride；NSC 145416；L(+)-Homoarginine hydrochloride
l-homoarginine is a specific inhibitor of liver-type alkaline phosphatase.
更新時間:2025-11-04
BenzoinBenzoylphenylcarbinol；安息香
the main uses of benzoin are as a precursor to benzil, which is a photoinitiator.
更新時間:2025-11-04
C-Type Natriuretic Peptide (CNP) (1-22), human acetateC-Type Natriuretic Peptide (CNP) (1-22), human
c-type natriuretic peptide (cnp) (1-22), human acetate is an agonist of natriuretic peptide receptor b (npr-b), an endothelial-derived relaxant and growth inhibitory factor. c-type natriuretic peptide (cnp) (1-22), human acetate inhibits camp synthesis s
更新時間:2025-11-04
CID5721353BCL6 inhibitor
cid5721353 is a b-cell lymphoma 6 inhibitor (bcl6 inhibitor) that disrupts bcl6/corepressor complexes in vitro and in vivo, and was shown to bind the critical site within the btb groove.
更新時間:2025-11-04
Choline Fenofibrate非諾貝特膽堿；Trilipix；ABT-335
choline fenofibrate is a choline formulation of fenofibrate, a synthetic phenoxy-isobutyric acid derivate and prodrug with antihyperlipidemic activity.
更新時間:2025-11-04
RadiprodilRGH-896
radiprodil (rgh-896) is an orally active and selective nmda nr2b receptors antagonist. it was a potential treatment of neuropathic pain associated with diabetic peripheral neuropathy (dpnp).
更新時間:2025-11-04
Asapiprant
asapiprant (s-555739) is a potent and selective dp1 receptor antagonist (ki: 0.44 nm). it exhibited high affinity and selectivity for the dp1 receptor.
更新時間:2025-11-04
lp-211 is a brain penetrant selective agonist for a 5-ht7 receptor (ki: 0.58 nm), and >300-fold selectivity over the 5-ht1a receptor.
更新時間:2025-11-04
2,5-PYRIDINEDICARBOXYLIC ACID
2,5-pyridinedicarboxylic acid is used in the preparation of new derivatives as antiviral agents.
更新時間:2025-11-04
Volinanserin氟利色林；MDL100907；M 100907
volinanserin (mdl 100907) is a potent and selective antagonist of the serotonin receptor 5-ht2 (ki: 0.36 nm) and shows 300-fold selectivity for 5-ht2 receptor over 5-ht1c, alpha-1 adrenergic and sigma receptors.
更新時間:2025-11-04
Bepridil hydrochlorideCERM 1978；鹽酸芐普地爾
bepridil is a calcium channel blocker and also inhibits na+/ca2+ exchange (ncx), sodium channels and cardiac sarcolemmal katp channels.
更新時間:2025-11-04
TP0463518
tp-0463518 is a highly potent hif prolyl hydroxylase (phd) inhibitor (ic50s: 13 nm and 18 nm for human and rat phd2, respectively).
更新時間:2025-11-04
CK1-IN-1PUN51207
ck1-in-1, compound 1c reported in patent wo2015119579a1, is a casein kinase 1 (ck1) inhibitor. it has ic50s of 15 nm, 16 nm, 73 nm for ck1δ, and ck1ε, p38σ mapk, respectively.
更新時間:2025-11-04
Prulifloxacin普盧利沙星；Pruvel；NM441；AF 3012
prulifloxacin is a broad-spectrum fluoroquinolone antibiotic. it inhibits bacterial dna synthesis by inhibiting the activity of bacterial dna topoisomerase ii and iv.
更新時間:2025-11-04
BSJ-03-123
bsj-03-123 is a potent, cdk6-selective small-molecule degrader.
更新時間:2025-11-04

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