其他產(chǎn)品及廠家

Atractylenolide III白術(shù)內(nèi)酯 III；ICodonolactone；8β-Hydroxyasterolide
atractylenolide iii may have therapeutic potential in treating homocysteine-mediated cognitive impairment and neuronal injury. atractylenolide iii is a potential candidate for the treatment of human lung carcinoma by inducing the release of cytochrome c,
更新時(shí)間:2025-11-04
Angoroside C安格洛甙C；安格洛苷C
angoroside c is a potential anti-inflammatory compound. inhibitor of prostaglandin e2 release in mouse peritoneal macrophages in vitro. shows potent antioxidative activity in reducing the oxidized oh adducts of damp and dgmp. reveals some trypanocidal pot
更新時(shí)間:2025-11-04
Gomisin J
gomisin j is a natural product and have vasodilatory activity. gomisin j suppresses lipid accumulation by regulating the expression of lipogenic and lipolytic enzymes and inflammatory molecules through activation of ampk, lkb1 and ca2+/calmodulin-dependen
更新時(shí)間:2025-11-04
Yubeinine
yubeinine is an alkaloid natural product possessing tracheal relaxant effects.
更新時(shí)間:2025-11-04
Isomangiferin芒果；異芒果苷
isomangiferin has an antiviral effect, may due to their capability of inhibiting virus replication within cells. it also has antioxidant and radical-scavenging activities.
更新時(shí)間:2025-11-04
Epimedin A
epimedin a has anti-osteoporosis activities in vivo.
更新時(shí)間:2025-11-04
TenuigeninSenegin；Senegenin；遠(yuǎn)志皂苷元
senegenin is a natural product from polygala tenuifolia used in chinese medicine with antioxidative and anti-inflammatory activity.
更新時(shí)間:2025-11-04
10-Gingerol[10]-姜酚；10-姜酚
10-gingerol-induced apoptosis was accompanied by phosphorylation of the mitogen-activated protein kinase (mapks) family, p38 mapk (p38), c-jun n-terminal kinase (jnk), and extracellular signal-regulated kinase (erk).
更新時(shí)間:2025-11-04
Pulsatilla saponin D白頭翁皂苷D；Hederacolchiside A；SB365
pulsatilla saponin d has exhibited potential beneficial effects as a chemopreventive agent for critical health conditions including cancer, and it inhibits cell growth via cell cycle arrest and apoptosis in various cancer cell types.
更新時(shí)間:2025-11-04
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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)間:2025-11-04
Neoliquiritin
neoliquiritin may possess ytotoxiciy and tumor-specificity.
更新時(shí)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(shí)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(shí)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(shí)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(shí)間:2025-11-04
Isobavachin
isobavachin can facilitate mouse es cells differentiating into neuronal cells.
更新時(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)間:2025-11-04

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