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T39792AMPC；AMPCAMPC
AMPC, a powerful and efficient inhibitor of TFF3, demonstrates inhibitory effects on cell proliferation, survival, oncogenicity, and CSC-like behavior in TFF3-positive CMS4 CRC cells. It acts as a promising standalone anti-cancer agent and also enhances the effects of 5-FU when used in combination, making it a valuable tool for cancer research.
价 格：￥电议型 号：T39792产 地：中国大陆
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T38696Rp-8-CPT-cAMPS；Rp-8-CPT-cAMPSRp-8-CPT-cAMPS
Rp-8-CPT-cAMPS is a powerful and competitive antagonist of cAMP-induced activation of cAMP-dependent protein kinase (PKA) I and II. Acting as a potent cAMP analog, Rp-8-CPT-cAMPS exhibits a preference for site A of RI over site A of RII. Additionally, it favors site B of RII over site B of RI. This compound effectively inhibits cAMP-dependent PKA activation and demonstrates selectivity in binding to specific sites within the protein kinase.
价 格：￥电议型 号：T38696产 地：中国大陆
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T38694Sp-8-CPT-cAMPS；Sp-8-CPT-cAMPSSp-8-CPT-cAMPS
Sp-8-CPT-cAMPS is a powerful and specific cAMP analog that activates cAMP-dependent protein kinase A (PKA I and PKA II) selectively and effectively. It exhibits a 153-fold preference for site A of RI over site A of RII, and a 59-fold preference for site B of RII over site B of RI.
价 格：￥电议型 号：T38694产 地：中国大陆
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T36679Rp-cAMPS sodium salt；Rp-cAMPS sodium saltRp-cAMPS sodium salt
Rp-cAMPS sodium salt, a cAMP analog, is a potent, competitive cAMP-induced activation of cAMP-dependent PKA I and II (Kis of 12.5 μM and 4.5 μM, respectively) antagonist. Rp-cAMPS sodium salt is resistant to hydrolysis by phosphodiesterases[1][2][3][4][5][6].
价 格：￥电议型 号：T36679产 地：中国大陆
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T36678Rp-8-CPT-cAMPS sodium；Rp-8-CPT-Cyclic AMP (sodium salt)Rp-8-CPT-cAMPS sodium
Rp-8-CPT-cAMP is a structural combination of the lipophilic and non-hydrolyzable cAMP analogs, 8-CPT-cyclic AMP and Rp-cyclic AMPS .[1] It functions as a site-selective inhibitor of protein kinase A (PKA) type I and II, with preference towards site A of type I and site B of type II.2 By occupying cAMP binding sites at the regulatory subunit of PKA, Rp-8-CPT-cAMP prevents the kinase holoenzyme from dissociative activation.[2],[3]
价 格：￥电议型 号：T36678产 地：中国大陆
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T34895Tocamphyl；化合物 T34895Tocanfil|||Biliphorin|||Gallogen；Tocanfil|||Biliphorin|||Gallogen
Tocamphyl is a cholagogic agent that stimulates pancreatic exocrine and bile flow when administered in the duodenum.
价 格：￥电议型 号：T34895产 地：中国大陆
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T30788Cefoperasone mixture with sulbactam；化合物 T30788Bacamp|||Sulperazone|||Cefactam|||Jincetam；Bacamp|||Su
Cefoperasone mixture with sulbactam is a bioactive chemical.
价 格：￥电议型 号：T30788产 地：中国大陆
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T30475Bismuth camphocarbonate；化合物 T30475Bi-Valeas|||Solmuth|||Cardyl|||Rectobismutina|||Angimuth；Bi-Valeas
Bismuth camphocarbonate is used for herpes zoster.
价 格：￥电议型 号：T30475产 地：中国大陆
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T30048Anemonin (6CI)；化合物 T30048Pulsatilla camphor|||Anemonin|||Anemone camphor；Pulsatilla camphor|||Anemon
Anemonin is a furanone dimer found in the Buttercup (Ranunculaceae) family. Anemonin has been shown to regulate tyrosinase-related proteins and mRNA in human melanocytes and may be useful in attenuting osteoarthritis progression.
价 格：￥电议型 号：T30048产 地：中国大陆
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T2952Camphor；樟脑(±)-Camphor|||Bornan-2-one|||2-Camphanone|||2-Bornanone|||Formosa；樟脑|||(±)-Camphor|||Borna
Camphor (2-Camphanone) is a bicyclic monoterpene ketone found widely in plants, especially CINNAMOMUM CAMPHORA. It is used topically as a skin antipruritic and as an anti-infective agent.
价 格：￥电议型 号：T2952产 地：中国大陆
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T2916Patchouli alcohol；百秋李醇Patchouli camphor|||Patchoulol|||(-)-Patchouli Alcohol；百秋李醇|||Patchouli campho
Patchouli alcohol (Patchoulol) is a sesquiterpene alcohol found in patchouli oil. It has antibacterial, antifungal, and antiviral actions. Patchouli alcohol also suppresses inflammation induced by lipopolysaccharide in vivo. Topical application of patchouli alcohol accelerates recovery from ultraviolet irradiation-induced skin damage through antioxidant and anti-inflammatory effects.
价 格：￥电议型 号：T2916产 地：中国大陆
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T28990Tocladesine；化合物 T28990NSC-614491|||CN 1256|||CN1256|||8-Cl-cAMP|||NSC614491|||ICN-1256；NSC-614491|||
Tocladesine, a cyclic adenosine monophosphate (cAMP) receptor agonist, is used potentially for the treatment of colorectal cancer.
价 格：￥电议型 号：T28990产 地：中国大陆
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T2896Alantolactone；土木香内酯helenin|||Eupatal|||Helenine|||(+)-Alantolactone|||Alant camphor|||Inula camphor；
Alantolactone (Inula camphor)(Alant camphor), a sesquiterpene lactone, has potential activity against triple-negative breast Y MDA-MB-231 cells by suppressing the signal transducer and activator of transcription 3 (STAT3) signaling pathway.
价 格：￥电议型 号：T2896产 地：中国大陆
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T28615Sp-cAMPS；化合物 T28615Rp-cAMPS TEA|||Rp cAMPS TEA|||Rp-cAMPS TEA salt|||Rp cAMPS TEA salt；Rp-cAMPS TEA|
Rp-cAMPS TEA salt is a cAMP-dependent protein kinase (PKA) activator.
价 格：￥电议型 号：T28615产 地：中国大陆
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T2764(S)-10-Hydroxycamptothecin；10-羟基喜树碱10-Hydroxycamptothecin|||10-HCPT；10-羟喜树碱|||10-羟基喜树碱|||10-Hydroxyc
(S)-10-Hydroxycamptothecin (10-HCPT) is a DNA topoisomerase I inhibitor, utilized as a clinical therapy agent against hepatoma.
价 格：￥电议型 号：T2764产 地：中国大陆
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T27113Camptothecin-20(S)-O-propionate；化合物 T27113CZ 48|||CZ48|||CZ-48；CZ 48|||CZ48|||CZ-48
CZ-48 is a DNA topoisomerase inhibitor.
价 格：￥电议型 号：T27113产 地：中国大陆
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T24610Pegamotecan；化合物PegamotecanProthecan|||PEG-camptothecin|||PEG-beta-CPT；Prothecan|||PEG-camptothecin||
Pegamotecan (PEG-camptothecin) is a topoisomerase I (TOP1) inhibitor with anticancer activity, and it is used in the treatment of esophageal, non-small cell lung and pancreatic cancers.
价 格：￥电议型 号：T24610产 地：中国大陆
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T22621Rp-cAMPS；化合物 T22621cAMPS-Sp, triethylammonium salt；cAMPS-Sp, triethylammonium salt
Rp-cAMPS competitively inhibits the cAMP-induced activation of cAMP-dependent protein kinase (PKA).
价 格：￥电议型 号：T22621产 地：中国大陆
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T225368-pCPT-2-O-Me-cAMP-AM；化合物 T225368 pCPT 2 O Me cAMP AM|||8-pCPT-2-O-Me-cAMP-AM|||8pCPT2OMecAMPAM；8 pC
Epac activator
价 格：￥电议型 号：T22536产 地：中国大陆
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T225296-Bnz-cAMP sodium salt；化合物 T225296-Bnz-cAMP sodium salt
6-Bnz-cAMP is a PKA-selective activator. It regulates the PKA dependent signaling pathways. The proliferative signaling pathway which activated by the 6-Bnz-cAMP involves activation of the epidermal growth factor receptor and ERK1/2. Extending the duration of PKA-dependent ERK1/2 activation and converted cAMP from a proliferative into an anti-proliferative, neurite outgrowth- promoting signal.
价 格：￥电议型 号：T22529产 地：中国大陆
