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G1

Products for  G1

  1. Cat.No. Product Name Information
  2. GC40675 2-deoxy-Artemisinin 2-deoxy-Artemisinin is an inactive metabolite of the antimalarial agent artemisinin. 2-deoxy-Artemisinin  Chemical Structure
  3. GC45354 4β-Hydroxywithanolide E A withanolide with anti-inflammatory and anticancer activities 4β-Hydroxywithanolide E  Chemical Structure
  4. GC42586 6α-hydroxy Paclitaxel 6α-hydroxy Paclitaxel is a primary metabolite of the anticancer compound paclitaxel, produced by the action of the cytochrome P450 isoform CYP2C8. 6α-hydroxy Paclitaxel  Chemical Structure
  5. GC49393 all-trans-13,14-Dihydroretinol A metabolite of all-trans retinoic acid all-trans-13,14-Dihydroretinol  Chemical Structure
  6. GC18539 all-trans-4-hydroxy Retinoic Acid all-trans-4-hydroxy Retinoic acid is a metabolite of all-trans retinoic acid formed by the cytochrome P450 (CYP) isoforms CYP26A1, B1, and C1. all-trans-4-hydroxy Retinoic Acid  Chemical Structure
  7. GC45385 Ara-G   Ara-G  Chemical Structure
  8. GC46882 Artemisinin-d3 An internal standard for the quantification of artemisinin Artemisinin-d3  Chemical Structure
  9. GC49042 Benastatin A A bacterial metabolite with diverse biological activities Benastatin A  Chemical Structure
  10. GC40009 Bostrycin Bostrycin is an anthraquinone originally isolated from B. Bostrycin  Chemical Structure
  11. GC40708 C2 L-erythro Ceramide (d18:1/2:0) C2 L-erythro Ceramide is a bioactive sphingolipid and a cell-permeable analog of naturally occurring ceramides. C2 L-erythro Ceramide (d18:1/2:0)  Chemical Structure
  12. GC40709 C2 L-threo Ceramide (d18:1/2:0) C2 L-threo Ceramide is a bioactive sphingolipid and cell-permeable analog of naturally occurring ceramides. C2 L-threo Ceramide (d18:1/2:0)  Chemical Structure
  13. GC40795 CAY10503 CAY10503 is a proapoptotic, antiproliferative compound that is able to arrest cell cycle progression in the G0-G1 phase. CAY10503  Chemical Structure
  14. GC52245 CAY10792 An anticancer agent CAY10792  Chemical Structure
  15. GC43217 CDK/CRK Inhibitor CDK/CRK inhibitor is an inhibitor of cyclin-dependent kinases (CDK) and CDK-related kinases (CRK) with IC50 values ranging from 9-839 nM in vitro. CDK/CRK Inhibitor  Chemical Structure
  16. GC43265 Chromomycin A2 Chromomycin A2 is an aureolic acid that has been found in several marine actinomycetes and has antibacterial and anticancer activities. Chromomycin A2  Chemical Structure
  17. GC43354 Cysmethynil Post-translational protein prenylation is a 3-step process that occurs at the C-terminus of a number of proteins involved in cell growth control and oncogenesis. Cysmethynil  Chemical Structure
  18. GC40296 D-erythro-MAPP D-erythro-MAPP is a derivative of ceramide and an inhibitor of alkaline ceramidase (Ki = 2-13 μM; IC50 = 1-5 μM). D-erythro-MAPP  Chemical Structure
  19. GC18693 Fascaplysin (chloride) Fascaplysin (chloride) is an antimicrobial and cytotoxic red pigment, that can come from the marine sponge (Fascaplysin (chloride)opsis sp. Fascaplysin (chloride)  Chemical Structure
  20. GC49344 Fisetin-d5 An internal standard for the quantification of fisetin Fisetin-d5  Chemical Structure
  21. GC49089 FR900359 A cyclic depsipeptide and an inhibitor of Gαq, Gα11, and Gα14<•sub> FR900359  Chemical Structure
  22. GC48387 Inostamycin A A bacterial metabolite with anticancer activity Inostamycin A  Chemical Structure
  23. GC52472 Inostamycin A (sodium salt) A bacterial metabolite with anticancer activity Inostamycin A (sodium salt)  Chemical Structure
  24. GC43995 Kazusamycin B Kazusamycin B is a bacterial metabolite originally isolated from Streptomyces. Kazusamycin B  Chemical Structure
  25. GC47619 Menaquinone 4-d7 An internal standard for the quantification of menaquinone 4 Menaquinone 4-d7  Chemical Structure
  26. GC45523 Nemorosone   Nemorosone  Chemical Structure
  27. GC45538 Oxychlororaphine   Oxychlororaphine  Chemical Structure
  28. GA23337 Oxythiamine . HCl Thiamine antagonist and inhibitor of saccharomyces cerevisiae transketolase. RaÏs et al. indicated that oxythiamine inhibits the growth of Ehrlich's tumor cells. Oxythiamine . HCl  Chemical Structure
  29. GC45758 Paclitaxel octadecanedioate A prodrug form of paclitaxel Paclitaxel octadecanedioate  Chemical Structure
  30. GC47853 Paclitaxel-d5 An internal standard for the quantification of paclitaxel Paclitaxel-d5  Chemical Structure
  31. GC18353 Prostaglandin A2 A naturally occurring prostaglandin with antiviral/antitumor activity Prostaglandin A2  Chemical Structure
  32. GC48019 Quercetin (hydrate) A flavonoid with diverse biological activities Quercetin (hydrate)  Chemical Structure
  33. GC44846 RK-682 (calcium salt) Protein tyrosine phosphatases (PTPs) remove phosphate from tyrosine residues of cellular proteins. RK-682 (calcium salt)  Chemical Structure
  34. GC18852 S14161 D-Cyclins regulate the cell cycle by acting in a complex with cyclin dependent kinases (CDKs) to promote phosphorylation of the retinoblastoma protein and initiate cellular progression from the G1 to the S phase. S14161  Chemical Structure
  35. GC49674 Schizandrin Schizandrin (Schizandrin), a dibenzocyclooctadiene lignan, is isolated from the fruit of Schisandra chinensis Baill. Schizandrin  Chemical Structure
  36. GC48076 Sesquicillin A A fungal metabolite Sesquicillin A  Chemical Structure
  37. GC49002 Sinigrin (hydrate) A glucosinolate with diverse biological activities Sinigrin (hydrate)  Chemical Structure
  38. GC48659 Umbelliprenin A prenylated coumarin with diverse biological activities Umbelliprenin  Chemical Structure
  39. GC40044 Zymostenol Zymostenol is a late-stage precursor in the biosynthesis of cholesterol. Zymostenol  Chemical Structure

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