Found 1428 Aldrich available compounds.
ID Name Structure Top 10 Available References (order by impact factor) Molecular Target(s)
1Compound ID:2
Activity Tested(uM): 35.73

NSC#:25149 Cell Data(>1uM)


C20H30O2    302.45

1:  Vogel BS, Wildung MR, Vogel G, Croteau R.
Abietadiene synthase from grand fir (Abies grandis). cDNA isolation, characterization, and bacterial expression of a bifunctional diterpene cyclase involved in resin acid biosynthesis.
J Biol Chem.    impact factor:   7.666
1996;  271(38): 23262-8

2:  Imaizumi Y, Sakamoto K, Yamada A, Hotta A, Ohya S, Muraki K, Uchiyama M, Ohwada T.
Molecular basis of pimarane compounds as novel activators of large-conductance Ca(2+)-activated K(+) channel alpha-subunit.
Mol Pharmacol.    impact factor:   5.465
2002;  62(4): 836-46

3:  Peters RJ, Flory JE, Jetter R, Ravn MM, Lee HJ, Coates RM, Croteau RB.
Abietadiene synthase from grand fir (Abies grandis): characterization and mechanism of action of the "pseudomature" recombinant enzyme.
Biochemistry.    impact factor:   4.493
2000;  39(50): 15592-602

4:  Funk C, Lewinsohn E, Vogel BS, Steele CL, Croteau R.
Regulation of Oleoresinosis in Grand Fir (Abies grandis) (Coordinate Induction of Monoterpene and Diterpene Cyclases and Two Cytochrome P450-Dependent Diterpenoid Hydroxylases by Stem Wounding).
Plant Physiol.    impact factor:   4.434
1994;  106(3): 999-1005

5:  Cross BE, Myers PL.
The bacterial transformation of abietic acid.
Biochem J.    impact factor:   4.349
1968;  108(2): 303-10

2Compound ID:3

C12H14N2O2    218.25

1:  Richou R, Lallouette P, Richou H.
[Contribution to the study of the modifications of inflammatory reactions, induced by abrine, in guinea pigs immunized with ana-abrine]
C R Acad Sci Hebd Seances Acad Sci D.    impact factor:   0
1966;  263(3): 308-9

3Compound ID:4
Activity Tested(uM): 100

NSC#:148832 Cell Data(>1uM)


C15H20O4    264.32

1:  Abe H, Urao T, Ito T, Seki M, Shinozaki K, Yamaguchi-Shinozaki K.
Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) Function as Transcriptional Activators in Abscisic Acid Signaling.
Plant Cell.    impact factor:   10.463
2003;  15(1): 63-78

2:  Casaretto J, Ho TH.
The Transcription Factors HvABI5 and HvVP1 Are Required for the Abscisic Acid Induction of Gene Expression in Barley Aleurone Cells.
Plant Cell.    impact factor:   10.463
2003;  15(1): 271-84

3:  Zhu J, Gong Z, Zhang C, Song CP, Damsz B, Inan G, Koiwa H, Zhu JK, Hasegawa PM, Bressan RA.
OSM1/SYP61: a syntaxin protein in Arabidopsis controls abscisic acid-mediated and non-abscisic acid-mediated responses to abiotic stress.
Plant Cell.    impact factor:   10.463
2002;  14(12): 3009-28

4:  Jung JY, Kim YW, Kwak JM, Hwang JU, Young J, Schroeder JI, Hwang I, Lee Y.
Phosphatidylinositol 3- and 4-phosphate are required for normal stomatal movements.
Plant Cell.    impact factor:   10.463
2002;  14(10): 2399-412

5:  Zheng ZL, Nafisi M, Tam A, Li H, Crowell DN, Chary SN, Schroeder JI, Shen J, Yang Z.
Plasma membrane-associated ROP10 small GTPase is a specific negative regulator of abscisic acid responses in Arabidopsis.
Plant Cell.    impact factor:   10.463
2002;  14(11): 2787-97

4Compound ID:6

C16H12O5    284.27

1:  Boege F, Straub T, Kehr A, Boesenberg C, Christiansen K, Andersen A, Jakob F, Kohrle J.
Selected novel flavones inhibit the DNA binding or the DNA religation step of eukaryotic topoisomerase I.
J Biol Chem.    impact factor:   7.666
1996;  271(4): 2262-70

2:  Fiorani M, De Sanctis R, De Bellis R, Dacha M.
Intracellular flavonoids as electron donors for extracellular ferricyanide reduction in human erythrocytes.
Free Radic Biol Med.    impact factor:   4.116
2002;  32(1): 64-72

3:  Chen YT, Zheng RL, Jia ZJ, Ju Y.
Flavonoids as superoxide scavengers and antioxidants.
Free Radic Biol Med.    impact factor:   4.116
1990;  9(1): 19-21

4:  Wenzel U, Kuntz S, Daniel H.
Flavonoids with epidermal growth factor-receptor tyrosine kinase inhibitory activity stimulate PEPT1-mediated cefixime uptake into human intestinal epithelial cells.
J Pharmacol Exp Ther.    impact factor:   3.3
2001;  299(1): 351-7

5:  Bylka W, Franski R, Stobiecki M.
Differentiation between isomeric acacetin-6-C-(6"-O-malonyl)glucoside and acacetin-8-C-(6"-O-malonyl)glucoside by using low-energy CID mass spectra.
J Mass Spectrom.    impact factor:   3.167
2002;  37(6): 648-50

5Compound ID:20

C7H16O2    132.2

1:  Guindon Y, Ogilvie WW, Bordeleau J, Cui WL, Durkin K, Gorys V, Juteau H, Lemieux R, Liotta D, Simoneau B, Yoakim C.
Opening of Tartrate Acetals Using Dialkylboron Bromide: Evidence for Stereoselectivity Downstream from Ring Fission.
J Am Chem Soc.    impact factor:   5.537
2003;  125(2): 428-436

2:  Valahovic MT, Gunnoe TB, Sabat M, Harman WD.
Ligand-modulated stereo- and regioselective tandem addition reactions of rhenium-bound naphthalene.
J Am Chem Soc.    impact factor:   5.537
2002;  124(13): 3309-15

3:  Murahashi S, Imada Y, Kawakami T, Harada K, Yonemushi Y, Tomita N.
Enantioselective addition of ketene silyl acetals to nitrones catalyzed by chiral titanium complexes. Synthesis of optically active beta-amino acids.
J Am Chem Soc.    impact factor:   5.537
2002;  124(12): 2888-9

4:  Kim S, Lim CJ, Song C, Chung WJ.
Novel radical alkylation of carboxylic imides.
J Am Chem Soc.    impact factor:   5.537
2002;  124(48): 14306-7

5:  Powell SA, Tenenbaum JM, Woerpel KA.
Utilization of 1-oxa-2,2-(dimesityl)silacyclopentane acetals in the stereoselective synthesis of polyols.
J Am Chem Soc.    impact factor:   5.537
2002;  124(43): 12648-9

6Compound ID:21

C2H5NO    59.07

1:  Kleymann G, Fischer R, Betz UA, Hendrix M, Bender W, Schneider U, Handke G, Eckenberg P, Hewlett G, Pevzner V, Baumeister J, Weber O, Henninger K, Keldenich J, Jensen A, Kolb J, Bach U, Popp A, Maben J, Frappa I, Haebich D, Lockhoff O, Rubsamen-Waigmann H.
New helicase-primase inhibitors as drug candidates for the treatment of herpes simplex disease.
Nat Med.    impact factor:   26.584
2002;  8(4): 392-8

2:  Chavez JC, LaManna JC.
Activation of hypoxia-inducible factor-1 in the rat cerebral cortex after transient global ischemia: potential role of insulin-like growth factor-1.
J Neurosci.    impact factor:   8.955
2002;  22(20): 8922-31

3:  Schroder D, Loos J, Thissen R, Dutuit O, Mourgues P, Audier HE, Lifshitz C, Schwarz H.
Barrier height titration by tunable photoionization combined with chemical monitoring: unimolecular keto/enol tautomerization of the acetamide cation radical.
Angew Chem Int Ed Engl.    impact factor:   7.996
2002;  41(15): 2748-51

4:  Rappert A, Biber K, Nolte C, Lipp M, Schubel A, Lu B, Gerard NP, Gerard C, Boddeke HW, Kettenmann H.
Secondary lymphoid tissue chemokine (CCL21) activates CXCR3 to trigger a Cl- current and chemotaxis in murine microglia.
J Immunol.    impact factor:   7.145
2002;  168(7): 3221-6

5:  Richard JP, Williams G, O'Donoghue AC, Amyes TL.
Formation and stability of enolates of acetamide and acetate anion: an Eigen plot for proton transfer at alpha-carbonyl carbon.
J Am Chem Soc.    impact factor:   5.537
2002;  124(12): 2957-68

7Compound ID:23

C4H8O2    88.11

1:  Aevarsson A, Seger K, Turley S, Sokatch JR, Hol WG.
Crystal structure of 2-oxoisovalerate and dehydrogenase and the architecture of 2-oxo acid dehydrogenase multienzyme complexes.
Nat Struct Biol.    impact factor:   13.555
1999;  6(8): 785-92

2:  Nakagawa J, Ishikura S, Asami J, Isaji T, Usami N, Hara A, Sakurai T, Tsuritani K, Oda K, Takahashi M, Yoshimoto M, Otsuka N, Kitamura K.
Molecular characterization of mammalian dicarbonyl/L-xylulose reductase and its localization in kidney.
J Biol Chem.    impact factor:   7.666
2002;  277(20): 17883-91

3:  Gonzalez E, Fernandez MR, Larroy C, Sola L, Pericas MA, Pares X, Biosca JA.
Characterization of a (2R,3R)-2,3-butanediol dehydrogenase as the Saccharomyces cerevisiae YAL060W gene product. Disruption and induction of the gene.
J Biol Chem.    impact factor:   7.666
2000;  275(46): 35876-85

4:  Maestri O, Joset F.
Regulation by external pH and stationary growth phase of the acetolactate synthase from Synechocystis PCC6803.
Mol Microbiol.    impact factor:   6.361
2000;  37(4): 828-38

5:  Sergienko EA, Jordan F.
New model for activation of yeast pyruvate decarboxylase by substrate consistent with the alternating sites mechanism: demonstration of the existence of two active forms of the enzyme.
Biochemistry.    impact factor:   4.493
2002;  41(12): 3952-67

8Compound ID:24

C9H10O3    166.18

1:  Beukelman CJ, Van den Berg AJ, Kroes BH, Labadie RP, Mattsson EE, Van Dijk H.
Plant-derived metabolites with synergistic antioxidant activity.
Immunol Today.    impact factor:   17.134
1995;  16(2): 108

2:  Satriano J, Schlondorff D.
Activation and attenuation of transcription factor NF-kB in mouse glomerular mesangial cells in response to tumor necrosis factor-alpha, immunoglobulin G, and adenosine 3':5'-cyclic monophosphate. Evidence for involvement of reactive oxygen species.
J Clin Invest.    impact factor:   10.921
1994;  94(4): 1629-36

3:  Venugopal SK, Devaraj S, Yang T, Jialal I.
Alpha-tocopherol decreases superoxide anion release in human monocytes under hyperglycemic conditions via inhibition of protein kinase C-alpha.
Diabetes.    impact factor:   9.019
2002;  51(10): 3049-54

4:  Oeckler RA, Kaminski PM, Wolin MS.
Stretch Enhances Contraction of Bovine Coronary Arteries via an NAD(P)H Oxidase-Mediated Activation of the Extracellular Signal-Regulated Kinase Mitogen-Activated Protein Kinase Cascade.
Circ Res.    impact factor:   8.281
2003;  92(1): 23-31

5:  Touyz RM, Chen X, Tabet F, Yao G, He G, Quinn MT, Pagano PJ, Schiffrin EL.
Expression of a functionally active gp91phox-containing neutrophil-type NAD(P)H oxidase in smooth muscle cells from human resistance arteries: regulation by angiotensin II.
Circ Res.    impact factor:   8.281
2002;  90(11): 1205-13

9Compound ID:26

C12H18O3    210.27

no reference available. 
10Compound ID:44

C12H20O2    196.29

no reference available. 

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