Compounds found: 9366
ID Name Structure References (top 10) Molecular Target(s)
21Compound ID:    21
ACETAMIDE

NSC#:25945
NSC#:244792
Aldrich#:00160
Aldrich#:122637
Aldrich#:150703
Aldrich#:487775
Aldrich#:A0500
Properties
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

AKT
ARG
C-AMP
CB-1
ESP
ERK
EGFR-1
EGFR-2
FER
FGFR-1
FLK-1
HGF
KDR
KIT
LC
MER
MET
MUSK
NADPH CYTOCHROME P450
P38
P21
P450
PEST
ROS
SAP
STEP
SRC
TEC
TGF-ALPHA
THIOREDOXIN
THIOREDOXIN REDUCTASE
THYMIDINE KINASE
THYMIDYLATE SYNTHASE
THYMIDYLATE SYNTHETASE
TOPOISOMERASE II ALPHA
PKC
 
22Compound ID:    22
ACETIC ESTER OF L-BETA-ARTEMISIA ALCOHOL

Properties
C12H20O2    196.29



no reference available. 
23Compound ID:    23
ACETOIN

NSC#:7609
NSC#:89727
Aldrich#:00540
Aldrich#:A17951
Properties
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

ARG
CB-1
LC
STEP
 
24Compound ID:    24
APOCYNIN

NSC#:2146
NSC#:209524
Aldrich#:55539
Aldrich#:A10809

Frequency
in 2 ingredients:

  • 257
  • 430
  • in 4 recipes:

  • 26
  • 164
  • 245
  • 463

  • Properties
    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

    ARG
    BCL-2
    C-AMP
    HGF
    JNK
    MET
    P450
    ROS
    STEP
    SRC
    PKC
     
    25Compound ID:    25
    3BETA-ACETOXY-ATRACTYLON

    Frequency
    in 2 ingredients:

  • 92
  • 131
  • in 50 recipes:

  • 20
  • 21
  • 22
  • 27
  • 30
  • 49
  • 69
  • 79
  • 80
  • 96
  • 107
  • 110
  • 156
  • 161
  • 169
  • 173
  • 174
  • 199
  • 219
  • 227
  • 233
  • 241
  • 252
  • 272
  • 280
  • 291
  • 292
  • 301
  • 308
  • 309
  • 319
  • 340
  • 342
  • 346
  • 361
  • 363
  • 376
  • 381
  • 403
  • 437
  • 441
  • 446
  • 449
  • 456
  • 459
  • 469
  • 470
  • 488
  • 490
  • 520

  • Properties
    C17H22O3    274.36



    no reference available. 
    26Compound ID:    26
    D-8-ACETOXYCARVOTANACETO-NE

    Aldrich#:R279137

    Frequency
    in 1 ingredients:

  • 501
  • in 6 recipes:

  • 67
  • 181
  • 292
  • 317
  • 324
  • 472

  • Properties
    C12H18O3    210.27



    no reference available. 
    27Compound ID:    27
    1'-ACETOXYCHAVICOL ACETATE

    Frequency
    in 1 ingredients:

  • 931

  • Properties
    C13H14O4    234.25



    1:  Nakamura Y, Murakami A, Ohto Y, Torikai K, Tanaka T, Ohigashi H.
    Suppression of tumor promoter-induced oxidative stress and inflammatory responses in mouse skin by a superoxide generation inhibitor 1'-acetoxychavicol acetate.
    Cancer Res.    impact factor:   8.614
    1998;  58(21): 4832-9

    2:  Moffatt J, Hashimoto M, Kojima A, Kennedy DO, Murakami A, Koshimizu K, Ohigashi H, Matsui-Yuasa I.
    Apoptosis induced by 1'-acetoxychavicol acetate in Ehrlich ascites tumor cells is associated with modulation of polyamine metabolism and caspase-3 activation.
    Carcinogenesis.    impact factor:   4.118
    2000;  21(12): 2151-7

    3:  Kobayashi Y, Nakae D, Akai H, Kishida H, Okajima E, Kitayama W, Denda A, Tsujiuchi T, Murakami A, Koshimizu K, Ohigashi H, Konishi Y.
    Prevention by 1'-acetoxychavicol acetate of the induction but not growth of putative preneoplastic, glutathione S-transferase placental form-positive, focal lesions in the livers of rats fed a choline-deficient, L-amino acid-defined diet.
    Carcinogenesis.    impact factor:   4.118
    1998;  19(10): 1809-14

    4:  Ohata T, Fukuda K, Murakami A, Ohigashi H, Sugimura T, Wakabayashi K.
    Inhibition by 1'-acetoxychavicol acetate of lipopolysaccharide- and interferon-gamma-induced nitric oxide production through suppression of inducible nitric oxide synthase gene expression in RAW264 cells.
    Carcinogenesis.    impact factor:   4.118
    1998;  19(6): 1007-12

    5:  Tanaka T, Makita H, Kawamori T, Kawabata K, Mori H, Murakami A, Satoh K, Hara A, Ohigashi H, Koshimizu K.
    A xanthine oxidase inhibitor 1'-acetoxychavicol acetate inhibits azoxymethane-induced colonic aberrant crypt foci in rats.
    Carcinogenesis.    impact factor:   4.118
    1997;  18(5): 1113-8

    DT diaphorase
    ROS
     
    28Compound ID:    28
    1'-ACETOXYEUGENOL ACETATE

    Frequency
    in 1 ingredients:

  • 931

  • Properties
    C14H16O5    264.28



    1:  Yu JG.
    [Identification of the chemical components of two Alpinia species]
    Zhong Yao Tong Bao.    impact factor:   0
    1988;  13(6): 34-6, 63

     
    29Compound ID:    29
    9-ACETOXYFUKINANOLIDE

    Frequency
    in 1 ingredients:

  • 932

  • Properties
    C17H24O4    292.37



    1:  Brocksom TJ, Coelho F, Depres JP, Greene AE, Freire De Lima ME, Hamelin O, Hartmann B, Kanazawa AM, Wang Y.
    First Comprehensive Bakkane Approach: Stereoselective and Efficient Dichloroketene-Based Total Syntheses of (+/-)- and (-)-9-Acetoxyfukinanolide, (+/-)- and (+)-Bakkenolide A, (-)-Bakkenolides III, B, C, H, L, V, and X, (+/-)- and (-)-Homogynolide A, (+/-)-Homogynolide B, and (+/-)-Palmosalide C.
    J Am Chem Soc.    impact factor:   5.537
    2002;  124(51): 15313-25

    ABL
    ACK-2
    ALK
    AKT
    ARG
    AXL
    BAS
    BDP-1
    BMX
    BRK
    BTK
    BAD
    BAX
    BCL-2
    BCL-XL
    BLK
    C-AMP
    CB-1
    CCK-4
    CD-45
    CSF-1R
    CSK
    CTK
    c-Met
    DDR
    DEP1
    DT diaphorase
    ESP
    ERK
    ELK
    EphA1
    EphA2
    EphA3
    EphA4
    EphA5
    EphA7
    EphA8
    EphB2
    EphB3
    EphB4
    EphB5
    EGFR-1
    EGFR-2
    EGFR-3
    EGFR-4
    FAK
    FAS
    FAP-1
    FER
    FES
    FGF-2
    FGFR-1
    FGFR-2
    FGFR-3
    FGFR-4
    FLK-1
    FLK-2
    FRK
    FGR
    FYN
    GLEPP-1
    GADD-34
    GADD-45
    GFAP
    GPCR
    GLYOXYLASE I
    GSK-3
    HA-2
    HSC
    HCK
    HGF
    HSP-25
    HMGIC
    IA-2
    IAR
    IGF-1R
    INSR
    IRR
    ITK
    JAK-1
    JAK-2
    JNK
    KDR
    KIT
    LAR
    LC
    LRP
    LTK
    LCK
    LYN
    MMAC-1
    MDM-2
    MEG
    MER
    MET
    MGMT
    MRP
    MUSK
    MDR1
    MEG2
    MLK-3
    MRP
    NADPH CYTOCHROME P450
    NEUROFILAMENT 70
    NM-23
    NAIP
    P38
    P21
    P53
    P450
    PAR-2
    PCP-2
    PDGFR-A
    PDGFR-B
    PEST
    PEZ
    PTEN
    PI-3K
    PTP-1B
    PTP-36
    PTP-S31
    PTP-SL
    PTP-A
    PTP-C
    PTP-D
    PTP-E
    PTP-F
    PTP-G
    PTP-K
    PTP-M
    PTP-S
    PTP-Z
    PTP-20
    PRK
    PYK-2
    PLAG-1
    RET
    RON
    ROR-1
    ROR-2
    Rho GTPase
    Rho Kinase
    ROS
    RYK
    S-100
    SAP
    SHP-1
    SHP-2
    STEP
    SYK
    SRC
    SURVIVIN
    TC-PTP
    TEC
    TEK
    TGF-ALPHA
    TIE
    TNK-1
    TRKA
    TRK-B
    TRK-C
    TXK
    TYK-2
    TYRO-10
    THIOREDOXIN
    THIOREDOXIN REDUCTASE
    THYMIDINE KINASE
    THYMIDYLATE SYNTHASE
    THYMIDYLATE SYNTHETASE
    TOPOISOMERASE II BETA
    TOPOISOMERASE II ALPHA
    TYPE I ACIDIC KERATINS
    TYPE II BASIC KERATINS
    US28
    WAF-1
    WNT-1
    XIAP
    YES
    CIAP1
    CIAP2
    PKC
    hMLH-1
    hMLH-2
    IL-13
    Kirsten-RAS
     
    30Compound ID:    30
    16-ACETOXY-7ALPHA-METHOXYROYLEANONE

    Frequency
    in 1 ingredients:

  • 349

  • Properties
    C23H32O6    404.5



    no reference available. 

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