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Home >> Signaling Pathways >> Ox Stress Reagents

Ox Stress Reagents

Products for  Ox Stress Reagents

  1. Cat.No. Product Name Information
  2. GC19941 DL-Leucic Acid DL-Leucic Acid Chemical Structure
  3. GC11123 α-CEHC

    γTocopherol Metabolite, GTM, 2,7,8trimethyl2(βCarboxyEthyl)6Hydroxychroman

     A major metabolite of δ-tocopherol α-CEHC Chemical Structure
  4. GC52253 α-Enolase (1-19)-biotin Peptide

    Enolase-1 (1-19)-biotin

     A biotinylated α-enolase peptide α-Enolase (1-19)-biotin Peptide Chemical Structure
  5. GC45601 α-Linolenic Acid ethyl ester-d5

    ALAEE-d5, Ethyl α-Linolenate-d5, Ethyl Linolenate-d5, LAEE-d5, Linolenic Acid ethyl ester-d5

       α-Linolenic Acid ethyl ester-d5 Chemical Structure
  6. GC45226 β-BHC

    β-HCH, β-Hexachlorocyclohexane, β-Lindane

     β-BHC is an isomer of the organochlorine pesticide γ-lindane that is a potential impurity found in commercial preparations of lindane. β-BHC Chemical Structure
  7. GC41502 β-Myrcene

    NSC 406264

     β-Myrcene is a terpene that has been found in Cannabis and has antioxidative properties. β-Myrcene Chemical Structure
  8. GC41596 δ-CEHC

    γTocopherol Metabolite, GTM, 2,7,8trimethyl2(βCarboxyEthyl)6Hydroxychroman

     Molecules having vitamin E antioxidant activity include four tocopherols (α, β, γ, δ) and four tocotrienols (α, β, γ, δ). δ-CEHC Chemical Structure
  9. GC48317 δ7-Avenasterol A phytosterol that has antioxidant activities δ7-Avenasterol Chemical Structure
  10. GC41262 (±)-α-CMBHC Vitamin E is a well known antioxidant that exists in eight natural forms: four tocopherols (α, β, δ, and γ) and four tocotrienols (α, β, δ, and γ). (±)-α-CMBHC Chemical Structure
  11. GC41617 (±)-α-Tocopherol

    all-rac-α-Tocopherol, DL-α-Tocopherol

     (±)-α-Tocopherol is a synthetic vitamin E, with antioxidation effect. (±)-α-Tocopherol Chemical Structure
  12. GC45713 (±)-α-Tocopherol Acetate

    all-rac-α-Tocopherol Acetate, DL-α-Tocopherol Acetate, DL-Vitamin E acetate

     (±)-α-Tocopherol Acetate ((±)-Vitamin E acetate), is a orally active synthetic form of vitamin E. (±)-α-Tocopherol Acetate Chemical Structure
  13. GC46313 (±)-α-Tocopherol Acetate-d3

    all-rac-α-Tocopherol Acetate-d3, DL-α-Tocopherol Acetate-d3, DL-Vitamin E Acetate-d3

     A neuropeptide with diverse biological activities (±)-α-Tocopherol Acetate-d3 Chemical Structure
  14. GC40015 (±)-5,7-Dimethyltocol

    rac-5,7-Dimethyltocol, ζ-Tocopherol

     (±)-5,7-Dimethyltocol is a form of tocopherol. (±)-5,7-Dimethyltocol Chemical Structure
  15. GC41213 (±)10-HDHA

    10hydroxy Docosahexaenoic Acid, (±)10HDoHE

    (±)10-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro.

     (±)10-HDHA Chemical Structure
  16. GC41214 (±)11-HDHA

    11hydroxy Docosahexaenoic Acid, (±)11-HDoHE

     (±)11-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)11-HDHA Chemical Structure
  17. GC40428 (±)11-HEDE

    11-hydroxy-12,14-Eicosadienoic Acid

     (±)11-HEDE is produced by non-enzymatic oxidation of 11,14-eicosadienoic acid. (±)11-HEDE Chemical Structure
  18. GC40467 (±)11-HETE

    (±)11-Hydroxyeicosatetraenoic Acid

     (±)11-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. (±)11-HETE Chemical Structure
  19. GC40359 (±)12-HEPE

    (±)12-HEPE is produced by non-enzymatic oxidation of EPA.

     (±)12-HEPE Chemical Structure
  20. GC40429 (±)12-HETE

    (±)-Hydroxyeicosatetraenoic Acid

    (±)12-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid.

     (±)12-HETE Chemical Structure
  21. GC48738 (±)12-HETE-d8

    (±)12-Hydroxyeicosatetraenoic Acid-d8

     (±)12-HETE-d8 Chemical Structure
  22. GC41192 (±)13-HDHA

    13hydroxy Docosahexaenoic Acid, (±)13-HDoHE

     (±)13-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)13-HDHA Chemical Structure
  23. GC41649 (±)13-HODE cholesteryl ester (±)13-HODE cholesteryl ester was originally extracted from atherosclerotic lesions and shown to be produced by Cu2+-catalyzed oxidation of LDL. (±)13-HODE cholesteryl ester Chemical Structure
  24. GC40355 (±)13-HpODE

    13-Hydroperoxylinoleic acid; Linoleic acid 13-hydroperoxide

    (±)13-HpODE is a racemic mixture of hydroperoxides derived non-enzymatically from linoleic acid through the action of reactive oxygen species.

     (±)13-HpODE Chemical Structure
  25. GC41193 (±)14-HDHA

    14hydroxy Docosahexaenoic Acid, (±)14-HDoHE

     (±)14-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)14-HDHA Chemical Structure
  26. GC40420 (±)15-HEDE (±)15-HEDE is produced by non-enzymatic oxidation of 11,14-eicosadienoic acid. (±)15-HEDE Chemical Structure
  27. GC40361 (±)15-HEPE

    (±)15-hydroxy Eicosapentaenoic Acid

    (±)15-HEPE is produced by non-enzymatic oxidation of EPA.

     (±)15-HEPE Chemical Structure
  28. GC40433 (±)15-HETE MaxSpec® Standard (±)15-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. (±)15-HETE MaxSpec® Standard Chemical Structure
  29. GC48739 (±)15-HETE-d8

    (±)15-Hydroxyeicosatetraenoic Acid-d8

     (±)15-HETE-d8 Chemical Structure
  30. GC41196 (±)16-HDHA

    16hydroxy Docosahexaenoic Acid, (±)16-HDoHE

     (±)16-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)16-HDHA Chemical Structure
  31. GC41197 (±)17-HDHA

    17-hydroxy Docosahexaenoic Acid, 17-hydroxy DHA, (±)17-HDoHE

     (±)17-HDHA is an autoxidation product of docosahexaenoic acid in vitro. (±)17-HDHA Chemical Structure
  32. GC41198 (±)17-HDHA MaxSpec® Standard

    17-hydroxy Docosahexaenoic Acid, 17-hydroxy DHA, (±)17-HDoHE

     (±)17-HDHA is an autoxidation product of docosahexaenoic acid in vitro. (±)17-HDHA MaxSpec® Standard Chemical Structure
  33. GC40362 (±)18-HEPE (±)18-HEPE is produced by non-enzymatic oxidation of EPA. (±)18-HEPE Chemical Structure
  34. GC41202 (±)4-HDHA

    4hydroxy Docosahexaenoic Acid, (±)4HDoHE

     (±)4-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)4-HDHA Chemical Structure
  35. GC40364 (±)5-HEPE (±)5-HEPE is produced by non-enzymatic oxidation of EPA. (±)5-HEPE Chemical Structure
  36. GC40439 (±)5-HETE

    (±)5-Hydroxyeicosatetraenoic Acid

    (±)5-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid.

     (±)5-HETE Chemical Structure
  37. GC40828 (±)5-HETE lactone

    (±)5-Hydroxyeicosatetraenoic Acid lactone

     (±)5-HETE lactone is a cyclic ester formed by acid-catalyzed nucleophilic addition of the C-5 hydroxyl to the C-1 carboxyl of (±)5-HETE. (±)5-HETE lactone Chemical Structure
  38. GC40837 (±)5-HETE methyl ester

    (±)-Hydroxyeicosatetraenoic Acid methyl ester

     (±)5-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. (±)5-HETE methyl ester Chemical Structure
  39. GC40576 (±)5-iPF2α-VI

    iPF2αI, Isoprostane F2α-I, 5-iso PGF2α-VI, 5-iso Prostaglandin F2α-VI

     Isoprostanes are prostaglandin (PG)-like products of free-radical induced lipid peroxidation. (±)5-iPF2α-VI Chemical Structure
  40. GC46263 (±)5-iPF2α-VI-d11 An internal standard for the quantification of (±)5iPF2αVI (±)5-iPF2α-VI-d11 Chemical Structure
  41. GC41204 (±)7-HDHA

    7hydroxy Docosahexaenoic Acid, (±)7HDoHE

    (±)7-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro.

     (±)7-HDHA Chemical Structure
  42. GC41205 (±)8-HDHA

    8hydroxy Docosahexaenoic Acid, (±)8HDoHE

     (±)8-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)8-HDHA Chemical Structure
  43. GC40366 (±)8-HEPE

    (±)8-HEPE is produced by non-enzymatic oxidation of EPA.

     (±)8-HEPE Chemical Structure
  44. GC40367 (±)9-HEPE (±)9-HEPE is produced by non-enzymatic oxidation of EPA. (±)9-HEPE Chemical Structure
  45. GC40443 (±)9-HETE

    (±)9-Hydroxyeicosatetraenoic Acid

     (±)9-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. (±)9-HETE Chemical Structure
  46. GC40541 (±)9-HODE

    (±)9-HODE is one of the two racemic monohydroxy fatty acids resulting from the non-enzymatic oxidation of linoleic acid.

     (±)9-HODE Chemical Structure
  47. GC40356 (±)9-HpODE (±)9-HpODE is a racemic mixture of the fatty acid hydroperoxide product (9(S)-HpODE) formed from lipoxygenase action on linoleic acid. (±)9-HpODE Chemical Structure
  48. GC40218 (-)-Epigallocatechin Gallate-d3/d4

    EGCG-d3/d4

     (-)-Epigallocatechin gallate-d3/d4 is intended for use as an internal standard for the quantification of (-)-epigallocatechin gallate by GC- or LC-MS. (-)-Epigallocatechin Gallate-d3/d4 Chemical Structure
  49. GC45248 (-)-FINO2 (-)-FINO2 is a ferroptosis-inducing peroxide compound that indirectly inhibits glutathione peroxidase 4 (GPX4) and oxidizes iron. (-)-FINO2 Chemical Structure
  50. GC90533 (-)-Pinoresinol

    A lignan with diverse biological activities

     (-)-Pinoresinol Chemical Structure
  51. GC49690 (3R,5R)-Rosuvastatin (calcium salt) A potential impurity found in bulk preparations of rosuvastatin (3R,5R)-Rosuvastatin (calcium salt) Chemical Structure
  52. GC41700 (E)-2-(2-Chlorostyryl)-3,5,6-trimethylpyrazine

    CSTMP

     (E)-2-(2-Chlorostyryl)-3,5,6-trimethylpyrazine (CSTMP) is a stilbene derivative with antioxidant and anticancer activities. (E)-2-(2-Chlorostyryl)-3,5,6-trimethylpyrazine Chemical Structure
  53. GC49003 (E)-Ajoene

    NSC 614554

     A disulfide with diverse biological activities (E)-Ajoene Chemical Structure
  54. GC26181 (±)-Catechin

    rel-Cianidanol; rel-Catechuic acid

    (±) - Catechin (rel Xianidanol) is the racemate of Catechin.

     (±)-Catechin Chemical Structure
  55. GC19824 (±)-Pinocembrin

    (+)-Pinocembrin, Dihydrochrysin, NSC 279005

     (±)-Pinocembrin ((±)-5,7-Dihydroxyflavanone) is a GPR120 ligand able to promote wound healing in HaCaT cell line. (±)-Pinocembrin Chemical Structure
  56. GC19461 (±)13-HODE

    (±)13-HODE is one of the two racemic monohydroxy fatty acids resulting from the non-enzymatic oxidation of linoleic acid.

     (±)13-HODE Chemical Structure
  57. GC49034 1(R)-(Trifluoromethyl)oleyl alcohol An oleic acid analog 1(R)-(Trifluoromethyl)oleyl alcohol Chemical Structure
  58. GC41837 1,3,7-Trimethyluric Acid

    8-oxo Caffeine, NSC 11259

    1,3,7-Trimethyluric acid is a methyl derivative of uric acid and a product of C-8 oxidation of caffeine by cytochrome P450 enzymes.

     1,3,7-Trimethyluric Acid Chemical Structure
  59. GC46387 1,3,7-Trimethyluric Acid-d9

    TMU-d9, 8-oxo Caffeine-d9

     An internal standard for the quantification of 1,3,7-trimethyluric acid 1,3,7-Trimethyluric Acid-d9 Chemical Structure
  60. GC46481 1-Hydroxyphenazine

    Hemipyocyanine, NSC 88882

     A P. aeruginosa virulence factor 1-Hydroxyphenazine Chemical Structure
  61. GC18235 1-O-Hexadecyl-sn-glycerol

    α-Chimyl Alcohol, (S)-(+)-Chimyl Alcohol

    1-O-Hexadecyl-sn-glycerol is a bioactive alkyl glyceryl ether.

     1-O-Hexadecyl-sn-glycerol Chemical Structure
  62. GC40146 1-Oleoyl-2-Palmitoyl-rac-glycerol

    18:1/16:0-DG, DG(18:1/16:0/0:0), 1,2-OP, 1-Olein-2-Palmitin

     1-Oleoyl-2-palmitoyl-rac-glycerol (1,2-OP) is a diacylglycerol containing oleic acid at the sn-1 position and palmitic acid at the sn-2 position. 1-Oleoyl-2-Palmitoyl-rac-glycerol Chemical Structure
  63. GC42026 1-Palmitoyl-2-hydroxy-sn-glycero-3-PC

    1-Hexadecanoyl-sn-glycero-3-Phosphatidylcholine, 1-Hexadecanoyl-sn-glycero-3-Phosphocholine, 1-Hexadecanoyl-sn-glycerol-3-Phosphorylcholine, Lyso-PC, 1-Palmitoyl-sn-glycero-3-Phosphocholine, PC(16:0/0:0), 16:0/0:0-PC

     1-Palmitoyl-2-hydroxy-sn-glycero-3-PC is an abundant gonadal LPC (lysophosphatidylcholine). 1-Palmitoyl-2-hydroxy-sn-glycero-3-PC Chemical Structure
  64. GC46490 1-Palmitoyl-d3-2-hydroxy-sn-glycero-3-PC

    1-Hexadecanoyl-sn-glycero-3-Phosphatidylcholine-d3, 1-Hexadecanoyl-sn-glycero-3-Phosphocholine-d3, LPC-d3, 16:0/0:0(d3) Lyso-PC, 1-Palmitoyl-sn-glycero-3-Phosphocholine-d3, PC(16:0/0:0)-d3, 16:0/0:0-PC-d3

     A neuropeptide with diverse biological activities 1-Palmitoyl-d3-2-hydroxy-sn-glycero-3-PC Chemical Structure
  65. GC45693 1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PC

    1-Hexadecanoyl-d9-sn-glycero-3-Phosphatidylcholine, 1-Hexadecanoyl-d9-sn-glycero-3-Phosphocholine, 16:0(d9) Lyso-PC, PC(16:0-d9/0:0), 16:0-d9/0:0-PC

     A quantitative analytical standard guaranteed to meet MaxSpec® identity, purity, stability, and concentration specifications 1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PC Chemical Structure
  66. GC48782 10,13-epoxy-11-methyl-Octadecadienoic Acid

    F2 Furan Fatty Acid, 3-methyl-5-pentyl-2-Furannonanoic Acid, 9M5

     A furan fatty acid 10,13-epoxy-11-methyl-Octadecadienoic Acid Chemical Structure
  67. GC41866 10-methyl-9-(phenoxycarbonyl) Acridinium (trifluoromethylsulfonate) 10-methyl-9-(phenoxycarbonyl) Acridinium is an acridinium ester that produces fluorescent 10-methyl-9-acridone upon oxidation with hydrogen peroxide, persulfates, and other oxidants in alkaline conditions. 10-methyl-9-(phenoxycarbonyl) Acridinium (trifluoromethylsulfonate) Chemical Structure
  68. GC41868 10-Nitrooleate

    10Nitrooleic Acid, 10nitro9transOctadecenoic Acid

     10-Nitrooleate (CXA-10), a nitro fatty acid, has potential effects in disease states in which oxidative stress, inflammation, fibrosis, and/or direct tissue toxicity play significant roles. 10-Nitrooleate Chemical Structure
  69. GC41893 13(R)-HODE cholesteryl ester 13(R)-HODE cholesteryl ester was originally extracted from atherosclerotic lesions. 13(R)-HODE cholesteryl ester Chemical Structure
  70. GC46442 15(S)-HETE-d8

    15(S)-Hydroxyeicosatetraenoic Acid-d8

     An internal standard for the quantification of 15-HETE 15(S)-HETE-d8 Chemical Structure
  71. GC46452 16-Oxokahweol A synthetic diterpene 16-Oxokahweol Chemical Structure
  72. GC40947 2,3-Dimethoxy-5-methyl-p-benzoquinone

    Coenzyme Q0, CoQ0

     2,3-Dimethoxy-5-methyl-p-benzoquinone (CoQ0) is a potent, oral active ubiquinone compound can be derived from Antrodia cinnamomea. 2,3-Dimethoxy-5-methyl-p-benzoquinone Chemical Structure
  73. GC90081 2,3-dinor-8-iso Prostaglandin F1α

    An active metabolite of arachidonic acid and 8-iso PGF2α

     2,3-dinor-8-iso Prostaglandin F1α Chemical Structure
  74. GC40416 2,3-dinor-8-iso Prostaglandin F2α

    2,3-dinor-iPF2α-III, 2,3-dinor-8-iso PGF2α

     8-iso Prostaglandin F2α (8-iso PGF2α; 8-isoprostane) is a prostaglandin-like product of non-specific lipid peroxidation. 2,3-dinor-8-iso Prostaglandin F2α Chemical Structure
  75. GC46057 2,5-Dihydroxycinnamic Acid phenethyl ester An inhibitor of 5-LO 2,5-Dihydroxycinnamic Acid phenethyl ester Chemical Structure
  76. GC40503 2-HOBA

    2-(Aminomethyl)phenol, 2-Hydroxybenzylamine, NSC 127870

     2-HOBA (2-HOBA) a selective dicarbonyl scavenger, is an antioxidant and scavanger of free radicals and isolevuglandins (IsoLGs). 2-HOBA Chemical Structure
  77. GC49172 2-hydroxy Estrone

    Catecholestrone, 2-hydroxy E1, 2-OHE1

     An active metabolite of estrone 2-hydroxy Estrone Chemical Structure
  78. GC19768 2-Keto-D-gluconic acid hemicalcium salt monohydrate

    2-keto D-Gluconate, 2-KGA

     2-Keto-D-gluconic acid hemicalcium salt monohydrate Chemical Structure
  79. GC49840 2-Methylbutyrylglycine

    2-MBG, N-sec-Valerylglycine

     A metabolite of isoleucine 2-Methylbutyrylglycine Chemical Structure
  80. GC42195 2-Thiobarbituric Acid

    4,6-dihydroxy-2-mercaptopyrimidine, TBA, Thiobarbituric acid

     2-Thiobarbituric acid is a colorimetric reagent commonly used in the detection of malondialdehyde (MDA), a marker of lipid peroxidation. 2-Thiobarbituric Acid Chemical Structure
  81. GC41210 22-HDHA

    22-hydroxy Docosahexaenoic Acid, 22-OH DHA

     22-HDHA is an oxidation product of docosahexaenoic acid. 22-HDHA Chemical Structure
  82. GC49005 2S-Eriodictyol

    (+)-Eriodictyol

     A flavanone with antioxidant activity 2S-Eriodictyol Chemical Structure
  83. GC40618 3',4',7-Trihydroxyisoflavone

    3'-hydroxy Daidzein, 3’,4’,7-THIF

     3',4',7-Trihydroxyisoflavone, a major metabolite of Daidzein, is an ATP-competitive inhibitor of Cot (Tpl2/MAP3K8) and MKK4. 3',4',7-Trihydroxyisoflavone has anticancer, anti-angiogenic, chemoprotective, and free radical scavenging activities. 3',4',7-Trihydroxyisoflavone Chemical Structure
  84. GC48395 3,3',5-Triiodo-L-thyronine (sodium salt hydrate)

    Liothyronine, T3, L3,3',5Triiodothyronine

     3,3',5-Triiodo-L-thyronine (sodium salt hydrate) is an active form of thyroid hormone. 3,3',5-Triiodo-L-thyronine (sodium salt hydrate) Chemical Structure
  85. GC42203 3,4',5-Trismethoxybenzophenone Resveratrol is a potent phenolic antioxidant found in natural sources that has antiproliferative activity. 3,4',5-Trismethoxybenzophenone Chemical Structure
  86. GC46557 3,4-Dihydroquinolin-2(1H)-one A building block 3,4-Dihydroquinolin-2(1H)-one Chemical Structure
  87. GC46577 3,5-Dihydroxybenzaldehyde

    α-Resorcylaldehyde

     A building block 3,5-Dihydroxybenzaldehyde Chemical Structure
  88. GC18205 3,5-Diiodothyroacetic Acid

    Diac, NSC 90463, T2A, TA2

     3,5-Diiodothyroacetic acid (diac) is the acetic acid variant of thyroxine. 3,5-Diiodothyroacetic Acid Chemical Structure
  89. GC49169 3,8’-Biapigenin

    I3,II8-Biapigenin, 3,8\-Biapigenin

     A biflavonoid with diverse biological activities 3,8’-Biapigenin Chemical Structure
  90. GC52324 3-(3-Hydroxyphenyl)propionic Acid sulfate

    3-HPPA sulfate

     A metabolite of certain phenols and glycosides 3-(3-Hydroxyphenyl)propionic Acid sulfate Chemical Structure
  91. GC49849 3-Aminosalicylic Acid

    3-ASA, NSC 285111

     A salicylic acid derivative 3-Aminosalicylic Acid Chemical Structure
  92. GC42251 3-Bromotyrosine (trifluoroacetate salt)

    3-bromo-Tyr

     3-Bromotyrosine is a product of protein oxidation found after activation of eosinophils during an allergic response. 3-Bromotyrosine (trifluoroacetate salt) Chemical Structure
  93. GC42252 3-Bromotyrosine-13C9,15N (trifluoroacetate salt)

    3-bromo-Tyr-13C9,15N

     3-Bromotyrosine-13C9,15N is intended for use as an internal standard for the quantification of 3-bromotyrosine by GC- or LC-MS. 3-Bromotyrosine-13C9,15N (trifluoroacetate salt) Chemical Structure
  94. GC13377 3-hydroxy Anthranilic Acid

    3-HAA,NSC 522891

     co-antioxidant 3-hydroxy Anthranilic Acid Chemical Structure
  95. GC49364 3-Hydroxycoumarin

    3-Coumarinol, NSC 74691

     A coumarin with diverse biological activities 3-Hydroxycoumarin Chemical Structure
  96. GC45337 3-Hydroxyterphenyllin

    NSC 299113

     3-Hydroxyterphenyllin is a metabolite of Aspergillus candidus.3-Hydroxyterphenyllin suppresses proliferation and causes cytotoxicity against A2780/CP70 and OVCAR-3 cells. 3-Hydroxyterphenyllin induces S phase arrest and apoptosis. 3-Hydroxyterphenyllin has the potential for the research of ovarian cancer. 3-Hydroxyterphenyllin Chemical Structure
  97. GC46609 4-(Phenylcarbonyl)benzoic Acid

    4-Benzoylbenzoic Acid, 4-Carboxybenzophenone, NSC 37115, p-Benzoylbenzoic Acid, p-Carboxybenzophenone

     A photooxidant 4-(Phenylcarbonyl)benzoic Acid Chemical Structure
  98. GC42338 4-Aminobenzoic Acid hydrazide

    4ABAH, Myeloperoxidase Inhibitor 1, NSC 640

     4-Aminobenzoic Acid hydrazide is an irreversible MPO myeloperoxidase inhibitor with an IC50 of 0.3 μM. 4-Aminobenzoic Acid hydrazide Chemical Structure
  99. GC42351 4-carboxy TEMPO

    4-Carboxyl-2,2,6,6-tetramethylpiperidin-1-oxyl

     4-carboxy TEMPO is a nitroxide and spin label. 4-carboxy TEMPO Chemical Structure
  100. GC42400 4-hydroperoxy 2-Nonenal

    4HpNE

     4-hydroxy Nonenal is a lipid peroxidation product derived from oxidized ω-6 polyunsaturated fatty acids, such as linoleic acid and arachidonic acid, that is widely used as a marker of oxidative stress. 4-hydroperoxy 2-Nonenal Chemical Structure
  101. GC18858 4-hydroxy Alternariol

    4-hydroxy AOH, 4-OH AOH

     4-hydroxy Alternariol is a metabolite of the mycotoxin alternariol formed through cytochrome P450 (CYP450) metabolism. 4-hydroxy Alternariol Chemical Structure

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