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Inicio >> Signaling Pathways >> Cancer Biology

Cancer Biology

Products for  Cancer Biology

  1. Cat.No. Nombre del producto Información
  2. GC47361 Fludioxonil

    CGA 173506

     A fungicide Fludioxonil Chemical Structure
  3. GC92113 FNIII14 (sodium salt)

    FNIII14-2

     FNIII14 (sodium salt) es un inhibidor de la adhesión celular y un péptido derivado de la 14 ª repetición de tipo III, que es parte del dominio de Unión a la heparina 2, de humanos, ratones y ratas fibronectina. FNIII14 (sodium salt) Chemical Structure
  4. GC49074 Forphenicine A bacterial metabolite and an inhibitor of alkaline phosphatase Forphenicine Chemical Structure
  5. GC52014 Forphenicinol

    Forfenimex

     An immunomodulator and a derivative of forphenicine Forphenicinol Chemical Structure
  6. GC47372 Foxy-5 (trifluoroacetate salt)

    N-formyl-Met-Asp-Gly-Cys-Glu-Leu, N-formyl-MDGCEL

     A neuropeptide with diverse biological activities Foxy-5 (trifluoroacetate salt) Chemical Structure
  7. GC49089 FR900359

    UBO-QIC

     FR900359 is an inhibitor of G proteins Gαq, Gα11, and Gα14 with IC50 values of 13.18, 10.47, and 10nM, respectively and is isolated from the leaves of the ornamental plant Ardisia crenata FR900359 Chemical Structure
  8. GC16236 Fucoidan

    Fucan,Sulfated α-L-Fucan

     Fucoidan, un polisacÁrido biolÓgicamente activo, es un inhibidor eficaz de la α-amilasa y la α-glucosidasa. Fucoidan Chemical Structure
  9. GC52483 Fucosylated Ganglioside GM1 (porcine) (ammonium salt)

    Fucosylated Monosialoganglioside GM1, Fucosyl GM1

     A sphingolipid Fucosylated Ganglioside GM1 (porcine) (ammonium salt) Chemical Structure
  10. GC47377 Fumitremorgin B

    Lanosulin

     Fumitremorgin B es una micotoxina tremorgénica. Fumitremorgin B Chemical Structure
  11. GC12604 Fumonisin B1

    伏马菌素B1

    La fumonisina B1 es una micotoxina producida por F. moniliforme, un hongo prevalente en el maíz y otros granos.

     Fumonisin B1 Chemical Structure
  12. GC52288 Fumonisin B1-13C34

    FB1-13C34

     An internal standard for the quantification of fumonisin B1 Fumonisin B1-13C34 Chemical Structure
  13. GC47378 Fumonisin B2-13C34

    FB2

     An internal standard for the quantification of fumonisin B2 Fumonisin B2-13C34 Chemical Structure
  14. GC47379 Fumonisin B3-13C34

    FB3-13C34

     A neuropeptide with diverse biological activities Fumonisin B3-13C34 Chemical Structure
  15. GC52047 Fustin

    Dihydrofisetin, NSC 59264

     Fustinis ((±)-Fustin; 3,7,3',4'-Tetrahidroxiflavanona) es un potente inhibidor del amiloide β (Aβ). Fustin Chemical Structure
  16. GP10092 G protein coupled receptor [Homo sapiens]

    H2N-Gln-Glu-Ser-His-Asn-Ser-Gly-Asn-Arg-Ser-Asp-Gly-Pro-Gly-Lys-Asn-Thr-Thr-Leu-His-Asn-Glu-Phe-Asp-Thr-OH

    G protein coupled receptor [Homo sapiens], (C110H168N38O45), a peptide with the sequence H2N-QESHNSGNRSDGPGKNTTLHNEFDT-OH, MW= 2742.74. G protein coupled receptor [Homo sapiens] Chemical Structure
  17. GC49420 Gallic Acid-d2

    3,4,5-Trihydroxybenzoic Acid-d2

     An internal standard for the quantification of gallic acid Gallic Acid-d2 Chemical Structure
  18. GC43727 Ganglioside GD1a mixture (sodium salt)

    Ganglioside B1

    Ganglioside GD1a is a sialic acid-containing glycosphingolipid found in brain, erythrocytes, bone marrow, testis, spleen, and liver.

     Ganglioside GD1a mixture (sodium salt) Chemical Structure
  19. GC43728 Ganglioside GD1b Mixture (sodium salt)

    Disialoganglioside GD1b, Ganglioside C1, Ganglioside G2

     Ganglioside GD1b is an acidic glycosphingolipid that contains two sialic acid residues linked to an inner galactose unit. Ganglioside GD1b Mixture (sodium salt) Chemical Structure
  20. GC49490 Ganglioside GD2 Mixture (bovine buttermilk) (ammonium salt)

    Disialoganglioside GD2 Mixture, Ganglioside GD2, Disialo Mixture

     A semi-synthetic mixture of ganglioside GD2 Ganglioside GD2 Mixture (bovine buttermilk) (ammonium salt) Chemical Structure
  21. GC52505 Ganglioside GT1b (bovine) (sodium salt)

    Ganglioside G1, Trisialoganglioside GT1b

     A sphingolipid Ganglioside GT1b (bovine) (sodium salt) Chemical Structure
  22. GC43735 Ganglioside GT1b Mixture (sodium salt)

    Ganglioside G1 Mixture

    Ganglioside GT1b is a trisialoganglioside that is characterized by having two sialic residues linked to the inner galactose unit.

     Ganglioside GT1b Mixture (sodium salt) Chemical Structure
  23. GC49229 Ganodermanontriol Ganodermanontriol, un esterol aislado de Ganoderma lucidum, induce actividad antiinflamatoria en células hepÁticas daÑadas por hidroperÓxido de terc-butilo (t-BHP) a través de la expresiÓn de HO-1. Ganodermanontriol exhibe actividad hepatoprotectora. Ganodermanontriol Chemical Structure
  24. GP10107 Gap 26

    Val-Cys-Tyr-Asp-Lys-Ser-Phe-Pro-Ile-Ser-His-Val-Arg

    Gap 26, as a connexin mimetic peptide, which has the SHVR amino acid regions contributing crucially to the docking of connexons to generate gap junctions. Gap 26 Chemical Structure
  25. GP10119 Gap 27

    Ser-Arg-Pro-Thr-Glu-Lys-Thr-Ile-Phe-Ile-Ile

    A connexin-mimetic peptide

     Gap 27 Chemical Structure
  26. GC43747 Geranylgeranyl Pyrophosphate (ammonium salt)

    GGPP

    El pirofosfato de geranilgeranilo es un intermediario en la vía de la HMG-CoA reductasa derivado directamente del pirofosfato de farnesilo y utilizado en la biosíntesis de terpenos y terpenoides.

     Geranylgeranyl Pyrophosphate (ammonium salt) Chemical Structure
  27. GC48763 Gestodene-d6

    SHB 331-d6; WL 70-d6

     An internal standard for the quantification of gestodene Gestodene-d6 Chemical Structure
  28. GC18840 Gilvocarcin V

    Anandimycin A, Antibiotic 1072B, DC38V, NSC 338943, NSC 348115, Toromycin A

     Gilvocarcin V is an antitumor antibiotic with a coumarin-based aromatic structure that was orignally isolated from the culture broth of S. Gilvocarcin V Chemical Structure
  29. GC20007 Ginsenoside CK

    Ginsenoside Compound K, Ginsenoside IH901; Compound K

    Ginsenoside C-K, a bacterial metabolite of G-Rb1, exhibits anti-inflammatory effects by reducing iNOS and COX-2. Ginsenoside C-K exhibits an inhibition against the activity of CYP2C9 and CYP2A6 in human liver microsomes with IC50s of 32.0±3.6 μM and 63.6±4.2 μM, respectively.

     Ginsenoside CK Chemical Structure
  30. GC45811 GKK1032B GKK1032B es un compuesto alcaloide que se puede encontrar en el hongo endÓfito Penicillium sp. GKK1032B puede inducir la apoptosis de las células MG63 del osteosarcoma humano a través de la activaciÓn de la vÍa de la caspasa. GKK1032B Chemical Structure
  31. GC40049 Glucocorticoid Resistance Inhibitor Glucocorticoid resistance inhibitor is an inhibitor of glucocorticoid resistance. Glucocorticoid Resistance Inhibitor Chemical Structure
  32. GC92031 GPX4 Inhibitor 17

    Glutathione Peroxidase 4-IN-17; Glutathione Peroxidase 4 Inhibitor 17; GPX4-IN-17

     GPX4 Inhibitor 17 es un inhibidor de la glutatión peroxid4 (GPX4) y un inductor de la ferroptosis. GPX4 Inhibitor 17 Chemical Structure
  33. GC48720 Griseofulvic Acid

    (±)-Griseofulvic Acid

     A metabolite of griseofulvin Griseofulvic Acid Chemical Structure
  34. GC74557 Grisnilimab

    WT1

     Grisnilimab (WT1), un anticuerpo monoclonal IgG2a anti-CD7, es un supresor tumoral implicado en la etiología del tumor de Wilms. Grisnilimab Chemical Structure
  35. GC43784 GRP (human) (trifluoroacetate salt)

    Gastrin-Releasing Peptide (1-27) (human)

     Gastrin-releasing peptide (GRP) is a neuropeptide that stimulates gastrin release. GRP (human) (trifluoroacetate salt) Chemical Structure
  36. GC39491 GSK-3484862 GSK-3484862 es un inhibidor no covalente de la ADN metiltransferasa (Dnmt1). GSK-3484862 induce la hipometilaciÓn del ADN contra el cÁncer. GSK-3484862 media la desmetilaciÓn dramÁtica en células madre embrionarias murinas con una toxicidad no especÍfica mÍnima. GSK-3484862 Chemical Structure
  37. GP10115 GTP-Binding Protein Fragment, G alpha

    H2N-Cys-Gly-Ala-Gly-Glu-Ser-Gly-Lys-Ser-Thr-Ile-Val-Lys-Gln-Met-Lys-OH

    GTP-Binding Protein Fragment, G alpha Chemical Structure
  38. GC49048 Guanylin (human) (trifluoroacetate salt) A peptide hormone activator of GC-C Guanylin (human) (trifluoroacetate salt) Chemical Structure
  39. GC43804 Halofuginone (hydrochloride) Halofuginone is a halogenated derivative of febrifugine, a natural quinazolinone-containing compound found in the Chinese herb D. Halofuginone (hydrochloride) Chemical Structure
  40. GC49855 Harmalol (hydrochloride hydrate)

    11-hydroxy Harmalan, Harmidol

     A β-carboline alkaloid and an active metabolite of harmaline Harmalol (hydrochloride hydrate) Chemical Structure
  41. GC40724 Heat Shock Protein Inhibitor II

    Hsp Inhibitor II, KNK 423

     Heat shock protein (Hsp) inhibitor II is the active form of Hsp inhibitor I and a benzylidene lactam compound that prevents the synthesis of inducible Hsps, such as Hsp105, Hsp72, and Hsp40. Heat Shock Protein Inhibitor II Chemical Structure
  42. GC48388 Heliquinomycin

    NSC 702208, Rubymycin

     A bacterial metabolite with diverse biological activities Heliquinomycin Chemical Structure
  43. GC49882 Hemokinin 1 (human) (trifluoroacetate salt)

    HK-1, TGKASQFFGLM-NH2, Thr-Gly-Lys-Ala-Ser-Gln-Phe-Phe-Gly-Leu-Met-NH2

     A peptide agonist of NK1 receptors Hemokinin 1 (human) (trifluoroacetate salt) Chemical Structure
  44. GC49915 Hexa-D-Arginine (trifluoroacetate salt)

    Furin Inhibitor II, Hexa-D-Arg-NH2, Hexa-D-Arginine amide, D6R-NH2, (D)RRRRRR-NH2

     A furin inhibitor Hexa-D-Arginine (trifluoroacetate salt) Chemical Structure
  45. GP10020 Histone-H2A-(107-122)-Ac-OH

    Ac-Gly-Val-Leu-Pro-Asn-Ile-Gln-Ala-Val-Leu-Leu-Pro-Lys-Lys-Thr-Glu-OH

    Histone-H2A peptide

     Histone-H2A-(107-122)-Ac-OH Chemical Structure
  46. GC43866 Histrelin (acetate)

    Des-Gly10,D-His(Bzl)6-LHRHethyl amide, Des-Gly10,D-His(Bzl)6,Pro-NHEt9-LHRH, (ImBzl)-d-His6,Pro9-NET-LHRH

     Histrelin is a synthetic gonadotropin-releasing hormone (GNRH) agonist that binds to the GNRH receptor (GNRHR; Ki = 0.2 nM in CHO cells expressing the human receptor). Histrelin (acetate) Chemical Structure
  47. GC52504 Human Vitamin D Receptor Reporter Assay System

    NR1I1, VDR

     A nuclear receptor cell-based reporter assay Human Vitamin D Receptor Reporter Assay System Chemical Structure
  48. GC49282 Hydroxy Lenalidomide

    5-hydroxy Lenalidomide

     A metabolite of lenalidomide Hydroxy Lenalidomide Chemical Structure
  49. GC74558 Ianalumab

    VAY-736

     Ianalumab (VAY-736) es un anticuerpo humano descarboxilado contra BAFF-R. Ianalumab Chemical Structure
  50. GC62100 Ibacitabine La ibacitabina, un compuesto antiviral, se puede utilizar para la secuenciaciÓn de genes. Ibacitabine Chemical Structure
  51. GC45959 IKD-8344 A macrocyclic dilactone with diverse biological activities IKD-8344 Chemical Structure
  52. GC49359 IM-156 (acetate)

    HL156A, HL271

     A mitochondrial complex I inhibitor and an AMPKα activator IM-156 (acetate) Chemical Structure
  53. GC52190 Imidazole Ketone Erastin

    IKE

     Imidazole Ketone Erastin is an effective and metabolically stable system xc- inhibitor and ferroptosis inducer. Imidazole Ketone Erastin Chemical Structure
  54. GC47454 IMS 2186 An anti-choroidal neovascularization agent IMS 2186 Chemical Structure
  55. GC52472 Inostamycin A (sodium salt)

    Inostamycin

     A bacterial metabolite with anticancer activity Inostamycin A (sodium salt) Chemical Structure
  56. GP10041 Insulin like growth factor II fragment variant

    H2N-Thr-Pro-Thr-Lys-Ser-Glu-Arg-OH

    Insulin like growth factor II fragment variant has a sequence of Thr-Pro-Thr-Lys-Ser-Glu-Arg. Insulin like growth factor II fragment variant Chemical Structure
  57. GC48396 IR 780 IR 780 is a heptacyanine fluorescent probe for in vivo imaging of tumor cells with a large absorption spectrum of 750-830nm. IR 780 Chemical Structure
  58. GC48378 IR 783 A fluorescent probe for in vivo tumor cell imaging IR 783 Chemical Structure
  59. GC49634 Isoflupredone

    Δ-Fluorocortisone, 9α-Fluoroprednisolone, NSC 12174

     La isoflupredona pertenece a la clase de los corticosteroides y ejerce su efecto uniéndose a los receptores de glucocorticoides y mineralocorticoides de animales, como los caballos. Isoflupredone Chemical Structure
  60. GC43920 Isoquinoline-3-carboxylic Acid

    3-Carboxyisoquinoline, 3-Isoquinaldic Acid, NSC 53385

     Isoquinoline-3-carboxylic acid is a synthetic intermediate that has been used to design novel antitumor compounds. Isoquinoline-3-carboxylic Acid Chemical Structure
  61. GC46163 IT-143B A bacterial metabolite IT-143B Chemical Structure
  62. GC41645 Jacaric Acid

    8(Z),10(E),12(Z)-Octadecatrienoic Acid

     Jacaric acid is a conjugated polyunsaturated fatty acid first isolated from seeds of Jacaranda plants. Jacaric Acid Chemical Structure
  63. GC41236 Kazusamycin A

    CL 1,957B, Hydroxyelactocin, Hydroxyleptomycin B, PD 114721

     Kazusamycin A is an antibiotic from Streptomyces and a hydroxy analog of Leptomycin B that demonstrates cytotoxic activity against various human and mouse tumor lines. Kazusamycin A Chemical Structure
  64. GC44009 KM 233 KM 233 es un cannabinoide clÁsico con buena penetraciÓn en la barrera hematoencefÁlica. KM 233 posee una afinidad selectiva por los receptores CB2 en relaciÓn con el THC. KM 233 es eficaz para reducir la carga tumoral del glioma U87 y se puede utilizar para la investigaciÓn del glioma. KM 233 Chemical Structure
  65. GC41627 Kumbicin C Kumbicin C es un compuesto bencenoide de bis-indolilo de un hongo del suelo australiano, Aspergillus kumbius. Kumbicin C Chemical Structure
  66. GC74503 KY-1044

    Alomfilimab; SAR 445256

     KY-1044 (Alomfilimab; SAR 445256) es un anticuerpo IgG1 totalmente humano que apunta al receptor coestimulinducible (ICOS). KY-1044 Chemical Structure
  67. GC47533 L-778,123 A dual inhibitor of FTase and GGTase I L-778,123 Chemical Structure
  68. GC47572 L-Lysine lactam (hydrochloride)

    L-(-)-α-Amino-ε-caprolactam, (S)-3-Amino-2-azepanone

     A building block L-Lysine lactam (hydrochloride) Chemical Structure
  69. GC49368 L-Methionine-d3

    (S)-Methionine-d3

     L-Metionina-d3 es la L-Metionina marcada con deuterio. L-Methionine-d3 Chemical Structure
  70. GC44084 L-Selenocystine

    Seleno-L-cystine

     La L-selenocistina es un aminoÁcido con puente de diseleniuro. L-Selenocystine Chemical Structure
  71. GC49560 L6H21 L6H21, un derivado de la chalcona, es un inhibidor de la diferenciaciÓn mieloide 2 (MD-2) activo, potente y especÍfico por vÍa oral. L6H21 Chemical Structure
  72. GP10103 Laminin (925-933)

    CDPGYIGSR, Cys-Asp-Pro-Gly-Tyr-Ile-Gly-Ser-Arg

    Laminina (925-933) (CDPGYIGSR), es la secuencia de Laminina en la cadena B1.

     Laminin (925-933) Chemical Structure
  73. GC90822 LAU-0901

    Un antagonista del receptor PAF

     LAU-0901 Chemical Structure
  74. GC91993 Lavendamycin

    NSC 322370

     Lavendamycin es un metabolito bacterique se ha encontrado en S. lavendulae y tiene actividades antimicrobiy anticancerosas. Lavendamycin Chemical Structure
  75. GC66014 Lepidiline A La lepidilina A muestra actividad citotÓxica frente a las células HL-60 con una IC50 de 32,3 μM. Lepidiline A Chemical Structure
  76. GC66012 Lepidiline C La lepidilina C muestra actividad citotÓxica frente a las células HL-60 con una IC50 de 27,7 μM. Lepidiline C Chemical Structure
  77. GC47554 Letrozole-d4 Letrozol-d4 (CGS 20267-d4) es el deuterio etiquetado como Letrozol. Letrozol (CGS 20267) es un inhibidor no esteroideo de la aromatasa potente, selectivo, reversible y activo por vía oral, con una IC50 de 11,5 nM. El letrozol inhibe selectivamente la biosíntesis de estrógenos y puede utilizarse para la investigación del cáncer de mama. Letrozole-d4 Chemical Structure
  78. GC44050 Leucinostatin A

    P168

     La leucinostatina A (AntibiÓtico P168) es un nonapéptido que ejerce una notable actividad especialmente contra Candida albicans y Cryptococcus neoformans. Leucinostatin A Chemical Structure
  79. GC41107 Leukotriene B5

    LTB5

     Leukotriene B5 (LTB5) is a leukotriene with diverse biological activities. Leukotriene B5 Chemical Structure
  80. GC49020 Levomefolate-13C-d3

    L-Methyl Folate-13C-d3, 6S-5-Methyltetrahydrofolate-13C-d3, 6S-5-MTHF-13C-d3

     An internal standard for the quantification of levomefolate Levomefolate-13C-d3 Chemical Structure
  81. GC90981 Lipid 10

    Un lípido catiónico ionizable.

     Lipid 10 Chemical Structure
  82. GC90964 Lipid Catechol

    Un lípido utilizado en la formación de nanoensamblajes de prodrogas lipídicas.

     Lipid Catechol Chemical Structure
  83. GC91124 Lipid III-45

    Un lípido catiónico ionizable.

     Lipid III-45 Chemical Structure
  84. GC18789 Lobaric Acid Lobaric acid is a depsidone metabolite that has been isolated from Stereocaulon lichen species with antioxidant, antiproliferative, antiviral, and enzyme inhibitory activites. Lobaric Acid Chemical Structure
  85. GC48989 LTX-315 (trifluoroacetate salt) A synthetic cationic amphiphilic peptide LTX-315 (trifluoroacetate salt) Chemical Structure
  86. GC74687 Luteolin monohydrate Luteolin monohydrate es el monodrato de luteolina. Luteolin monohydrate Chemical Structure
  87. GC52314 Lysyllysyllysine (trifluoroacetate salt)

    Trilysine

     A tripeptide Lysyllysyllysine (trifluoroacetate salt) Chemical Structure
  88. GC19775 M2N12 M2N12 es un inhibidor potente y altamente selectivo de la proteÍna fosfatasa 25C (Cdc25C) del ciclo de divisiÓn celular con un valor IC50 de 0,09 μM. M2N12 también tiene una actividad prometedora contra Cdc25A y Cdc25B con valores IC50 de 0,53 μM y 1,39 μM, respectivamente. M2N12 tiene actividad antitumoral y puede usarse para la investigaciÓn del cÁncer. M2N12 Chemical Structure
  89. GC41185 MAGL Inhibitor Compound 23 MAGL Inhibitor Compound 23 es un inhibidor potente, selectivo, reversible y competitivo de MAGL, con una IC50 de 80 nM. El compuesto inhibidor de MAGL 23 exhibe efectos antiproliferativos contra las células de cÁncer de mama, colorrectal y de ovario humanos. El compuesto inhibidor de MAGL 23 bloquea MAGL en ensayos basados en células e in vivo. MAGL Inhibitor Compound 23 Chemical Structure
  90. GC46031 Malabaricone B

    NSC 287967, NSC 630196

     La malabaricona B, un fenÓlico vegetal natural, es un inhibidor de la glucosidasa alfa activo por vÍa oral con una IC50 de 63,7 μM. Malabaricone B Chemical Structure
  91. GC44118 Malvidin (chloride)

    Syringidin

     Malvidin (cloruro) es un compuesto bioactivo aislado de Oryza sativacv. Heugjinjubyeo. Malvidin muestra citotoxicidad a través de la detención de la fase G2/M del ciclo celular y la inducción de la apoptosis. Malvidin se puede utilizar para la investigación del cáncer. Malvidin (chloride) Chemical Structure
  92. GC44126 Manzamine A

    Keramamine A

     Manzamine A is a β-carboline alkaloid with diverse activities that has been found in marine sponges, including X. Manzamine A Chemical Structure
  93. GP10140 MAP kinase fragment [Multiple species]

    H2N-Lys-Tyr-Ile-His-Ser-Ala-Asn-Val-Leu-OH

    MAP kinase fragment [Multiple species] Chemical Structure
  94. GC74475 Mapatumumab

    HGS-ETR1; Anti-Human TNFRSF10A Recombinant Antibody

     Mapatumumab (HGS-ETR1) es un anticuerpo monoclonal agonista IgG1 totalmente humano que se dirige al receptor 1 (TRAIL-R1) relacionado con el factor de necrosis tumoral que induce apoptosis. Mapatumumab Chemical Structure
  95. GC91980 MCI-INI-3 MCI-INI-3 es un inhibidor de la aldehído deshidrogenasa 1A3 (ALDH1A3; Ki = 0,55 μM). MCI-INI-3 Chemical Structure
  96. GC44168 Metanephrine

    DL-Metanephrine

    Metanephrine is a metabolite of epinephrine produced by the action of catechol-O-methyl transferase on epinephrine.

     Metanephrine Chemical Structure
  97. GC49423 Metanephrine-d3 (hydrochloride)

    DL-Metanephrine-d3

     An internal standard for the quantification of metanephrine Metanephrine-d3 (hydrochloride) Chemical Structure
  98. GC49879 Metformin hydroxy analog 2

    N-Carbonylguanidine

     An oxidation product of metformin Metformin hydroxy analog 2 Chemical Structure
  99. GC48805 Methapyrilene (hydrochloride) El clorhidrato de metapirileno (tenilpiramina) es un antihistamínico receptor H1 activo por vía oral y un agente anticolinérgico de la clase química de la piridina. Methapyrilene (hydrochloride) Chemical Structure
  100. GC47649 Methotrexate (hydrate)

    Amethopterin, CL 14,377, EMT 25299, MTX, NSC 740, R 9985

     A folic acid and aminopterin derivative Methotrexate (hydrate) Chemical Structure
  101. GC47650 Methotrexate-d3

    Amethopterin-d3, MTX-d3

     An internal standard for the quantification of methotrexate Methotrexate-d3 Chemical Structure

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