Search Result
Results for "
NSC-<sup>13</sup>C<sub>10</sub>,<sup>15</sup>N<sub>2</sub>
" in MedChemExpress (MCE) Product Catalog:
13
Isotope-Labeled Compounds
| Cat. No. |
Product Name |
Target |
Research Areas |
Chemical Structure |
-
- HY-N1150S9
-
|
DThyd-<sup>15sup>N<sub>2sub>; NSC-<sup>15sup>N<sub>2sub>
|
DNA/RNA Synthesis
Endogenous Metabolite
Orthopoxvirus
|
Cancer
|
|
Thymidine- 15N2 is the 15N labeled Thymidine[1]. Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication[2][3][4].
|
-
-
- HY-N1150S11
-
|
DThyd-<sup>13sup>C<sub>10sub>; NSC 21548-<sup>13sup>C<sub>10sub>
|
Isotope-Labeled Compounds
DNA/RNA Synthesis
Endogenous Metabolite
Orthopoxvirus
|
Cancer
|
|
Thymidine- 13C10 (DThyd- 13C10; NSC 21548- 13C10) is 13C-labeled Thymidine (HY-N1150). Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication.
|
-
-
- HY-A0161S
-
|
Clofedanol-<sup>13sup>C<sub>6sub>; Calmotusin-<sup>13sup>C<sub>6sub>; NSC 113595-<sup>13sup>C<sub>6sub>
|
Isotope-Labeled Compounds
|
Infection
|
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Chlophedianol- 13C6 is the 13C labeled Chlophedianol (HY-A0161). Chlophedianol is an orally active and potent antitussive agent. Chlophedianol can be used for the research of acute cough due to upper respiratory tract infections (URIs)[1][2][3].
|
-
-
- HY-N1150S8
-
|
DThyd-<sup>13sup>C<sub>10sub>,<sup>15sup>N<sub>2sub>; NSC-<sup>13sup>C<sub>10sub>,<sup>15sup>N<sub>2sub>
|
DNA/RNA Synthesis
Endogenous Metabolite
Orthopoxvirus
|
Cancer
|
|
Thymidine- 13C10, 15N2 is the 13C and 15N labeled Thymidine[1]. Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication[2][3][4].
|
-
-
- HY-50896S1
-
|
CP-358774-<sup>13sup>C<sub>6sub>; NSC 718781-<sup>13sup>C<sub>6sub>; OSI-774-<sup>13sup>C<sub>6sub>
|
Isotope-Labeled Compounds
EGFR
Autophagy
|
Cancer
|
|
Erlotinib- 13C6 is a 13C-labeled Erlotinib. Erlotinib is a directly acting EGFR tyrosine kinase inhibitor, with an IC50 of 2 nM for human EGFR[1].
|
-
-
- HY-12008S1
-
|
CP-358774-<sup>13sup>C<sub>6sub> hydrochloride; NSC 718781-<sup>13sup>C<sub>6sub> hydrochloride; OSI-774-<sup>13sup>C<sub>6sub> hydrochloride
|
EGFR
Autophagy
|
Cancer
|
|
Erlotinib- 13C6 (hydrochloride) is the 13C labeled Erlotinib Hydrochloride[1]. Erlotinib Hydrochloride (CP-358774 Hydrochloride) inhibits purified EGFR kinase with an IC50 of 2 nM[2]. Erlotinib-13C6 (hydrochloride) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
|
-
-
- HY-12033S1
-
|
2-ME2-<sup>13sup>C<sub>6sub>; NSC-659853-<sup>13sup>C<sub>6sub>
|
Isotope-Labeled Compounds
Microtubule/Tubulin
Reactive Oxygen Species
Apoptosis
Autophagy
Endogenous Metabolite
|
Cancer
|
|
2-Methoxyestradiol- 13C6 is the 13C-labeled 2-Methoxyestradiol. 2-Methoxyestradiol (2-ME2), an orally active endogenous metabolite of 17β-estradiol (E2), is an apoptosis inducer and an angiogenesis inhibitor with potent antineoplastic activity. 2-Methoxyestradiol also destablize microtubules. 2-Methoxyestradio, also a potent superoxide dismutase (SOD) inhibitor and a ROS-generating agent, induces autophagy in the transformed cell line HEK293 and the cancer cell lines U87 and HeLa[1][2][3][4][5][6].
|
-
-
- HY-N0055S
-
|
3-O-Caffeoylquinic acid-<sub>13sub>C<sup>3sup>; Heriguard-<sub>13sub>C<sup>3sup>; NSC-407296-<sub>13sub>C<sup>3sup>
|
Isotope-Labeled Compounds
|
Cancer
|
|
Chlorogenic acid- 13C3 (Heriguard- 13C3; NSC-407296- 13C3) is 13C- and 15N-labeled Chlorogenic acid (HY-N0055). Chlorogenic acid is a major phenolic compound in Lonicera japonica Thunb.. It plays several important and therapeutic roles such as antioxidant activity, antibacterial, hepatoprotective, cardioprotective, anti-inflammatory, antipyretic, neuroprotective, anti-obesity, antiviral, anti-microbial, anti-hypertension .
|
-
-
- HY-B0457S2
-
|
Chlorimipramine-<sup>13sup>C,d<sub>3sub> hydrochloride; G-34586-<sup>13sup>C,d<sub>3sub> hydrochloride; NSC-169865-<sup>13sup>C,d<sub>3sub> hydrochloride
|
Isotope-Labeled Compounds
Serotonin Transporter
|
Neurological Disease
|
|
Clomipramine- 13C,d3 (hydrochloride) is the 13C- and deuterium labeled Clomipramine (hydrochloride). Clomipramine (Chlorimipramine) hydrochloride is a potent 5-HT reuptake blocker with the IC50 value of 1.5 nM. Clomipramine hydrochloride is a tricyclic antidepressant that can be used for the research of depression and obsessive compulsive disorder (OCD)[1].
|
-
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- HY-N6746S1
-
|
NSC 186-<sup>13sup>C<sub>13
|
Isotope-Labeled Compounds
|
Cancer
|
|
Citrinin- 13C13 (NSC 186- 13C13) is the 13C labeled Citrinin (HY-N6746) . Citrinin is a mycotoxin which causes contamination in the food and is associated with different toxic effects. Citrinin is usually found together with another nephrotoxic mycotoxin, Ochratoxin A. Citrinin is also reported to possess a broad spectrum of bioactivities, including antibacterial, antifungal, and potential anticancer and neuro-protective effects in vitro .
|
-
-
- HY-N1393S
-
|
NSC 3778-<sup>13sup>C<sub>6sub>; O-Methylsalicylic acid-<sup>13sup>C<sub>6sub>; Salicylic acid methyl ether-<sup>13sup>C<sub>6sub>
|
Isotope-Labeled Compounds
Endogenous Metabolite
|
Cancer
|
|
2-Methoxybenzoic acid- 13C6 is the 13C-labeled 2-Methoxybenzoic acid. 2-Methoxybenzoic acid (NSC 3778) is used as an internal standard of salicylic acid and its putative biosynthetic precursors in cucumber leaves. Another known use is in the synthesis of Benextramine.
|
-
-
- HY-B0139S
-
|
5-Fluorocytosine-<sup>13sup>C,15sup>N<sub>2sub>; NSC 103805-<sup>13sup>C,15sup>N<sub>2sub>; Ro 2-9915-<sup>13sup>C,15sup>N<sub>2sub>
|
Isotope-Labeled Compounds
|
Infection
|
|
Flucytosine- 13C, 15N2 (NSC 103805- 13C, 15N2; Ro 2-9915- 13C, 15N2) is a 13C- and 15N-labeled Flucytosine (HY-B0139).
|
-
-
- HY-Y1250S6
-
|
Fmoc glycine-<sup>13sup>C<sub>2sub>,<sup>15sup>N; N-(9-Fluorenylmethoxycarbonyl)glycine-<sup>13sup>C<sub>2sub>,<sup>15sup>N; N-Fluorenylmethoxycarbonylglycine-<sup>13sup>C<sub>2sub>,<sup>15sup>N; NPC 14692-<sup>13sup>C<sub>2sub>-<sup>15sup>N; NSC 334288-<sup>13sup>C<sub>2sub>,<sup>15sup>N; [[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]acetic acid-<sup>13sup>C<sub>2sub>,<sup>15sup>N
|
Isotope-Labeled Compounds
Influenza Virus
Bacterial
|
Infection
|
|
Fmoc-Gly-OH- 13C2, 15N is a 15N-labeled and 13C-labled Crystal Violet. Crystal violet (Basic Violet 3) is a triarylmethane dye. Crystal Violet (Gentian Violet) has antiviral effects against H1N1 and also has prominent bactericidal activities.
|
-
| Cat. No. |
Product Name |
Chemical Structure |
-
- HY-N1150S9
-
|
|
|
Thymidine- 15N2 is the 15N labeled Thymidine[1]. Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication[2][3][4].
|
-
-
- HY-N1150S11
-
|
|
|
Thymidine- 13C10 (DThyd- 13C10; NSC 21548- 13C10) is 13C-labeled Thymidine (HY-N1150). Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication.
|
-
-
- HY-A0161S
-
|
|
|
Chlophedianol- 13C6 is the 13C labeled Chlophedianol (HY-A0161). Chlophedianol is an orally active and potent antitussive agent. Chlophedianol can be used for the research of acute cough due to upper respiratory tract infections (URIs)[1][2][3].
|
-
-
- HY-N1150S8
-
|
|
|
Thymidine- 13C10, 15N2 is the 13C and 15N labeled Thymidine[1]. Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication[2][3][4].
|
-
-
- HY-50896S1
-
|
|
|
Erlotinib- 13C6 is a 13C-labeled Erlotinib. Erlotinib is a directly acting EGFR tyrosine kinase inhibitor, with an IC50 of 2 nM for human EGFR[1].
|
-
-
- HY-12008S1
-
|
|
|
Erlotinib- 13C6 (hydrochloride) is the 13C labeled Erlotinib Hydrochloride[1]. Erlotinib Hydrochloride (CP-358774 Hydrochloride) inhibits purified EGFR kinase with an IC50 of 2 nM[2]. Erlotinib-13C6 (hydrochloride) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
|
-
-
- HY-12033S1
-
|
|
|
2-Methoxyestradiol- 13C6 is the 13C-labeled 2-Methoxyestradiol. 2-Methoxyestradiol (2-ME2), an orally active endogenous metabolite of 17β-estradiol (E2), is an apoptosis inducer and an angiogenesis inhibitor with potent antineoplastic activity. 2-Methoxyestradiol also destablize microtubules. 2-Methoxyestradio, also a potent superoxide dismutase (SOD) inhibitor and a ROS-generating agent, induces autophagy in the transformed cell line HEK293 and the cancer cell lines U87 and HeLa[1][2][3][4][5][6].
|
-
-
- HY-N0055S
-
|
|
|
Chlorogenic acid- 13C3 (Heriguard- 13C3; NSC-407296- 13C3) is 13C- and 15N-labeled Chlorogenic acid (HY-N0055). Chlorogenic acid is a major phenolic compound in Lonicera japonica Thunb.. It plays several important and therapeutic roles such as antioxidant activity, antibacterial, hepatoprotective, cardioprotective, anti-inflammatory, antipyretic, neuroprotective, anti-obesity, antiviral, anti-microbial, anti-hypertension .
|
-
-
- HY-B0457S2
-
|
|
|
Clomipramine- 13C,d3 (hydrochloride) is the 13C- and deuterium labeled Clomipramine (hydrochloride). Clomipramine (Chlorimipramine) hydrochloride is a potent 5-HT reuptake blocker with the IC50 value of 1.5 nM. Clomipramine hydrochloride is a tricyclic antidepressant that can be used for the research of depression and obsessive compulsive disorder (OCD)[1].
|
-
-
- HY-N6746S1
-
|
|
|
Citrinin- 13C13 (NSC 186- 13C13) is the 13C labeled Citrinin (HY-N6746) . Citrinin is a mycotoxin which causes contamination in the food and is associated with different toxic effects. Citrinin is usually found together with another nephrotoxic mycotoxin, Ochratoxin A. Citrinin is also reported to possess a broad spectrum of bioactivities, including antibacterial, antifungal, and potential anticancer and neuro-protective effects in vitro .
|
-
-
- HY-N1393S
-
|
|
|
2-Methoxybenzoic acid- 13C6 is the 13C-labeled 2-Methoxybenzoic acid. 2-Methoxybenzoic acid (NSC 3778) is used as an internal standard of salicylic acid and its putative biosynthetic precursors in cucumber leaves. Another known use is in the synthesis of Benextramine.
|
-
-
- HY-B0139S
-
|
|
|
Flucytosine- 13C, 15N2 (NSC 103805- 13C, 15N2; Ro 2-9915- 13C, 15N2) is a 13C- and 15N-labeled Flucytosine (HY-B0139).
|
-
-
- HY-Y1250S6
-
|
|
|
Fmoc-Gly-OH- 13C2, 15N is a 15N-labeled and 13C-labled Crystal Violet. Crystal violet (Basic Violet 3) is a triarylmethane dye. Crystal Violet (Gentian Violet) has antiviral effects against H1N1 and also has prominent bactericidal activities.
|
-
| Cat. No. |
Product Name |
|
Classification |
-
- HY-50896S1
-
|
CP-358774-<sup>13sup>C<sub>6sub>; NSC 718781-<sup>13sup>C<sub>6sub>; OSI-774-<sup>13sup>C<sub>6sub>
|
|
Alkynes
|
|
Erlotinib- 13C6 is a 13C-labeled Erlotinib. Erlotinib is a directly acting EGFR tyrosine kinase inhibitor, with an IC50 of 2 nM for human EGFR[1].
|
-
- HY-12008S1
-
|
CP-358774-<sup>13sup>C<sub>6sub> hydrochloride; NSC 718781-<sup>13sup>C<sub>6sub> hydrochloride; OSI-774-<sup>13sup>C<sub>6sub> hydrochloride
|
|
Alkynes
|
|
Erlotinib- 13C6 (hydrochloride) is the 13C labeled Erlotinib Hydrochloride[1]. Erlotinib Hydrochloride (CP-358774 Hydrochloride) inhibits purified EGFR kinase with an IC50 of 2 nM[2]. Erlotinib-13C6 (hydrochloride) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
|
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