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NSC 718781-<sup>13</sup>C<sub>6</sub>

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Autophagy (2) EGFR (2) Isotope-Labeled Compounds (1)
By Research Areas:	Cancer (2)
Click Chemistry:	Alkynes (2)

2

Inhibitors & Agonists

2

Isotope-Labeled Compounds

2

Click Chemistry

Targets Recommended: P-glycoprotein

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

Erlotinib-13C6 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].

Erlotinib-13C6 hydrochloride 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.

Cat. No.	Product Name	Chemical Structure

Erlotinib-13C6
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].

Erlotinib-13C6 hydrochloride
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.

Cat. No.	Product Name		Classification

Erlotinib-13C6 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].

Erlotinib-13C6 hydrochloride 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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