Chemical Formula: C21H21N3O4

Chemical Formula C21H21N3O4

Found 17 metabolite its formula value is C21H21N3O4

Desmethyl Erlotinib

2-({4-[(3-ethynylphenyl)amino]-7-(2-methoxyethoxy)quinazolin-6-yl}oxy)ethan-1-ol

C21H21N3O4 (379.1532)


   

2-(4-(3-Ethynylanilino)-6-(2-methoxyethoxy)quinazolin-7-yl)oxyethanol

2-({4-[(3-ethynylphenyl)amino]-6-(2-methoxyethoxy)quinazolin-7-yl}oxy)ethan-1-ol

C21H21N3O4 (379.1532)


   

(+)-Cyclotryprostatin D

(+)-Cyclotryprostatin D

C21H21N3O4 (379.1532)


   

sceavodimerine C

sceavodimerine C

C21H21N3O4 (379.1532)


   

4-(9H-beta-carbolin-1-ylmethyl)-5-(1-hydroxy-ethyl)-6-oxo-1,4,5,6-tetrahydro-pyridine-3-carboxylic acid methyl ester|Hydroxylyalidin|Hydroxylyalidine

4-(9H-beta-carbolin-1-ylmethyl)-5-(1-hydroxy-ethyl)-6-oxo-1,4,5,6-tetrahydro-pyridine-3-carboxylic acid methyl ester|Hydroxylyalidin|Hydroxylyalidine

C21H21N3O4 (379.1532)


   

Angiotensin I-Converting Enzyme (ACE) Inactivator

Angiotensin I-Converting Enzyme (ACE) Inactivator

C21H21N3O4 (379.1532)


   

1-Benzyl-N-[(benzyloxy)carbonyl]-L-histidine

1-Benzyl-N-[(benzyloxy)carbonyl]-L-histidine

C21H21N3O4 (379.1532)


   

1-(2-AMINOPHENYL)ETHAN-1-ONEOXIME

1-(2-AMINOPHENYL)ETHAN-1-ONEOXIME

C21H21N3O4 (379.1532)


   

Desmethyl Erlotinib

2-((4-((3-Ethynylphenyl)amino)-7-(2-methoxyethoxy)quinazolin-6-yl)oxy)ethanol

C21H21N3O4 (379.1532)


   

1-(2-AMINO-PHENYL)-PIPERIDIN-3-CARBAMICACIDTERT-BUYTLESTER

1-(2-AMINO-PHENYL)-PIPERIDIN-3-CARBAMICACIDTERT-BUYTLESTER

C21H21N3O4 (379.1532)


   

6-[2-amino-5-(4-methoxyphenoxy)-1H-pyrimidin-6-ylidene]-3-(2-methylprop-2-enoxy)-1-cyclohexa-2,4-dienone

6-[2-amino-5-(4-methoxyphenoxy)-1H-pyrimidin-6-ylidene]-3-(2-methylprop-2-enoxy)-1-cyclohexa-2,4-dienone

C21H21N3O4 (379.1532)


   

ML381

ML381

C21H21N3O4 (379.1532)


ML381 (VU0488130) is a highly selective, central nervous system penetrant mAChR M5 orthogonal antagonist (IC50 = 450 nM; Ki = 340 nM). ML381 is unstable in rat plasma and can be mainly used as a molecular probe for in vitro and electrophysiological studies[1][2].

   

(8z)-1,10-dihydroxy-8-{[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene}-3-oxa-6,9-diazatricyclo[4.4.0.0²,⁴]dec-9-en-7-one

(8z)-1,10-dihydroxy-8-{[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene}-3-oxa-6,9-diazatricyclo[4.4.0.0²,⁴]dec-9-en-7-one

C21H21N3O4 (379.1532)


   

1-hydroxy-12-(2-methylprop-1-en-1-yl)-10,13,19-triazapentacyclo[11.7.0.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]icosa-3(11),4,6,8-tetraene-2,14,20-trione

1-hydroxy-12-(2-methylprop-1-en-1-yl)-10,13,19-triazapentacyclo[11.7.0.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]icosa-3(11),4,6,8-tetraene-2,14,20-trione

C21H21N3O4 (379.1532)


   

(6s,7r)-4-(methoxycarbonyl)-7-methyl-5h,6h,7h-cyclopenta[c]pyridin-6-yl (1r)-1-methyl-1,2-dihydro-2,7-naphthyridine-4-carboxylate

(6s,7r)-4-(methoxycarbonyl)-7-methyl-5h,6h,7h-cyclopenta[c]pyridin-6-yl (1r)-1-methyl-1,2-dihydro-2,7-naphthyridine-4-carboxylate

C21H21N3O4 (379.1532)


   

(1r,12s,15s)-1-hydroxy-12-(2-methylprop-1-en-1-yl)-10,13,19-triazapentacyclo[11.7.0.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]icosa-3(11),4,6,8-tetraene-2,14,20-trione

(1r,12s,15s)-1-hydroxy-12-(2-methylprop-1-en-1-yl)-10,13,19-triazapentacyclo[11.7.0.0³,¹¹.0⁴,⁹.0¹⁵,¹⁹]icosa-3(11),4,6,8-tetraene-2,14,20-trione

C21H21N3O4 (379.1532)


   

4-(methoxycarbonyl)-7-methyl-5h,6h,7h-cyclopenta[c]pyridin-6-yl 1-methyl-1,2-dihydro-2,7-naphthyridine-4-carboxylate

4-(methoxycarbonyl)-7-methyl-5h,6h,7h-cyclopenta[c]pyridin-6-yl 1-methyl-1,2-dihydro-2,7-naphthyridine-4-carboxylate

C21H21N3O4 (379.1532)