<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2016-05-25 18:14:34 UTC</creation_date>
  <update_date>2026-09-01 06:32:31 UTC</update_date>
  <accession/>
  <common_name>Angiotensin II</common_name>
  <class>SmallMolecule</class>
  <description>Angiotensin II (C50H71N13O12) belongs to the amino acids, peptides, and analogues, a subclass of carboxylic acids and derivatives within the organic compounds. With an average molecular weight of 1,046 g/mol, Angiotensin II is a heavy molecule. It acts as an agonist or inhibitor of two protein targets: the Type-1 angiotensin II receptor (AGTR1) and the Type-2 angiotensin II receptor (AGTR2).

The compound is found in or released from eight recorded sources, including electrical and electronic equipment such as antennas, television systems, gas filled discharge tubes with gaseous cathodes, and discharge tubes with liquid pool cathodes. Other sources include the preparation of wine or sparkling wine, the preparation of vinegar, other smoking requisites, and cardiac stimulants excluding cardiac glycosides. The recorded exposure route is intravenous.

Angiotensin II is associated with several health effects. It is linked to cardiomyopathy (PMC12712907), heart failure (PMC6210295), and hyperglycemia (PMC9368651). It is associated with inflammation (PMC12028762, PMC6273216) and an increase in atherosclerosis (PMC10889477, PMC11351257) and proteinuria (PMC3136362). Regarding blood pressure, the compound is associated with hypertension (PMC4302234, PMC6151556) and an increase in blood pressure (PMC11277057, PMC12146500, PMC12722972, PMC6567131), though it is also associated with a decrease in high blood pressure (PMC12028762).</description>
  <categories/>
  <types/>
  <synonyms/>
  <chemical_formula>C50H71N13O12</chemical_formula>
  <average_molecular_weight>1046.1786</average_molecular_weight>
  <monisotopic_moleculate_weight>1045.534514801</monisotopic_moleculate_weight>
  <iupac_name>(3S)-3-amino-3-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S,2S)-1-{[(2S)-1-[(2S)-2-{[(1S)-1-carboxy-2-phenylethyl]carbamoyl}pyrrolidin-1-yl]-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]carbamoyl}-2-methylbutyl]carbamoyl}-2-(4-hydroxyphenyl)ethyl]carbamoyl}-2-methylpropyl]carbamoyl}-4-[(diaminomethylidene)amino]butyl]carbamoyl}propanoic acid</iupac_name>
  <traditional_iupac>(3S)-3-amino-3-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S,2S)-1-{[(2S)-1-[(2S)-2-{[(1S)-1-carboxy-2-phenylethyl]carbamoyl}pyrrolidin-1-yl]-3-(3H-imidazol-4-yl)-1-oxopropan-2-yl]carbamoyl}-2-methylbutyl]carbamoyl}-2-(4-hydroxyphenyl)ethyl]carbamoyl}-2-methylpropyl]carbamoyl}-4-[(diaminomethylidene)amino]butyl]carbamoyl}propanoic acid</traditional_iupac>
  <cas_registry_number>11128-99-7</cas_registry_number>
  <smiles>CC[C@H](C)[C@H](NC(=O)[C@H](CC1=CC=C(O)C=C1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C(=O)N[C@@H](CC1=CN=CN1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O</smiles>
  <inchi>InChI=1S/C50H71N13O12/c1-5-28(4)41(47(72)59-36(23-31-25-54-26-56-31)48(73)63-20-10-14-38(63)45(70)60-37(49(74)75)22-29-11-7-6-8-12-29)62-44(69)35(21-30-15-17-32(64)18-16-30)58-46(71)40(27(2)3)61-43(68)34(13-9-19-55-50(52)53)57-42(67)33(51)24-39(65)66/h6-8,11-12,15-18,25-28,33-38,40-41,64H,5,9-10,13-14,19-24,51H2,1-4H3,(H,54,56)(H,57,67)(H,58,71)(H,59,72)(H,60,70)(H,61,68)(H,62,69)(H,65,66)(H,74,75)(H4,52,53,55)/t28-,33-,34-,35-,36-,37-,38-,40-,41-/m0/s1</inchi>
  <inchikey>CZGUSIXMZVURDU-JZXHSEFVSA-N</inchikey>
  <taxonomy>
    <kingdom>Organic compounds</kingdom>
    <super_class>Organic acids and derivatives</super_class>
    <class>Carboxylic acids and derivatives</class>
    <sub_class>Amino acids, peptides, and analogues</sub_class>
    <direct_parent>Oligopeptides</direct_parent>
    <alternate_parents>
      <alternative_parent>1-hydroxy-2-unsubstituted benzenoids</alternative_parent>
      <alternative_parent>Alpha amino acid amides</alternative_parent>
      <alternative_parent>Amino acids</alternative_parent>
      <alternative_parent>Amphetamines and derivatives</alternative_parent>
      <alternative_parent>Aspartic acid and derivatives</alternative_parent>
      <alternative_parent>Azacyclic compounds</alternative_parent>
      <alternative_parent>Carbonyl compounds</alternative_parent>
      <alternative_parent>Carboximidamides</alternative_parent>
      <alternative_parent>Carboxylic acids</alternative_parent>
      <alternative_parent>Dicarboxylic acids and derivatives</alternative_parent>
      <alternative_parent>Guanidines</alternative_parent>
      <alternative_parent>Heteroaromatic compounds</alternative_parent>
      <alternative_parent>Histidine and derivatives</alternative_parent>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>Imidazolyl carboxylic acids and derivatives</alternative_parent>
      <alternative_parent>Isoleucine and derivatives</alternative_parent>
      <alternative_parent>Monoalkylamines</alternative_parent>
      <alternative_parent>N-acyl amines</alternative_parent>
      <alternative_parent>N-acyl-L-alpha-amino acids</alternative_parent>
      <alternative_parent>N-acylpyrrolidines</alternative_parent>
      <alternative_parent>Organic oxides</alternative_parent>
      <alternative_parent>Organopnictogen compounds</alternative_parent>
      <alternative_parent>Phenylalanine and derivatives</alternative_parent>
      <alternative_parent>Phenylpropanoic acids</alternative_parent>
      <alternative_parent>Proline and derivatives</alternative_parent>
      <alternative_parent>Propargyl-type 1,3-dipolar organic compounds</alternative_parent>
      <alternative_parent>Pyrrolidinecarboxamides</alternative_parent>
      <alternative_parent>Secondary carboxylic acid amides</alternative_parent>
      <alternative_parent>Tertiary carboxylic acid amides</alternative_parent>
      <alternative_parent>Tyrosine and derivatives</alternative_parent>
      <alternative_parent>Valine and derivatives</alternative_parent>
    </alternate_parents>
    <substituents>
      <substituent>1-hydroxy-2-unsubstituted benzenoid</substituent>
      <substituent>3-phenylpropanoic-acid</substituent>
      <substituent>Alpha-amino acid amide</substituent>
      <substituent>Alpha-amino acid or derivatives</substituent>
      <substituent>Alpha-oligopeptide</substituent>
      <substituent>Amine</substituent>
      <substituent>Amino acid</substituent>
      <substituent>Amino acid or derivatives</substituent>
      <substituent>Amphetamine or derivatives</substituent>
      <substituent>Aromatic heteromonocyclic compound</substituent>
      <substituent>Aspartic acid or derivatives</substituent>
      <substituent>Azacycle</substituent>
      <substituent>Azole</substituent>
      <substituent>Benzenoid</substituent>
      <substituent>Carbonyl group</substituent>
      <substituent>Carboxamide group</substituent>
      <substituent>Carboximidamide</substituent>
      <substituent>Carboxylic acid</substituent>
      <substituent>Dicarboxylic acid or derivatives</substituent>
      <substituent>Fatty acyl</substituent>
      <substituent>Fatty amide</substituent>
      <substituent>Guanidine</substituent>
      <substituent>Heteroaromatic compound</substituent>
      <substituent>Histidine or derivatives</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Imidazole</substituent>
      <substituent>Imidazolyl carboxylic acid derivative</substituent>
      <substituent>Isoleucine or derivatives</substituent>
      <substituent>Monocyclic benzene moiety</substituent>
      <substituent>N-acyl-alpha amino acid or derivatives</substituent>
      <substituent>N-acyl-alpha-amino acid</substituent>
      <substituent>N-acyl-amine</substituent>
      <substituent>N-acyl-l-alpha-amino acid</substituent>
      <substituent>N-acylpyrrolidine</substituent>
      <substituent>N-substituted-alpha-amino acid</substituent>
      <substituent>Organic 1,3-dipolar compound</substituent>
      <substituent>Organic nitrogen compound</substituent>
      <substituent>Organic oxide</substituent>
      <substituent>Organic oxygen compound</substituent>
      <substituent>Organoheterocyclic compound</substituent>
      <substituent>Organonitrogen compound</substituent>
      <substituent>Organooxygen compound</substituent>
      <substituent>Organopnictogen compound</substituent>
      <substituent>Phenol</substituent>
      <substituent>Phenylalanine or derivatives</substituent>
      <substituent>Primary aliphatic amine</substituent>
      <substituent>Primary amine</substituent>
      <substituent>Proline or derivatives</substituent>
      <substituent>Propargyl-type 1,3-dipolar organic compound</substituent>
      <substituent>Pyrrolidine</substituent>
      <substituent>Pyrrolidine carboxylic acid or derivatives</substituent>
      <substituent>Pyrrolidine-2-carboxamide</substituent>
      <substituent>Secondary carboxylic acid amide</substituent>
      <substituent>Tertiary carboxylic acid amide</substituent>
      <substituent>Tyrosine or derivatives</substituent>
      <substituent>Valine or derivatives</substituent>
    </substituents>
    <molecular_framework>Aromatic heteromonocyclic compounds</molecular_framework>
    <descriptors>
      <descriptor>Angiotensin [KO:K09821]</descriptor>
      <descriptor>angiotensin II</descriptor>
    </descriptors>
  </taxonomy>
  <status>Detected and Not Quantified</status>
  <origin/>
  <cellular_locations/>
  <biofluid_locations/>
  <tissue_locations/>
  <pathways>
    <pathway>
      <name>Benazepril Action Pathway</name>
      <smpdb_id>SMP0000145</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Captopril Action Pathway</name>
      <smpdb_id>SMP0000146</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Cilazapril Action Pathway</name>
      <smpdb_id>SMP0000147</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Enalapril Action Pathway</name>
      <smpdb_id>SMP0000148</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Fosinopril Action Pathway</name>
      <smpdb_id>SMP0000149</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Lisinopril Action Pathway</name>
      <smpdb_id>SMP0000150</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Moexipril Action Pathway</name>
      <smpdb_id>SMP0000151</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Perindopril Action Pathway</name>
      <smpdb_id>SMP0000152</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Quinapril Action Pathway</name>
      <smpdb_id>SMP0000153</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Ramipril Action Pathway</name>
      <smpdb_id>SMP0000154</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Rescinnamine Action Pathway</name>
      <smpdb_id>SMP0000155</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Spirapril Action Pathway</name>
      <smpdb_id>SMP0000156</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Trandolapril Action Pathway</name>
      <smpdb_id>SMP0000157</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Candesartan Action Pathway</name>
      <smpdb_id>SMP0000158</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Eprosartan Action Pathway</name>
      <smpdb_id>SMP0000159</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Forasartan Action Pathway</name>
      <smpdb_id>SMP0000160</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Irbesartan Action Pathway</name>
      <smpdb_id>SMP0000161</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Losartan Action Pathway</name>
      <smpdb_id>SMP0000162</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Olmesartan Action Pathway</name>
      <smpdb_id>SMP0000163</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Telmisartan Action Pathway</name>
      <smpdb_id>SMP0000164</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Valsartan Action Pathway</name>
      <smpdb_id>SMP0000165</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Angiotensin Metabolism</name>
      <smpdb_id>SMP0000587</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Temocapril Action Pathway</name>
      <smpdb_id>SMP0000733</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Kidney Function - Ascending Limb of The Loop of Henle</name>
      <smpdb_id>SMP0121010</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Kidney Function - Collecting Duct</name>
      <smpdb_id>SMP0121011</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Kidney Function - Distal Convoluted Tubule</name>
      <smpdb_id>SMP0121012</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Aldosterone from Steroidogenesis</name>
      <smpdb_id>SMP0121126</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Benazepril ACE inhibitor Action Pathway</name>
      <smpdb_id>SMP0122803</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Cilazapril ACE inhibitor Action Pathway</name>
      <smpdb_id>SMP0122986</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Enalapril ACE Inhibitor Action Pathway</name>
      <smpdb_id>SMP0123086</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Fosinopril ACE Inhibitor Action Pathway</name>
      <smpdb_id>SMP0123090</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Lisinopril ACE Inhibitor</name>
      <smpdb_id>SMP0123091</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Moexipril ACE Inhibitor Action Pathway</name>
      <smpdb_id>SMP0123092</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Perindopril ACE Inhibitor Action Pathway</name>
      <smpdb_id>SMP0123093</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Quinapril ACE Inhibitor Action Pathway</name>
      <smpdb_id>SMP0123094</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Ramipril ACE Inhibitor Action Pathway</name>
      <smpdb_id>SMP0123095</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Trandolapril ACE Inhibitor Action Pathway</name>
      <smpdb_id>SMP0123104</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Losartan Angiotensin blocker Action Pathway</name>
      <smpdb_id>SMP0124963</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Candesartan Action Pathway (New)</name>
      <smpdb_id>SMP0124964</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Forasartan Angiotensin Blocker Action Pathway</name>
      <smpdb_id>SMP0124966</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Irbesartan Angiotensin blocker Action Pathway</name>
      <smpdb_id>SMP0124967</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Olmesartan ARB Action Pathway</name>
      <smpdb_id>SMP0124968</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Telmisartan Action Pathway (New)</name>
      <smpdb_id>SMP0124969</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Valsartan Action Pathway (New)</name>
      <smpdb_id>SMP0124970</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Fimasartan Action Pathway</name>
      <smpdb_id>SMP0125993</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Azilsartan medoxomil Action Pathway</name>
      <smpdb_id>SMP0126012</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Tasosartan Action Pathway</name>
      <smpdb_id>SMP0126013</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Saprisartan Action Pathway</name>
      <smpdb_id>SMP0126015</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Candesartan cilexetil Action Pathway</name>
      <smpdb_id>SMP0126016</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Zofenopril Action Pathway</name>
      <smpdb_id>SMP0126074</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>ACE</name>
      <smpdb_id>SMP0127068</smpdb_id>
      <kegg_map_id/>
    </pathway>
  </pathways>
  <state/>
  <appearance/>
  <experimental_properties>
    <property>
      <kind>logp</kind>
      <value>-1.7</value>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>logp</kind>
      <value>-0.87</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logs</kind>
      <value>-4.83</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>solubility</kind>
      <value>1.56e-02 g/l</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logp</kind>
      <value>-5.3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_acidic</kind>
      <value>3.15</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_basic</kind>
      <value>10.83</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>iupac</kind>
      <value>(3S)-3-amino-3-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S,2S)-1-{[(2S)-1-[(2S)-2-{[(1S)-1-carboxy-2-phenylethyl]carbamoyl}pyrrolidin-1-yl]-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]carbamoyl}-2-methylbutyl]carbamoyl}-2-(4-hydroxyphenyl)ethyl]carbamoyl}-2-methylpropyl]carbamoyl}-4-[(diaminomethylidene)amino]butyl]carbamoyl}propanoic acid</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>average_mass</kind>
      <value>1046.1786</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>1045.534514801</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>CC[C@H](C)[C@H](NC(=O)[C@H](CC1=CC=C(O)C=C1)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C(=O)N[C@@H](CC1=CN=CN1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C50H71N13O12</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C50H71N13O12/c1-5-28(4)41(47(72)59-36(23-31-25-54-26-56-31)48(73)63-20-10-14-38(63)45(70)60-37(49(74)75)22-29-11-7-6-8-12-29)62-44(69)35(21-30-15-17-32(64)18-16-30)58-46(71)40(27(2)3)61-43(68)34(13-9-19-55-50(52)53)57-42(67)33(51)24-39(65)66/h6-8,11-12,15-18,25-28,33-38,40-41,64H,5,9-10,13-14,19-24,51H2,1-4H3,(H,54,56)(H,57,67)(H,58,71)(H,59,72)(H,60,70)(H,61,68)(H,62,69)(H,65,66)(H,74,75)(H4,52,53,55)/t28-,33-,34-,35-,36-,37-,38-,40-,41-/m0/s1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>CZGUSIXMZVURDU-JZXHSEFVSA-N</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polar_surface_area</kind>
      <value>408.84</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>refractivity</kind>
      <value>269.81</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polarizability</kind>
      <value>107.02</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>rotatable_bond_count</kind>
      <value>29</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>acceptor_count</kind>
      <value>17</value>
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