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2-carboxybenzoyl amlodipine

chemical compound
ChemicalSubstance group_of_stereoisomers Q27281765
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Summary

2-carboxybenzoyl amlodipine is a group of stereoisomers[1].

Key Facts

  • 2-carboxybenzoyl amlodipine's instance of is recorded as group of stereoisomers[2].
  • 2-carboxybenzoyl amlodipine's CAS Registry Number is recorded as 318465-73-5[3].
  • 2-carboxybenzoyl amlodipine's EC number is recorded as 608-671-7[4].
  • 2-carboxybenzoyl amlodipine's canonical SMILES is recorded as CCOC(=O)C1=C(NC(=C(C1C2=CC=CC=C2Cl)C(=O)OC)C)COCCNC(=O)C3=CC=CC=C3C(=O)O[5].
  • 2-carboxybenzoyl amlodipine's InChI is recorded as InChI=1S/C28H29ClN2O8/c1-4-39-28(36)24-21(15-38-14-13-30-25(32)17-9-5-6-10-18(17)26(33)34)31-16(2)22(27(35)37-3)23(24)19-11-7-8-12-20(19)29/h5-12,23,31H,4,13-15H2,1-3H3,(H,30,32)(H,33,34)[6].
  • 2-carboxybenzoyl amlodipine's InChIKey is recorded as IAYRABGXHCLELQ-UHFFFAOYSA-N[7].
  • 2-carboxybenzoyl amlodipine's chemical formula is recorded as C₂₈H₂₉ClN₂O₈[8].
  • 2-carboxybenzoyl amlodipine's subclass of is recorded as chemical compound[9].
  • 2-carboxybenzoyl amlodipine's UNII is recorded as K05668IG9G[10].
  • 2-carboxybenzoyl amlodipine's ChemSpider ID is recorded as 8113238[11].
  • 2-carboxybenzoyl amlodipine's PubChem CID is recorded as 9937612[12].
  • 2-carboxybenzoyl amlodipine's isomeric SMILES is recorded as O=C(O)C1=CC=CC=C1C(=O)NCCOC\C\2=C(/C(=O)OCC)\C(\C(=C(/N2)\C)\C(=O)OC)C3=CC=CC=C3Cl[13].
  • 2-carboxybenzoyl amlodipine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+556.161'}[14].
  • 2-carboxybenzoyl amlodipine's ECHA Substance Infocard ID is recorded as 100.121.792[15].
  • 2-carboxybenzoyl amlodipine's SureChEMBL ID is recorded as 7397399[16].
  • 2-carboxybenzoyl amlodipine's DSSTox substance ID is recorded as DTXSID301103092[17].
  • 2-carboxybenzoyl amlodipine's UniChem compound ID is recorded as 24206188[18].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [4] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . PubChem. Retrieved . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  10. [11] ↑ . ChemSpider. Retrieved . wikidata.org.
  11. [12] ↑ . PubChem. Retrieved . wikidata.org.
  12. [13] ↑ . ChemSpider. Retrieved . wikidata.org.
  13. [14] ↑ . PubChem. Retrieved . wikidata.org.
  14. [15] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). 2-carboxybenzoyl amlodipine. Retrieved May 3, 2026, from https://4ort.xyz/entity/2-carboxybenzoyl-amlodipine
MLA “2-carboxybenzoyl amlodipine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/2-carboxybenzoyl-amlodipine.
BibTeX @misc{4ortxyz_2-carboxybenzoyl-amlodipine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{2-carboxybenzoyl amlodipine}}, year = {2026}, url = {https://4ort.xyz/entity/2-carboxybenzoyl-amlodipine}, note = {Accessed: 2026-05-03}}
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