Dichlorochromopyrrolic acid (CHEM103135)
| Record Information | |||||||||
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| Version | 1.0 | ||||||||
| Creation Date | 2026-04-05 13:43:59 UTC | ||||||||
| Update Date | 2026-08-21 20:32:35 UTC | ||||||||
| Accession Number | CHEM103135 | ||||||||
| Identification | |||||||||
| Common Name | Dichlorochromopyrrolic acid | ||||||||
| Class | Small Molecule | ||||||||
| Description | Dichlorochromopyrrolic acid is an organic compound with the formula C22H13Cl2N3O4 and an average molecular weight of 454.26 g/mol. Dichlorochromopyrrolic acid belongs to the indoles, a subclass of indoles and derivatives within the organic compounds. Within its classification, it is categorized as an organoheterocyclic compound. Regarding its biological activity, there is one recorded protein target for this compound, which is Cytochrome P450 (staP). | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C22H13Cl2N3O4 | ||||||||
| Average Molecular Mass | 454.260 g/mol | ||||||||
| Monoisotopic Mass | 453.028 g/mol | ||||||||
| CAS Registry Number | 537041-76-2 | ||||||||
| IUPAC Name | 3,4-bis(7-chloro-1H-indol-3-yl)-1H-pyrrole-2,5-dicarboxylic acid | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | OC(=O)C1=C(C2=CNC3=C2C=CC=C3Cl)C(=C(N1)C(O)=O)C1=CNC2=C1C=CC=C2Cl | ||||||||
| InChI Identifier | InChI=1S/C22H13Cl2N3O4/c23-13-5-1-3-9-11(7-25-17(9)13)15-16(20(22(30)31)27-19(15)21(28)29)12-8-26-18-10(12)4-2-6-14(18)24/h1-8,25-27H,(H,28,29)(H,30,31) | ||||||||
| InChI Key | OAMCCJASDLMTOO-UHFFFAOYSA-N | ||||||||
| Chemical Taxonomy | |||||||||
| Classification | Not classified | ||||||||
| Biological Properties | |||||||||
| Status | Detected and Not Quantified | ||||||||
| Origin | Not Available | ||||||||
| Cellular Locations | Not Available | ||||||||
| Biofluid Locations | Not Available | ||||||||
| Tissue Locations | Not Available | ||||||||
| Pathways | Not Available | ||||||||
| Applications | Not Available | ||||||||
| Biological Roles | Not Available | ||||||||
| Chemical Roles | Not Available | ||||||||
| Physical Properties | |||||||||
| State | Not Available | ||||||||
| Appearance | Not Available | ||||||||
| Experimental Properties |
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| Predicted Properties | Not Available | ||||||||
| Spectra | |||||||||
| Spectra |
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| Toxicity Profile | |||||||||
| Route of Exposure | Not Available | ||||||||
| Mechanism of Toxicity | Not Available | ||||||||
| Metabolism | Not Available | ||||||||
| Toxicity Values | Not Available | ||||||||
| Lethal Dose | Not Available | ||||||||
| Carcinogenicity (IARC Classification) | Not Available | ||||||||
| Uses/Sources | Not Available | ||||||||
| Minimum Risk Level | Not Available | ||||||||
| Health Effects | Not Available | ||||||||
| Symptoms | Not Available | ||||||||
| Treatment | Not Available | ||||||||
| Concentrations | |||||||||
| Not Available | |||||||||
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| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||
