(2S)-1-chloro-3-(2-methyl-5-nitroimidazol-1-yl)propan-2-ol
AlkaPlorer ID: AK413896
Synonym: None
IUPAC Name: (2S)-1-chloro-3-(2-methyl-5-nitroimidazol-1-yl)propan-2-ol
Structure
SMILES: CC1=NC=C([N+](=O)[O-])N1C[C@H](O)CCl
InChI: InChI=1S/C7H10ClN3O3/c1-5-9-3-7(11(13)14)10(5)4-6(12)2-8/h3,6,12H,2,4H2,1H3/t6-/m1/s1
InChIKey: IPWKIXLWTCNBKN-ZCFIWIBFSA-N
Reference
α-Glucosidase inhibitors and phytotoxins from <i>Streptomyces xanthophaeus</i>
PubChem CID: 6541429
LOTUS: LTS0263549
SuperNatural Ⅲ: SN0152084-02
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Streptomyces xanthophaeus | Streptomyces | Streptomycetaceae | Kitasatosporales | Actinomycetes | Actinomycetota | None | Bacteria |
Properties Information
Molecule Weight: 219.628
TPSA？: 81.19
MolLogP？: 0.6994199999999999
Number of H-Donors: 1
Number of H-Acceptors: 5
RingCount: 1
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|---|---|---|---|---|
| Homo sapiens | Cytochrome P450 1A2 | AC50 | nan | None | None |
| Homo sapiens | Cytochrome P450 2C19 | AC50 | nan | None | None |
| Homo sapiens | Cytochrome P450 2C9 | AC50 | nan | None | None |
| Homo sapiens | Cytochrome P450 2D6 | AC50 | nan | None | None |
| Homo sapiens | Cytochrome P450 3A4 | AC50 | nan | None | None |
| Rattus norvegicus | Peripheral myelin protein 22 | Potency | 17359.8 | nM | None |