| Display title | Chemistry:KML-010 |
| Default sort key | KML-010 |
| Page length (in bytes) | 2,096 |
| Namespace ID | 3022 |
| Namespace | Chemistry |
| Page ID | 811409 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of redirects to this page | 0 |
| Counted as a content page | Yes |
| Page image |  |
| HandWiki item ID | None |
| Edit | Allow all users (infinite) |
| Move | Allow all users (infinite) |
| Page creator | imported>WikiGary |
| Date of page creation | 10:12, 2 May 2023 |
| Latest editor | imported>WikiGary |
| Date of latest edit | 10:12, 2 May 2023 |
| Total number of edits | 1 |
| Recent number of edits (within past 90 days) | 0 |
| Recent number of distinct authors | 0 |
Description | Content |
Article description: (description)
This attribute controls the content of the description and og:description elements. | KML-010 is a drug derived from spiperone. It functions as a highly selective 5-HT2A receptor antagonist, with negligible affinity for the 5-HT1A or 5-HT2C receptors, and over 400-fold lower affinity for the D2 receptor in comparison to spiperone. |
