What compounds target MU-TYPE?

BiohacksAI has identified 65 compounds that interact with MU-TYPE (Mu-type opioid receptor (human)). Top compounds include: Morphine, Fentanyl, Astemizole Antihistamine drug now withdrawn from, Naloxone, Domperidone. Each compound is ranked by evidence score derived from PubMed bioassay confidence and assay count.

What is MU-TYPE (Mu-type opioid receptor)?

MU-TYPE is Mu-type opioid receptor (human). It is a molecular target for 65 compounds documented in PubMed bioassay data. UniProt ID: P35372.

MU-TYPE

MOLECULAR TARGET

Mu-type opioid receptor (human)

UniProt: P3537265 compounds

MU-TYPE (Mu-type opioid receptor (human)) is targeted by 65 compounds in the BiohacksAI evidence corpus, derived from PubMed bioassay data. Each compound is ranked by confidence score (log-normalized assay count × evidence quality).

Compounds Targeting MU-TYPE

Ranked by bioassay confidence score (PubChem active assay count × evidence quality).

#	Compound	Confidence	Active Assays
1	Morphine	2.20	8
2	Fentanyl	2.08	7
3	Astemizole Antihistamine drug now withdrawn from	1.79	5
4	Naloxone	1.79	5
5	Domperidone	1.61	4
6	Quetiapine Fumarate	1.39	3
7	Cinnarizine	1.39	3
8	Clotrimazole	1.39	3
9	Flunarizine Flunarizine is	1.39	3
10	Levorphanol	1.39	3
11	Promethazine	1.39	3
12	Reserpine	1.39	3
13	Amoxapine	1.10	2
14	Carvedilol	1.10	2
15	cinacalcet	1.10	2
16	Codeine	1.10	2
17	Disulfiram	1.10	2
18	Econazole	1.10	2
19	hydrocodone	1.10	2
20	Meperidine	1.10	2
21	Miconazole	1.10	2
22	Nalbuphine	1.10	2
23	oxatomide [Supplementary Concept] structure;	1.10	2
24	Tamsulosin	1.10	2
25	Sertraline	0.69	1
26	Amitriptyline Tricyclic antidepressant with anticholinergic and sedative properties. It appears to prevent	0.69	1
27	Aripiprazole	0.69	1
28	Benzethonium Bactericidal cationic quaternary ammonium surfactant used as	0.69	1
29	Bromocriptine	0.69	1
30	Butorphanol	0.69	1
31	candesartan cilexetil [Supplementary Concept]	0.69	1
32	Caspofungin	0.69	1
33	Danazol	0.69	1
34	Dequalinium	0.69	1
35	Dextromethorphan Methyl analog of DEXTRORPHAN that shows high affinity binding to several regions of	0.69	1
36	Dihydroergotamine	0.69	1
37	Dimethindene	0.69	1
38	Emetine	0.69	1
39	Physostigmine	0.69	1
40	Estrone	0.69	1
41	ethopropazine	0.69	1
42	Fluspirilene	0.69	1
43	Guanabenz	0.69	1
44	Hexachlorophene	0.69	1
45	Labetalol	0.69	1
46	Levallorphan	0.69	1
47	Loratadine	0.69	1
48	Loxapine	0.69	1
49	Meptazinol	0.69	1
50	Metergoline	0.69	1

Showing top 50 of 65 compounds. Use the BiohacksAI search to explore all MU-TYPE modulators.

About MU-TYPE as a Drug Target

MU-TYPE (Mu-type opioid receptor (human)) is a well-characterized molecular target in biomedical research. BiohacksAI tracks 65 compounds with documented MU-TYPE interaction from PubChem bioassay data, cross-referenced with PubMed clinical evidence. The confidence score reflects the log-normalized count of active PubChem assays, weighted by evidence quality from the BiohacksAI corpus.

MU-TYPE inhibitors, activators, and modulators are of interest in research areas including longevity, metabolic health, and neurological function. Each compound profile includes evidence score, RCT count, human study ratio, research velocity, and domain relevance.