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Compound Detail

CHEMBL2146146

ATROPINE SULFATE
💊 Approved Drug
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💊 Approved Drug
CN1[C@@H]2CC[C@H]1C[C@@H](OC(=O)C(CO)c1ccccc1)C2.O=S(=O)(O)O

Basic Information

ChEMBL ID CHEMBL2146146
Name ATROPINE SULFATE
Phase Approved
Structure Type MOL
InChI Key VJFQPODMEGSXHC-RIMUKSHESA-N
Therapeutic ✓ Yes
Parent Compound CHEMBL517712
Active Moiety CHEMBL517712

Known Names

Atropine sulfate Atropine sulfate anhydrous Atropine sulfate ansyr plastic syringe Atropine sulfate component of colonaid Atropine sulfate component of di-atro Atropine sulfate component of enlon-plus Atropine sulfate component of lo-trol Atropine sulfate component of logen Atropine sulfate component of lomanate Atropine sulfate component of lomotil Atropine sulfate component of lonox Atropine sulfate component of low-quel +12 more
3
Targets
5
Activities
2
Assay Types
0
PK Parameters
20
Publications
24
Known Names
8
Indications
3
Mechanisms

Molecular Properties

289.4
MW (Da)
1.93
ALogP
4
HBA
1
HBD
49.8
PSA (Ų)
0.86
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
First Approval 1960
Availability Prescription
Chirality Racemic

Routes of Administration

Oral Parenteral Topical
USAN Stem -trop-

Extended Properties

Molecular Formula C17H25NO7S
MW 387.45
Aromatic Rings 1
Heavy Atoms 21
NP-Likeness 0.79

Mechanism of Action

Mechanism Action Type Target Direct Efficacy
Muscarinic acetylcholine receptor M3 antagonist ANTAGONIST Muscarinic acetylcholine receptor M3
Muscarinic acetylcholine receptor M1 antagonist ANTAGONIST Muscarinic acetylcholine receptor M1
Muscarinic acetylcholine receptor M2 antagonist ANTAGONIST Muscarinic acetylcholine receptor M2

Indications

Mydriasis Parkinson Disease Peptic Ulcer Rhinitis, Allergic, Seasonal Rhinitis, Allergic, Seasonal Myopia Organophosphate Poisoning Postoperative Complications

Activity Summary

Kd 3 meas. best 9.31
IC50 2 meas. best 5.3

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Kd 9.31 9.31 0.5 1
Cavia porcellus
CHEMBL369
Kd 9.06 7.64 0.9 2
Plasmodium falciparum
CHEMBL364
IC50 5.3 5.15 5011.9 2

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
533877 10.1021/jm00197a006 Mus musculus 3
6126589 10.1021/jm00350a018 Rattus norvegicus 3
6195312 10.1021/np50028a027 Enterococcus faecalis 2
- 10.6019/CHEMBL4495565 SARS-CoV-2 2
- 10.6019/CHEMBL4808148 Histone deacetylase 6 2
19734910 10.1038/nchembio.215 Plasmodium falciparum 2
6195312 10.1021/np50028a027 Saccharomyces cerevisiae 2
6195312 10.1021/np50028a027 Candida albicans 2
6195312 10.1021/np50028a027 Staphylococcus aureus 2
6195312 10.1021/np50028a027 Pseudomonas fluorescens 2
6195312 10.1021/np50028a027 Pseudomonas aeruginosa 2
6195312 10.1021/np50028a027 Escherichia coli 2
6102153 10.1021/jm00176a009 Cavia porcellus 2
7143364 10.1021/jm00352a029 Cavia porcellus 2
6195312 10.1021/np50028a027 Bacillus subtilis 1
3941416 10.1021/jm00151a002 Mus musculus 1
20022146 10.1016/j.ejmech.2009.11.034 Homo sapiens 1
7143364 10.1021/jm00352a029 Mus musculus 1
23062825 10.1016/j.bmc.2012.09.040 Acetylcholinesterase 1
23062825 10.1016/j.bmc.2012.09.040 Cholinesterase 1

Data from ChEMBL 36 via Core Engine