Basic information
- Standard SMILES
Clc1ccc2c(c1)N=C(N1CCNCC1)c1ccccc1N2- InChIKey
JNNOSTQEZICQQP-UHFFFAOYSA-N- Molecular formula
- C17H17ClN4
- Average molar mass
- 312.8 g/mol
- Monoisotopic mass
- 312.11417422
Overview
N-desmethylclozapine is a dibenzodoazepine substituted with chloro and piperazino groups which is a major metabolite of clozapine; a potent and selective 5-HT2C serotonin receptor antagonist. It has a role as a metabolite, a serotonergic antagonist and a delta-opioid receptor agonist. It is a member of piperazines, an organochlorine compound and a dibenzodiazepine.
Names & identifiers
- Preferred name
- N-Desmethylclozapine
- IUPAC
- 3-chloro-6-piperazin-1-yl-11H-benzo[b][1,4]benzodiazepine
- English name
- N-Desmethylclozapine
- Molecular formula
- C17H17ClN4
- Molecular weight
- 312.8
Names & synonyms
Show more names
Database identifiers
- CAS
6104-71-8- PubChem CID
- 135409468
- DTXSID
DTXSID0042616- ChEMBL
CHEMBL845- ChEBI
CHEBI:64050- UNII
- 1I9001LWY8
- EC Number
- 636-421-7
- Nikkaji
- J3.754.591K、J446.142H
Properties
Computed structural properties
- XLogP
- 2.6
- Topological polar surface area
- 39.7 Ų
- Hydrogen bond donors
- 2
- Hydrogen bond acceptors
- 3
- Rotatable bonds
- 1
- Heavy atoms
- 22
- Formal charge
- 0
- Complexity
- 421
Experimental & physicochemical properties
Drugs
Pharmaceuticals -> Antipsychotics
Pharmaceuticals -> Metabolite of Clozapine
Physicochemical properties
- Melting point
- 120 · 120-125°C
- Boiling point
- 502.6 · 502.6±60.0 °C(Predicted)
- Density
- 1.38 · 1.38±0.1 g/cm3(Predicted)
- Flash point
- 9 ℃ · 9℃
- storage temp.
- Store at RT
- solubility
- Chloroform (Slightly), DMSO, Methanol (Slightly)
- form
- Yellow solid.
- pka
- 8.49 · 8.49±0.10(Predicted)
- color
- Light Yellow to Yellow
- InChI
- 1S/C17H17ClN4/c18-12-5-6-15-16(11-12)21-17(22-9-7-19-8-10-22)13-3-1-2-4-14(13)20-15/h1-6,11,19-20H,7-10H2
- InChIKey
- JNNOSTQEZICQQP-UHFFFAOYSA-N
- SMILES
- Clc1ccc2Nc3ccccc3C(=Nc2c1)N4CCNCC4
- CAS DataBase Reference
- 6104 · 6104-71-8(CAS DataBase Reference)
- FDA UNII
- 1 I9001LWY8 · 1I9001LWY8
- UNSPSC Code
- 41116107 · 41116107
- NACRES
- 77 · NA.77
- Symbol(GHS)
- 7 · GHS07
- Signal word
- Warning
- Hazard statements
- 302 · H302+H332-H315-H319-H335
- Precautionary statements
- 261 · P261-P264-P301+P312-P302+P352-P304+P340+P312-P305+P351+P338
- target organs
- Respiratory system
- PPE
- 95 · dust mask type N95 (US), Eyeshields, Gloves
- Hazard Codes
- Xn,T,F
- Risk Statements
- 20 · 20/22-36/37/38-39/23/24/25-23/24/25-11
- Safety Statements
- 22 · 22-36-45-36/37-16-7
- RIDADR
- 3249 · 3249
- WGK Germany
- 3 · 3
- HazardClass
- 6.1 · 6.1(b)
- PackingGroup
- III
- Storage Class
- 11 · 11 - Combustible Solids
- Hazard Classifications
- 4 OralEye · Acute Tox. 4 OralEye Irrit. 2Skin Irrit. 2STOT SE 3
Safety & regulation
GHS classification
GHS Classification
Warning
H302 (95.1%): Harmful if swallowed [Warning Acute toxicity, oral]
P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 41 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard information
Safety data
- PPE
- dust mask type N95 (US), Eyeshields, Gloves
- wgk
- 3
- ridadr
- 3249
- risk_code
- 20/22-36/37/38-39/23/24/25-23/24/25-11
- Signal word
- Warning
- Symbol(GHS)
- GHS07
- hazard_code
- Xn,T,F
- safety_code
- 22-36-45-36/37-16-7
- hazard_class
- 6.1(b)
- Storage Class
- 11 - Combustible Solids
- packing_group
- III
- target organs
- Respiratory system
- Hazard statements
- H302+H332-H315-H319-H335
- Hazard Classifications
- Acute Tox. 4 OralEye Irrit. 2Skin Irrit. 2STOT SE 3
- Precautionary statements
- P261-P264-P301+P312-P302+P352-P304+P340+P312-P305+P351+P338
Chemistry & industry
Pharmacology
Pharmacodynamics
ACP-104 is a small molecule drug candidate we are developing as a novel therapy for schizophrenia. It is known that large amounts of ACP-104, or N-desmethylclozapine, are formed in the body after administration of clozapine. That is, clozapine is metabolized to ACP-104. We discovered that ACP-104 has a unique ability to stimulate m1 muscarinic receptors, a key muscarinic receptor. The m1 muscarinic receptors are widely known to play an important role in cognition. Since clozapine itself blocks the m1 muscarinic receptor, patients need to extensively metabolize clozapine into ACP-104 to stimulate this receptor and thereby overcome the blocking action of clozapine. Administration of ACP-104 will avoid the variability of this metabolic process and the competing action of clozapine. Like clozapine, ACP-104 is a dopamine antagonist and a 5-HT2A inverse agonist. We believe that ACP-104 represents a new approach to schizophrenia therapy that combines an atypical antipsychotic efficacy profile with the added advantage of beneficial cognitive effects.
Mechanism of Action
ACP-104 combines M1 muscarinic agonism, 5-HT2A inverse agonism, and D2 and D3 dopamine partial agonism in a single compound. ACP-104 uniquely stimulates brain cells known as M1 muscarinic receptors that play an important role in cognition. ACP-104 is a partial-agonist that causes weak activation of dopamine D2 and D3 receptors. These partial agonist properties of ACP-104 may lead to less motoric side effects than seen with most other antipsychotic drugs.
MeSH Pharmacological Classification
Agents that control agitated psychotic behavior, alleviate acute psychotic states, reduce psychotic symptoms, and exert a quieting effect. They are used in SCHIZOPHRENIA; senile dementia; transient psychosis following surgery; or MYOCARDIAL INFARCTION; etc. These drugs are often referred to as neuroleptics alluding to the tendency to produce neurological side effects, but not all antipsychotics are likely to produce such effects. Many of these drugs may also be effective against nausea, emesis, and pruritus.
Uses & manufacturing
Applications
UsesA major metabolite of Clozapine. A potent and selective 5-HT2C serotonin receptor antogonist.
UsesN-Desmethylclozapine has been used as standard to quantify the clozapine plasma levels in treatment-refractory Chinese schizophrenic patients.
UsesA major metabolite of Clozapine (C587500). A potent and selective 5-HT2C serotonin receptor antogonist.
General DescriptionN-Desmethylclozapine is an active metabolite of Clozapine, an atypical antipsychotic drug used for treatment of schizophrenia. Clozapine is sold under the trade names Clozaril and FrazaClo in the US. This Certified Snap-N-Spike Solution is suitable for use in urine drug testing, clinical toxicology, forensic analysis, and clinical monitoring by LC-MS/MS or GC/MS.
Upstream & downstream products
Upstream raw materials
Suppliers50 total
Additional notes
DefinitionChEBI: A dibenzodoazepine substituted with chloro and piperazino groups which is a major metabolite of clozapine; a potent and selective 5-HT2C serotonin receptor antagonist.
Related reactions
No reaction records under the current filter.
Linked notes
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