Azacyclonol

Modify Date: 2025-08-22 06:48:19

Azacyclonol structure	Common Name	Azacyclonol
	CAS Number	115-46-8	Molecular Weight	267.365
	Density	1.1±0.1 g/cm3	Boiling Point	445.5±40.0 °C at 760 mmHg
	Molecular Formula	C₁₈H₂₁NO	Melting Point	160-163 °C
	MSDS	N/A	Flash Point	142.0±18.0 °C

Use of Azacyclonol

Azacyclonol, also known as γ-pipradol, is a drug used to diminish hallucinations in psychotic individuals.Target: OthersAzacyclonol is a drug which is a so-called ataractive, or agent which diminishes hallucinations in psychotic individuals. The formation of Azacyclonol in human intestinal microsomes is linear with respect to time up to 60 min. The rates of formation of Azacyclonol increases linearly with microsomal protein concentration up to 2 mg/mL. The apparent Km and Vmax values of Azacyclonol are 0.82 μM and 60 pmol/min/mg protein in microsomes from human liver [1]. The formation of Azacyclonol and terfenadine alcohol from terfenadine is confirmed to be catalyzed predominantly by CYP3A(4) isozyme, and the ratio of the rate of terfenadine alcohol formation to that of Azacyclonol is 3:1 [2]. The amount of Azacyclonol eliminated renally increases on average 2-fold after rifampin dosing [3].

Name	Diphenyl(piperidin-4-yl)methanol
Synonym	More Synonyms

Description	Azacyclonol, also known as γ-pipradol, is a drug used to diminish hallucinations in psychotic individuals.Target: OthersAzacyclonol is a drug which is a so-called ataractive, or agent which diminishes hallucinations in psychotic individuals. The formation of Azacyclonol in human intestinal microsomes is linear with respect to time up to 60 min. The rates of formation of Azacyclonol increases linearly with microsomal protein concentration up to 2 mg/mL. The apparent Km and Vmax values of Azacyclonol are 0.82 μM and 60 pmol/min/mg protein in microsomes from human liver [1]. The formation of Azacyclonol and terfenadine alcohol from terfenadine is confirmed to be catalyzed predominantly by CYP3A(4) isozyme, and the ratio of the rate of terfenadine alcohol formation to that of Azacyclonol is 3:1 [2]. The amount of Azacyclonol eliminated renally increases on average 2-fold after rifampin dosing [3].
Related Catalog	Signaling Pathways >> Others >> Others Research Areas >> Neurological Disease
References	[1]. Raeissi, S.D., et al., Comparison of CYP3A activities in a subclone of Caco-2 cells (TC7) and human intestine. Pharm Res, 1997. 14(8): p. 1019-25. [2]. Ling, K.H., et al., Metabolism of terfenadine associated with CYP3A(4) activity in human hepatic microsomes. Drug Metab Dispos, 1995. 23(6): p. 631-6. [3]. Brown, D.A. and J.P. Quilliam, The effects of some centrally acting drugs on ganglionic transmission in the cat. Br J Pharmacol Chemother, 1964. 23(2): p. 241-56.

Description

Related Catalog

Signaling Pathways >> Others >> Others

Research Areas >> Neurological Disease

References

[1]. Raeissi, S.D., et al., Comparison of CYP3A activities in a subclone of Caco-2 cells (TC7) and human intestine. Pharm Res, 1997. 14(8): p. 1019-25.

[2]. Ling, K.H., et al., Metabolism of terfenadine associated with CYP3A(4) activity in human hepatic microsomes. Drug Metab Dispos, 1995. 23(6): p. 631-6.

[3]. Brown, D.A. and J.P. Quilliam, The effects of some centrally acting drugs on ganglionic transmission in the cat. Br J Pharmacol Chemother, 1964. 23(2): p. 241-56.

Density	1.1±0.1 g/cm3
Boiling Point	445.5±40.0 °C at 760 mmHg
Melting Point	160-163 °C
Molecular Formula	C₁₈H₂₁NO
Molecular Weight	267.365
Flash Point	142.0±18.0 °C
Exact Mass	267.162323
PSA	32.26000
LogP	3.25
Vapour Pressure	0.0±1.1 mmHg at 25°C
Index of Refraction	1.584
InChIKey	ZMISODWVFHHWNR-UHFFFAOYSA-N
SMILES	OC(c1ccccc1)(c1ccccc1)C1CCNCC1

Azacyclonol MSDS(Chinese)

CHEMICAL IDENTIFICATION

RTECS NUMBER :: TN0470000

CHEMICAL NAME :: 4-Piperidinemethanol, alpha,alpha-diphenyl-

CAS REGISTRY NUMBER :: 115-46-8

BEILSTEIN REFERENCE NO. :: 0230221

LAST UPDATED :: 199612

DATA ITEMS CITED :: 4

MOLECULAR FORMULA :: C18-H21-N-O

MOLECULAR WEIGHT :: 267.40

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Oral

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 650 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: PSCBAY Psychopharmacology Service Center, Bulletin. (Bethesda, MD) V.1-3, 1961-65. For publisher information, see PSYBB9. Volume(issue)/page/year: 2,17,1963

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intraperitoneal

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 220 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: PSCBAY Psychopharmacology Service Center, Bulletin. (Bethesda, MD) V.1-3, 1961-65. For publisher information, see PSYBB9. Volume(issue)/page/year: 2,17,1963

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Subcutaneous

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 350 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: PSCBAY Psychopharmacology Service Center, Bulletin. (Bethesda, MD) V.1-3, 1961-65. For publisher information, see PSYBB9. Volume(issue)/page/year: 2,17,1963

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intravenous

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 177 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: PSCBAY Psychopharmacology Service Center, Bulletin. (Bethesda, MD) V.1-3, 1961-65. For publisher information, see PSYBB9. Volume(issue)/page/year: 2,17,1963

Hazard Codes	Xi:Irritant
Risk Phrases	R36/37/38
Safety Phrases	S24/25
RTECS	TN0470000
HS Code	29333999

Precursor 10
CAS#:114399-88-1 α,α-diphenyl-1-... CAS#:96067-93-5 4-(HYDROXY-DIPH... CAS#:108-20-3 Isopropyl ether CAS#:112818-77-6 ethyl 4-(hydrox...
CAS#:108-86-1 Bromobenzene CAS#:24228-40-8 Ethyl 1-benzyl-... CAS#:1126-09-6 Ethyl Isonipecotate CAS#:160809-38-1 Ethyl N-Cbz-pip...
CAS#:1620-30-0 Diphenyl(4-pyri... CAS#:6071-92-7 (1-methylpiperi...
DownStream 10
CAS#:105955-84-8 4-[4-[hydroxy(d... CAS#:50706-57-5 4-benzhydrylide... CAS#:50679-08-8 Terfenadine CAS#:19841-73-7 Piperidine,4-(d...
CAS#:83799-24-0 Fexofenadine CAS#:154477-55-1 Methyl 2-(4-(4-... CAS#:154825-96-4 Methyl 2-(4-(1-... CAS#:169280-33-5 ETHYL 4-[4-[4-(...
CAS#:43076-30-8 4'-tert-butyl-4... CAS#:5704-22-3 N-(1,3-benzodio...

HS Code	2933399090
Summary	2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Name: Primary qHTS assay for inhibitors of alpha-synuclein gene (SNCA) expression
Source: NCGC
External Id: SNCA-p-activity-luciferase

Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN

Name: Cytochrome P450 Family 1 Subfamily A Member 2 (CYP1A2) small molecule antagonists: lu...
Source: 824
External Id: CYP273

Name: Fluorescence-based cell-based primary high throughput screening assay to identify pos...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_PAM_FLUO8_1536_1X%ACT PRUN

Name: qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity
Source: NCGC
External Id: HERG01

Name: qHTS for Inhibitors of TGF-b: Cytotox Counterscreen
Source: NCGC
Target: N/A
External Id: SMAD3201

Name: uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay
Source: Burnham Center for Chemical Genomics
Target: cystic fibrosis transmembrane conductance regulator [Homo sapiens]
External Id: SBCCG-A764-CF-PAF-Primary-Assay

Name: Fluorescence-based cell-based primary high throughput screening assay to identify ant...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_ANT_FLUO8_1536_1X%INH PRUN

Name: qHTS for Inhibitors of TGF-b
Source: NCGC
Target: Smad3 [Homo sapiens]
External Id: SMAD3101

Name: qHTS Assay for Identifying Compounds that block Entry of Ebola Virus, Screen 2 green ...
Source: NCGC
Target: N/A
External Id: Ebola screen2_EMI141217_green

Total 402, Current Page 1 of 41

alpha,alpha-Diphenyl-4-piperidinomethanol

4-(α,α Diphenyl) piperidine methanol

Diphenyl(4-piperidinyl)methanol

a,a-Diphenyl-4-piperidinemethanol

γ-Pipradrol

MFCD00066980

Ataractan

α,α-Diphenyl-4-piperidinemethanol

α-(4-Piperidyl)benzhydrol

azacyclonol

diphenyl(4-piperidyl)methanol

Psychosan

g-Pipradrol

diphenyl(piperidin-4-yl)methanol

α,α-Diphenyl-4-piperidinomethanol

Diphenyl (g-Pyridyl)carbinol

a-(4-Piperidyl)benzhydrol

4-(Diphenylhydroxymethyl)piperidine

EINECS 204-092-5

Calmeran

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Product Name: Alpha,alpha-Diphenyl-4-piperidinomethanol
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Henan Tianfu Chemical Co., Ltd.
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Product Name: Diphenyl(piperidin-4-yl)methanol
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Purity: 99.0%
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Azacyclonol

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