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Details

Stereochemistry RACEMIC
Molecular Formula C14H20N2O2
Molecular Weight 248.3213
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PINDOLOL

SMILES

CC(C)NCC(COc1cccc2c1cc[nH]2)O

InChI

InChIKey=JZQKKSLKJUAGIC-UHFFFAOYSA-N
InChI=1S/C14H20N2O2/c1-10(2)16-8-11(17)9-18-14-5-3-4-13-12(14)6-7-15-13/h3-7,10-11,15-17H,8-9H2,1-2H3

HIDE SMILES / InChI

Description
Curator's Comment:: Description was created based on several sources, including: https://www.ncbi.nlm.nih.gov/pubmed/2879589 http://www.ncbi.nlm.nih.gov/pubmed/6125094 https://www.ncbi.nlm.nih.gov/pubmed/9536453 https://www.ncbi.nlm.nih.gov/pubmed/2429847 http://www.accessdata.fda.gov/drugsatfda_docs/label/2007/018285s034lbl.pdf

Pindolol was developed at Sandoz at 1960s. Pindolol is a nonselective beta-adrenergic antagonist (beta-blocker) which possesses intrinsic sympathomimetic activity (partial agonist activity) in therapeutic dosage ranges but does not possess quinidine-like membrane stabilizing activity. The partial beta-adrenergic agonistic activity of pindolol in the heart appears to be completely restricted to the sinoatrial pacemaker. In standard pharmacologic tests in man and animals, Pindolol attenuates increases in heart rate, systolic blood pressure, and cardiac output resulting from exercise and isoproterenol administration, thus confirming its beta-blocking properties. In addition to beta-adrenergic activity pindolol demonstrates mixed agonist-antagonist activity at central 5-HT receptors. Although in accordance with the hypothesis that pindolol increases the antidepressant effects of selective serotonin reuptake inhibitors by antagonism of 5-HT at inhibitory 5-HT1A autoreceptors, pindolol possesses partial agonist activity at 5-HT1A receptors. Pindolol tablets are indicated in the management of hypertension.

Originator

Sources: Innovation in the Pharmaceutical Industry: The Process of Drug Discovery and Development. Takuji Hara. Edward Elgar Publishing, 2003. ISBN 1843760509 p.76

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
6.4 nM [Ki]
9.25 null [pKd]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
VISKEN

Approved Use

Pindolol tablets are indicated in the management of hypertension. It may be used alone or concomitantly with other antihypertensive agents, particularly with a thiazide-type diuretic.

Launch Date

3.99859188E11
Primary
PINDOLOL

Approved Use

Pindolol tablets are indicated in the management of hypertension. It may be used alone or concomitantly with other antihypertensive agents, particularly with a thiazide-type diuretic.

Launch Date

7.1539202E11
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
250 nM
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PINDOLOL plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
1200 nM × h
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PINDOLOL plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
3.1 h
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PINDOLOL plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Other AEs: Bizarre dreams, Dizziness...
Other AEs:
Bizarre dreams (5%)
Dizziness (9%)
Fatigue (8%)
Hallucinations (<1%)
Insomnia (10%)
Nervousness (7%)
Weakness (4%)
Paresthesia (3%)
Dyspnea (5%)
Edema (6%)
Heart failure (<1%)
Palpitations (<1%)
Chest pain (3%)
Joint pain (7%)
Muscle cramps (3%)
Muscle pain (10%)
Abdominal discomfort (4%)
Nausea (5%)
Pruritus (1%)
Rash (<1%)
Anxiety (uncertain, <2%)
Lethargy (uncertain, <2%)
Visual disturbances (uncertain, <2%)
Hyperhidrosis (uncertain, <2%)
Bradycardia (uncertain, <2%)
Claudication (uncertain, <2%)
Cold extremities (uncertain, <2%)
Heart block (uncertain, <2%)
Syncope (uncertain, <2%)
Tachycardia (uncertain, <2%)
Weight gain (uncertain, <2%)
Hypotension (uncertain, <2%)
Diarrhea (uncertain, <2%)
Vomiting (uncertain, <2%)
Wheezing (uncertain, <2%)
Impotence (uncertain, <2%)
Pollakiuria (uncertain, <2%)
Eye discomfort (uncertain, <2%)
Sources:
AEs

AEs

AESignificanceDosePopulation
Pruritus 1%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Insomnia 10%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Muscle pain 10%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Chest pain 3%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Muscle cramps 3%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Paresthesia 3%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Abdominal discomfort 4%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Weakness 4%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Bizarre dreams 5%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Dyspnea 5%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Nausea 5%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Edema 6%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Joint pain 7%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Nervousness 7%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Fatigue 8%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Dizziness 9%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Hallucinations <1%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Heart failure <1%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Palpitations <1%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Rash <1%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Anxiety uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Bradycardia uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Claudication uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Cold extremities uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Diarrhea uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Eye discomfort uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Heart block uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Hyperhidrosis uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Hypotension uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Impotence uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Lethargy uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Pollakiuria uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Syncope uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Tachycardia uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Visual disturbances uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Vomiting uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Weight gain uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Wheezing uncertain, <2%
5 mg 2 times / day steady, oral (starting)
Recommended
Dose: 5 mg, 2 times / day
Route: oral
Route: steady
Dose: 5 mg, 2 times / day
Sources:
unhealthy
Health Status: unhealthy
Condition: Hypertension
Sources:
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG


OverviewOther

Other InhibitorOther SubstrateOther Inducer




Drug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
yes
Drug as victim

Drug as victim

TargetModalityActivityMetaboliteClinical evidence
yes
yes
yes
yes (co-administration study)
Comment: cimetidine coadministration increases pindolol plasma levels
yes
yes (co-administration study)
Comment: cimetidine increased AUC by 1.4 fold and Cmax by 1.3 fold
yes
yes (co-administration study)
Comment: cimetidine increased AUC by 1.4 fold and Cmax by 1.3 fold
PubMed

PubMed

TitleDatePubMed
Effects of prindolol on isoproterenol-induced subendocardial ischaemia in dogs with multiple chronic coronary artery occlusion.
1975 Jul
Pindolol antagonises G-protein activation at both pre- and postsynaptic serotonin 5-HT1A receptors: a.
2001 Apr
Cataleptic effect of neurosteroid 3alpha-hydroxy-5alpha-pregnan-20-one in mice: modulation by serotonergic agents.
2001 Apr 13
Quantitative structure-retention and retention-activity relationships of beta-blocking agents by micellar liquid chromatography.
2001 Apr 6
Flesinoxan, a 5-HT1A receptor agonist/alpha 1-adrenoceptor antagonist, lowers intraocular pressure in NZW rabbits.
2001 Aug
Monocyte 5-HT1A receptors mediate pindobind suppression of natural killer cell activity: modulation by catalase.
2001 Feb
Discriminative stimulus effects of centrally administered isoproterenol in rats: mediation by beta-1 adrenergic receptors.
2001 Feb
Abolition of (-)-CGP 12177-evoked cardiostimulation in double beta1/beta2-adrenoceptor knockout mice. Obligatory role of beta1-adrenoceptors for putative beta4-adrenoceptor pharmacology.
2001 Jan
The 'dalhousie serotonin cocktail' for treatment-resistant major depressive disorder.
2001 Jun
Effect of lipophilicity on in vivo iontophoretic delivery. II. Beta-blockers.
2001 Jun
Characterization of sarcolemma and sarcoplasmic reticulum isolated from skeletal muscle of the freeze tolerant wood frog, Rana sylvatica: the beta(2)-adrenergic receptor and calcium transport systems in control, frozen and thawed states.
2001 Jun
New methods for the isolation of skeletal muscle sarcolemma and sarcoplasmic reticulum allowing a comparison between the mammalian and amphibian beta(2)-adrenergic receptors and calcium pumps.
2001 Jun
The inhibitory effect of serotonin on the spontaneous discharge of suprachiasmatic neurons in hypothalamic slice is mediated by 5-HT(7) receptor.
2001 Mar 1
How does pindolol improve antidepressant action?
2001 May
Chiral separation of beta-blockers after derivatization with (-)-alphamethoxy-alpha-(trifluoromethyl)phenylacetyl chloride by gas chromatography.
2001 Oct
The 5-HT1A receptor agonist 8-hydroxy-2-di-n-(propylamino)tetralin (8-OH-DPAT) induces hyperglucagonemia in rats.
2001 Oct
Pindolol potentiation of paroxetine for generalized social phobia: a double-blind, placebo-controlled, crossover study.
2001 Oct
Separation of basic drug enantiomers by capillary electrophoresis using ovoglycoprotein as a chiral selector: comparison of chiral resolution ability of ovoglycoprotein and completely deglycosylated ovoglycoprotein.
2001 Sep
Factors affecting fluvoxamine antidepressant activity: influence of pindolol and 5-HTTLPR in delusional and nondelusional depression.
2001 Sep 1
Management of treatment-refractory panic disorder.
2001 Spring
[Pharmacology of beta blockers and their significance for therapy of hypertension].
2002 Aug
[Reactions between dialkylamine drugs, 2,3-dichloro-1,4-naphthoquinone and acetaldehyde].
2002 Aug
Serotonergic control of cerebellar mossy fiber activity by modulation of signal transfer by rat pontine nuclei neurons.
2002 Aug
Enantioselectivity in the steady-state pharmacokinetics and transplacental distribution of pindolol at delivery in pregnancy-induced hypertension.
2002 Aug
Melatonin potentiates 5-HT(1A) receptor activation in rat hypothalamus and results in hypothermia.
2002 Aug
Altered expression of autonomic neurotransmitter receptors and proliferative responses in lymphocytes from a chronic mild stress model of depression: effects of fluoxetine.
2002 Aug
Indorenate produces antidepressant-like actions in the rat forced swimming test via 5-HT1A receptors.
2002 Dec
The role of in vivo molecular imaging with PET and SPECT in the elucidation of psychiatric drug action and new drug development.
2002 Dec
Serotonin regulates hippocampal glucocorticoid receptor expression via a 5-HT7 receptor.
2002 Dec 15
Methiothepin attenuates gastric secretion and motility effects of vagal stimulants at the dorsal vagal complex.
2002 Feb 1
Reconsideration of 5-hydroxytryptamine (5-HT)(7) receptor distribution using [(3)H]5-carboxamidotryptamine and [(3)H]8-hydroxy-2-(di-n-propylamino)tetraline: analysis in brain of 5-HT(1A) knockout and 5-HT(1A/1B) double-knockout mice.
2002 Jul
Synthesis and evaluation of (S)-[18F]-fluoroethylcarazolol for in vivo beta-adrenoceptor imaging in the brain.
2002 Jul
The neuropharmacology of serotonin and noradrenaline in depression.
2002 Jun
[Effect of (+/-)-pindolol on the central 5-HT1A receptor by the use of in vivo microdialysis and hippocampal slice preparations].
2002 Jun
Management of treatment resistant obsessive-compulsive disorder. Algorithms for pharmacotherapy.
2002 Jun
Somatodendritic action of pindolol to attenuate the paroxetine-induced decrease in serotonin release from the rat ventral hippocampus: a microdialysis study.
2002 May
Simultaneous determination of eight beta-blockers by gradient high-performance liquid chromatography with combined ultraviolet and fluorescence detection in corneal permeability studies in vitro.
2002 May 25
Familial left ventricular hypertrabeculation in two blind brothers.
2002 May-Jun
Involvement of 5-HT7 receptors in serotonergic effects on spike afterpotentials in presumed jaw-closing motoneurons of rats.
2002 Nov 8
Spin trapping study of reactive oxygen species formation during bopindolol peroxidation.
2002 Oct 15
Antibody capture assay reveals bell-shaped concentration-response isotherms for h5-HT(1A) receptor-mediated Galpha(i3) activation: conformational selection by high-efficacy agonists, and relationship to trafficking of receptor signaling.
2002 Sep
Pharmacological management for agitation and aggression in people with acquired brain injury.
2003
Evidence against beta 3-adrenoceptors or low affinity state of beta 1-adrenoceptors mediating relaxation in rat isolated aorta.
2003 Jan
Evidence that the anorexia induced by lipopolysaccharide is mediated by the 5-HT2C receptor.
2003 Jan
Chiral separation of amines with N-benzoxycarbonylglycyl-L-proline as selector in non-aqueous capillary electrophoresis using methanol and 1,2-dichloroethane in the background electrolyte.
2003 Jan 17
EEG effects of buspirone and pindolol: a method of examining 5-HT1A receptor function in humans.
2003 Mar
Effects on sleep architecture of pindolol, paroxetine and their combination in healthy volunteers.
2003 Mar
Anxiolytic-like effects of baicalein and baicalin in the Vogel conflict test in mice.
2003 Mar 19
Patents

Sample Use Guides

The recommended initial dose of pindolol tablets is 5 mg b.i.d. alone or in combination with other antihypertensive agents. An antihypertensive response usually occurs within the first week of treatment. Maximal response, however, may take as long as or occasionally longer than 2 weeks. If a satisfactory reduction in blood pressure does not occur within 3 to 4 weeks, the dose may be adjusted in increments of 10 mg/day at these intervals up to a maximum of 60 mg/day.
Route of Administration: Oral
In Vitro Use Guide
Pindolol (1-10 uM) blocked the catecholamine-induced augmentation of late after-discharge (LAD) (postganglionic branches or ganglion cells of the paravertebral sympathetic chain of the bullfrog were used in vitro)
Name Type Language
PINDOLOL
EP   HSDB   INN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
USAN   INN  
Official Name English
NSC-757276
Code English
4-(2-HYDROXY-3-ISOPROPYLAMINOPROPOXY)INDOLE
Systematic Name English
PINDOLOL COMPONENT OF VISKAZIDE
Common Name English
PINDOLOL [JAN]
Common Name English
PECTOBLOC
Brand Name English
DL-LB-46
Common Name English
(RS)-PINDOLOL
Common Name English
DL-PINDOLOL
Common Name English
2-PROPANOL, 1-(1H-INDOL-4-YLOXY)-3-(1-METHYLETHYL)AMINO-
Systematic Name English
PINDOLOL [MI]
Common Name English
PYNASTIN
Common Name English
PINDOLOL [HSDB]
Common Name English
PINDOLOL [EP MONOGRAPH]
Common Name English
PINDOLOL [USAN]
Common Name English
PINDOLOL [WHO-DD]
Common Name English
LB-46
Code English
DECRETEN
Common Name English
4-(3-ISOPROPYLAMINO-2-HYDROXYPROPOXY)INDOLE
Systematic Name English
VISKAZIDE COMPONENT PINDOLOL
Common Name English
1-((1-METHYLETHYL)AMINO)-3-(4-INDOLYLOXY)-2-PROPANOL
Systematic Name English
CARVISKEN
Brand Name English
PINDOLOL [VANDF]
Common Name English
PINBETOL
Common Name English
(+/-)-PINDOLOL
Common Name English
PRINODOLOL
Common Name English
1-(INDOL-4-YLOXY)-3-(ISOPROPYLAMINO)-2-PROPANOL
Systematic Name English
PINDOLOL [USP MONOGRAPH]
Common Name English
CALVISKEN
Brand Name English
PINDOLOL [MART.]
Common Name English
GLAUCO-VISKEN
Common Name English
APO-PINDOL
Common Name English
BLOCKLIN-L
Brand Name English
N-(2-HYDROXY-3-(1H-INDOL-4-YLOXY)PROPYL)-N-ISOPROPYLAMINE
Systematic Name English
PINDOLOL [USP-RS]
Common Name English
PINDOLOL [INN]
Common Name English
PINDOLOL [ORANGE BOOK]
Common Name English
DL-4-(2-HYDROXY-3-(ISOPROPYLAMINO)PROPOXY)INDOLE
Common Name English
(+/-)-4-(2-HYDROXY-3-(ISOPROPYLAMINO)PROPOXY)INDOLE
Systematic Name English
DURAPINDOL
Common Name English
VISKEN
Brand Name English
BETAPINDOL
Common Name English
(+/-)-LB-46
Code English
2-PROPANOL, 1-(INDOL-4-YLOXY)-3-(ISOPROPYLAMINO)-
Systematic Name English
Classification Tree Code System Code
WHO-VATC QC07AA03
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
LIVERTOX 778
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
NCI_THESAURUS C29576
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
NDF-RT N0000000161
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
WHO-VATC QC07CA03
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
WHO-ATC C07CA03
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
NDF-RT N0000175556
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
WHO-ATC C07AA03
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
Code System Code Type Description
FDA UNII
BJ4HF6IU1D
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
RXCUI
8332
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY RxNorm
DRUG BANK
DB00960
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
MESH
D010869
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
EPA CompTox
13523-86-9
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
DRUG CENTRAL
2176
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
INN
2698
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
MERCK INDEX
M8824
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY Merck Index
LACTMED
Pindolol
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
NCI_THESAURUS
C47673
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
HSDB
6539
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
WIKIPEDIA
PINDOLOL
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
ECHA (EC/EINECS)
236-867-9
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
ChEMBL
CHEMBL500
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
USP_CATALOG
1539701
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY USP-RS
PUBCHEM
4828
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
CAS
13523-86-9
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
EVMPD
SUB09854MIG
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY
IUPHAR
91
Created by admin on Fri Jun 25 21:00:59 UTC 2021 , Edited by admin on Fri Jun 25 21:00:59 UTC 2021
PRIMARY