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Details

Stereochemistry RACEMIC
Molecular Formula 2C10H19N3O2.H2O4S
Molecular Weight 524.632
Optical Activity ( + / - )
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GUANADREL SULFATE

SMILES

OS(O)(=O)=O.NC(=N)NCC1COC2(CCCCC2)O1.NC(=N)NCC3COC4(CCCCC4)O3

InChI

InChIKey=RTEVGQJRTFFMLL-UHFFFAOYSA-N
InChI=1S/2C10H19N3O2.H2O4S/c2*11-9(12)13-6-8-7-14-10(15-8)4-2-1-3-5-10;1-5(2,3)4/h2*8H,1-7H2,(H4,11,12,13);(H2,1,2,3,4)

HIDE SMILES / InChI

Molecular Formula C10H19N3O2
Molecular Weight 213.2768
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula H2O4S
Molecular Weight 98.078
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: Description was created based on several sources, including https://www.drugs.com/cons/guanadrel.html

Guanadrel is a postganglionic adrenergic blocking agent. Uptake of guanadrel and storage in sympathetic neurons occurs via the norepinephrine pump or transporter. Guanadrel slowly displaces norepinephrine from its storage in nerve endings and thereby blocks the release of norepinephrine normally produced by nerve stimulation. The reduction in neurotransmitter release in response to sympathetic nerve stimulation, as a result of catecholamine depletion, leads to reduced arteriolar vasoconstriction, especially the reflex increase in sympathetic tone that occurs with a change in position. Guanadrel is used to treat and control hypertension.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Hylorel

Approved Use

Used to treat high blood pressure (hypertension).

Launch Date

4.09881608E11
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
28.4 ng/mL
50 mg single, oral
dose: 50 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
GUANADREL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
42 ng/mL
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
GUANADREL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
73 ng/mL
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
GUANADREL plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
404.9 μg × h/mL
50 mg single, oral
dose: 50 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
GUANADREL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
234 ng × h/mL
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
GUANADREL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
627 ng × h/mL
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
GUANADREL plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
3.69 h
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
GUANADREL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
6.8 h
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
GUANADREL plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
Doses

Doses

DosePopulationAdverse events​
150 mg 1 times / day steady, oral
Highest studied dose
Dose: 150 mg, 1 times / day
Route: oral
Route: steady
Dose: 150 mg, 1 times / day
Sources:
unhealthy, 41 years (range: 17 - 68 years)
n = 21
Health Status: unhealthy
Condition: hypertension
Age Group: 41 years (range: 17 - 68 years)
Sex: M+F
Population Size: 21
Sources:
40 mg 1 times / day multiple, oral
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, 54 years (range: 43 - 64 years)
Health Status: unhealthy
Condition: hypertension
Age Group: 54 years (range: 43 - 64 years)
Sex: M+F
Sources:
Disc. AE: Urinary incontinence...
AEs leading to
discontinuation/dose reduction:
Urinary incontinence (1 patient)
Sources:
AEs

AEs

AESignificanceDosePopulation
Urinary incontinence 1 patient
Disc. AE
40 mg 1 times / day multiple, oral
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, 54 years (range: 43 - 64 years)
Health Status: unhealthy
Condition: hypertension
Age Group: 54 years (range: 43 - 64 years)
Sex: M+F
Sources:
PubMed

PubMed

TitleDatePubMed
Comparison of guanadrel and guanethidine efficacy and side effects.
1983
N-hydroxyl derivatives of guanidine based drugs as enzymatic NO donors.
2001 Sep 3
Development of a list of potentially inappropriate drugs for the korean elderly using the delphi method.
2010 Dec
Patents

Sample Use Guides

In Vivo Use Guide
For high blood pressure: Adults—At first, 5 milligrams (mg) two times a day. Then, may be increased up to 20 to 75 mg a day, divided into two to four doses.
Route of Administration: Oral
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:04:16 UTC 2023
Edited
by admin
on Fri Dec 15 15:04:16 UTC 2023
Record UNII
MT147RMO91
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GUANADREL SULFATE
HSDB   MART.   MI   ORANGE BOOK   USAN   USP   VANDF   WHO-DD  
USAN  
Official Name English
GUANIDINE (1,4-DIOXASPIRO(4.5)DEC-2-YLMETHYL)-, SULPHATE (2:1)
Systematic Name English
NSC-760062
Code English
GUANADREL SULFATE [USP IMPURITY]
Common Name English
GUANADREL SULFATE [VANDF]
Common Name English
GUANADREL SULPHATE
Common Name English
CL-1388R
Code English
HYLOREL
Brand Name English
Guanadrel sulfate [WHO-DD]
Common Name English
1,4-DIOXASPIRO(4.5)DEC-2-YLMETHYL)GUANIDINE SULPHATE (2:1)
Common Name English
GUANADREL SULFATE [USAN]
Common Name English
U-28,288D
Code English
GUANADREL SULFATE [ORANGE BOOK]
Common Name English
U-28288D
Code English
GUANIDINE (1,4-DIOXASPIRO(4.5)DEC-2-YLMETHYL)-, SULFATE (2:1)
Systematic Name English
1,4-DIOXASPIRO(4.5)DEC-2-YLMETHYL)GUANIDINE SULFATE (2:1)
Common Name English
GUANADREL SULFATE [MI]
Common Name English
GUANADREL SULFATE [MART.]
Common Name English
GUANADREL SULFATE [HSDB]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C270
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
Code System Code Type Description
EVMPD
SUB02424MIG
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
PRIMARY
CAS
22195-34-2
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
PRIMARY
PUBCHEM
68552
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
PRIMARY
CHEBI
5556
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
PRIMARY
ChEMBL
CHEMBL1037
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
PRIMARY
SMS_ID
100000086695
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
PRIMARY
NCI_THESAURUS
C65828
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
PRIMARY
FDA UNII
MT147RMO91
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
PRIMARY
NSC
760062
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
PRIMARY
HSDB
6536
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
PRIMARY
RXCUI
91239
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID8045432
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
PRIMARY
MERCK INDEX
m5864
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
PRIMARY Merck Index
DRUG BANK
DB00226
Created by admin on Fri Dec 15 15:04:16 UTC 2023 , Edited by admin on Fri Dec 15 15:04:16 UTC 2023
PRIMARY
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ACTIVE MOIETY