Cinchocaine 1.1% ointment
A local anesthetic of the amide type now generally used for surface anesthesia.
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Suspected adverse reactions reported for Cinchocaine
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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Suspected adverse reactions reported for Cinchocaine
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1 branded products available
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(1)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
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Codes for healthcare professionals and prescribing systems
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NHS UK identifiers
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Randomised trials: 2 · 1963–2025
Showing the 50 most relevant studies, sorted by most relevant.
P. T. Cook, Melanie J. Davies, Keith D. Cronin, et al.
Anaesthesia and Intensive Care, 1986
- Dibucaine
- Anesthesia, Spinal
- Anesthesia, General
Rabab Mohamed Mohamed, Mohamed Abdelbadie, Attia Gad Anwar
Anaesthesia, Pain & Intensive Care, 2025
Background & Objectives: Transurethral resection of the prostate (TURP) is commonly performed under spinal anesthesia. The advent of bupivacaine replaced cinchocaine, hyperbaric bupivacaine became the favorite, as it offered prolonged effect and maneuverability of the position of the patient. The objective of this research was to assess the efficacy of three distinct concentrations of intrathecal dexmedetomidine in conjunction with 0.5% hyperbaric bupivacaine in TURP. Methods: This randomized, double-blind study included ninety patients aged 55 to 70 yr admitted for TURP. Patients were divided into three groups; Group A received 1.5 mL hyperbaric bupivacaine 0.5% plus 6 µg dexmedetomidine, Group B received 1.5 mL hyperbaric bupivacaine 0.5% plus 8 µg dexmedetomidine and Group C was administered 1.5 mL hyperbaric bupivacaine 0.5% plus 10 µg dexmedetomidine. The time to onset and duration of sensory and motor block were noted. Postoperatively, morphine was used for analgesia and time to first dose and the total consumption of morphine was noted in each patient. Pain was assessed at NRS scores at 6, 8, and 12 h. Results: An absence of statistically significant variation was noted at the onset and duration of sensory block and motor block between Groups A and B. Nevertheless, when comparing Group C to Groups A and B, the time to onset was considerably reduced (P < 0.05). The duration of first rescue analgesic was significantly prolonged in Groups C and B than in Group A, and in Group C than in Group B (P < 0.05). Postoperative total morphine consumption and NRS scores at 6, 8, and 12h were significantly reduced in Groups C and B compared to Group A; and in Group C than Group B (P < 0.05). Conclusions: Combined with hyperbaric bupivacaine, 10 µg of dexmedetomidine significantly prolongs analgesia duration, sensory block, and motor blockade in TURP, as compared to using dexmedetomidine in 6 µg or 8 µg with hyperbaric bupivacaine. This results in a reduction in the requirement of postoperative analgesics, but the incidence of adverse effects is comparable to the lower dosage regimens. Abbreviations: MAP: mean arterial pressure, NRS: Numeric Rating Scale, PACU: post-anesthesia care unit, SA: spinal anesthesia, TURP: Transurethral resection of the prostate. Keywords: Dose; Dexmedetomidine; Hyperbaric Bupivacaine; Pain; Spinal Anesthesia; Sensory Block; Transurethral Resection of the Prostate Citation: Mohamed RM, Abdelbadie M, Anwar AG. Low dose hyperbaric bupivacaine 0.5% with three different doses of dexmedetomidine for spinal anesthesia in transurethral resection of the prostate: A randomized, double-blind trial. Anaesth. pain intensive care 2025;29(3):384-391. DOI: 10.35975/apic.v29i3.2750 Received: May 22, 2024; Revised: January 26, 2025; Accepted: January 26, 2025
Abstract licence: CC BY-NC
David N. Brindley, M Bowley
Biochemical Journal, 1975
- Pharmacology
- Amphetamine
- Chlorpromazine
Mamdouh R. Rezk, Ahmed S. Fayed, Hoda M. Marzouk, et al.
Journal of The Electrochemical Society, 2017
Lynne Jones, Robert H. Michell
Biochemical Journal, 1975
- Calcimycin
- Acetylcholine
- Calcium
Oxford University Press eBooks, 2023
Aminul Islam, Anika Zafreen, Sadia Islam, et al.
Asian Journal of Chemical Sciences, 2025
Jinshan Che, Mingming Sun, Zhipan Li
Reviews in Analytical Chemistry, 2025
Abstract An electrochemical sensor for cinchocaine (CIN) detection was developed based on surface molecular imprinting technology utilizing screen-printed gold electrodes modified with TiO2 nanoparticles and electropolymerized polypyrrole. A novel sensor was developed using a dual-stage methodology, which entailed initial CIN template immobilization and subsequent electrochemical pyrrole polymerization incorporating titanium dioxide nanoscale particles. The sensor exhibited enhanced electroactive surface area (0.075 cm2) and improved electron transfer kinetics (heterogeneous rate constant 8.2 × 10−3 cm·s−1) compared to unmodified electrodes. Under optimized conditions (pH 5.0, 15-min incubation), the sensor demonstrated two linear response ranges from 0.1–10 and 10–100 μM, with a detection limit of 0.035 μM. The sensor showed excellent selectivity against common interferents, including a 100-fold excess of inorganic ions and a 50-fold excess of structurally similar compounds. Analysis of clinical samples yielded excellent recoveries (97.2–102.3%) with relative standard deviations below 4.3%. The simple fabrication process, rapid response time, and minimal sample preparation requirements make this sensor particularly suitable for point-of-care applications.
Abstract licence: CC BY 4.0
Inês C. Farinha, Francisca Cunha Tavares, E. Faria, et al.
Arquivos de Asmas Alergia e Imunologia, 2024
R G Sturton, David N. Brindley
Biochemical Journal, 1977
- Chlorpromazine
- Cytidine Diphosphate Diglycerides
- Edetic Acid
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
1 found
Half-life
Not available
Mechanism
Local anesthetics block both the initiation and conduction of nerve impulses by…
Food interactions
None known
Human targets
3 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
Metabolism
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 1798 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
Proteins and enzymes this drug interacts with in the body
The influx of Na(+) ions provokes membrane depolarization, initiating the propagation of electrical signals throughout cells and tissues .
PMID:1309946 PMID:21447824 PMID:23085483 PMID:23420830 PMID:25370050 PMID:26279430 PMID:26392562 PMID:26776555
Nav1.5 is the predominant sodium channel expressed in myocardial cells and it is responsible for the initial upstroke of the action potential in cardiac myocytes, thereby initiating the heartbeat .
PMID:11234013 PMID:11804990 PMID:12569159 PMID:1309946
Required for normal electrical conduction including formation of the infranodal ventricular conduction system and normal action potential configuration, as a result of its interaction with XIRP2 (By similarity)
PMID:16760425 PMID:31454269
Calcium-binding is required for the activation of calmodulin .
PMID:16760425 PMID:31454269 PMID:35568036
Among the enzymes to be stimulated by the calmodulin-calcium complex are a number of protein kinases, such as myosin light-chain kinases and calmodulin-dependent protein kinase type II (CaMK2), and phosphatases .
PMID:16760425 PMID:35568036
Together with CCP110 and centrin, is involved in a genetic pathway that regulates the centrosome cycle and progression through cytokinesis PMID:16760425
Enzymes involved in drug metabolism — important for understanding drug interactions
ATC D04AB02
ATC S01HA06
ATC S02DA04
ATC N01BB06
ATC C05AD04
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Cinchocaine
Additional database identifiers
Drugs Product Database (DPD)
9206
Drugs Product Database (DPD)
7053
ChemSpider
2917
BindingDB
48532
ZINC
ZINC000001530939
HUGO Gene Nomenclature Committee (HGNC)
HGNC:10593
GenAtlas
SCN5A
GeneCards
SCN5A
GenBank Gene Database
M77235
GenBank Protein Database
184039
Guide to Pharmacology
582
UniProt Accession
SCN5A_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:10582
GenAtlas
SCN10A
GeneCards
SCN10A
GenBank Gene Database
AF117907
GenBank Protein Database
4838145
Guide to Pharmacology
585
UniProt Accession
SCNAA_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1442
GeneCards
CALM1
UniProt Accession
CALM1_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1445
GeneCards
CALM2
UniProt Accession
CALM2_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1449
GeneCards
CALM3
UniProt Accession
CALM3_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:983
GenAtlas
BCHE
GeneCards
BCHE
GenBank Gene Database
M32391
GenBank Protein Database
1311630
Guide to Pharmacology
2471
UniProt Accession
CHLE_HUMAN
DrugBank citations
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Structured knowledge from the free knowledge base
Linked open data from Wikidata (Q417603), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication. WHO INN from the World Health Organization.