Page last updated: 2024-09-21

carbamylhydrazine monohydrochloride

Cross-References

ID SourceID
PubMed CID11236
CHEMBL ID1256355
CHEBI ID82532
SCHEMBL ID6932
MeSH IDM0311029

Synonyms (88)

Synonym
34854vg84b ,
hydrazinecarboxamide, hydrochloride (1:1)
unii-34854vg84b
AKOS015848282
hydrazinecarboxamide hydrochloride
carbamyl hydrazine.hcl
hydrazinecarboxamide, monohydrochloride
nsc4732
semicarbazide monohydrochloride
amidourea hydrochloride
563-41-7
carbamylhydrazine hydrochloride
ek 226
aminourea hydrochloride
wln: zvmz &gh
semicarbazide hydrochloride
hydrazinecarboxamide, hydrochloride
semicarbazide chloride
semicarbazide, monohydrochloride
hydrazinecarboxamide monohydrochloride
semicarbazide hcl
nsc-4732
semicarbazide, hydrochloride
EU-0101096
semicarbazide hydrochloride, >=99%
NCGC00091589-01
semicarbazide hydrochloride (van)
einecs 209-247-0
nsc 4732
ccris 556
hsdb 5197
ai3-52680
hydrazinecarboxamide, hydrochloride (van)
NCGC00094369-01
S-2460
MLS002153236
smr000326716
hydrazine carboxamide hydrochloride
S 2201
C19521
CHEMBL1256355
chebi:82532 ,
NCGC00258503-01
tox21_200950
dtxcid20244
cas-563-41-7
dtxsid4020244 ,
semikarbazide hydrochloride
ch6cln3o
n-aminoureahydrochloride
FT-0674553
873205-62-0
FT-0632395
LP01096
semicarbazide hydrochloride [mi]
semicarbazide hydrochloride [hsdb]
semicarbazide hydrochloride [iarc]
CCG-222400
SCHEMBL6932
tox21_501096
NCGC00261781-01
hydrazinecarbox-amide hydrochloride
nh2nhconh2.hcl
semicarbazide-hydrochloride
XHQYBDSXTDXSHY-UHFFFAOYSA-N
semicarbazide hydrocloride
semicarbazide hcl salt
hydrochloric acid semicarbazide
semi-carbazide hydrochloride
semicarbazide.hydrochloride
mfcd00013009
F1908-0069
semicarbazide hydrochloride, purum p.a., >=98.0% (at)
semicarbazide hydrochloride, vetranal(tm), analytical standard
semicarbazide hydrochloride, saj special grade, >=99.0%
semicarbazide hydrochloride, p.a., 99.0%
SR-01000075648-2
sr-01000075648
CS-W018530
semicarbazide (hydrochloride)
Q27156046
STR00205
D77852
HY-Y0470
hydrazinecarboxamidehydrochloride
aminourea;hydrochloride
EN300-19461
Z104473922

Drug Classes (1)

ClassDescription
organic molecular entityAny molecular entity that contains carbon.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Protein Targets (18)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, MAJOR APURINIC/APYRIMIDINIC ENDONUCLEASEHomo sapiens (human)Potency26.67950.003245.467312,589.2998AID2517
Chain A, JmjC domain-containing histone demethylation protein 3AHomo sapiens (human)Potency89.12510.631035.7641100.0000AID504339
endonuclease IVEscherichia coliPotency4.46680.707912.432431.6228AID1708
thioredoxin reductaseRattus norvegicus (Norway rat)Potency10.62130.100020.879379.4328AID588453
RAR-related orphan receptor gammaMus musculus (house mouse)Potency0.00500.006038.004119,952.5996AID1159521
GLI family zinc finger 3Homo sapiens (human)Potency72.34890.000714.592883.7951AID1259369; AID1259392
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency63.17150.000214.376460.0339AID720692
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency67.71990.003041.611522,387.1992AID1159552; AID1159553; AID1159555
pregnane X nuclear receptorHomo sapiens (human)Potency19.80390.005428.02631,258.9301AID1346982
estrogen nuclear receptor alphaHomo sapiens (human)Potency5.63020.000229.305416,493.5996AID743075
IDH1Homo sapiens (human)Potency3.26430.005210.865235.4813AID686970
euchromatic histone-lysine N-methyltransferase 2Homo sapiens (human)Potency0.02240.035520.977089.1251AID504332
chromobox protein homolog 1Homo sapiens (human)Potency89.12510.006026.168889.1251AID540317
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency47.30790.000627.21521,122.0200AID651741
DNA polymerase eta isoform 1Homo sapiens (human)Potency89.12510.100028.9256213.3130AID588591
DNA polymerase iota isoform a (long)Homo sapiens (human)Potency89.12510.050127.073689.1251AID588590
gemininHomo sapiens (human)Potency0.16360.004611.374133.4983AID624297
lamin isoform A-delta10Homo sapiens (human)Potency5.62340.891312.067628.1838AID1487
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (16)

Assay IDTitleYearJournalArticle
AID504812Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID651635Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression
AID1745845Primary qHTS for Inhibitors of ATXN expression
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID504810Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID521220Inhibition of neurosphere proliferation of mouse neural precursor cells by MTT assay2007Nature chemical biology, May, Volume: 3, Issue:5
Chemical genetics reveals a complex functional ground state of neural stem cells.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).2014Journal of biomolecular screening, Jul, Volume: 19, Issue:6
A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (25.00)29.6817
2010's4 (50.00)24.3611
2020's2 (25.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other8 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]