Small Molecule dopamine

URN urn:agi-cas:51-61-6
Total Entities 0
Connectivity 3850
Name dopamine

Pathway Gap Junction Assembly
Young Onset SNCA Induced Parkinson's Disease
Dopamine Metabolism in Parkinson's Disease
Neurotoxin-Induced Parkinson's Disease
Metals and Amyloid beta Toxicity
Overt Hypothyroidism Influence on Thyroid-Stimulating Hormone Secretion
Central Hypothyroidism Overview
Tertiary Hypothyroidism Overview
Induction of Apoptosis and Immediate Early Gene Activation in Hippocampal Neurons Following Seizures
Phenylalanine and Tyrosine metabolism
CNR1/2 -> membrane transport
DRD2 -> TRPC1 transcription
DRD1/3 -> potassium uptake
DRD2/4 -> membrane transport
DRD3 -> dopamine uptake
Nociception-related DRD2 expression targets
Nociception-related DRD1/5 expression targets
CCKBR -> neurotransmitter uptake
TAAR1 -> neurotransmitter uptake
Epinephrine/Norepinephrine release cycle
Dopamine release cycle
Regulation of potassium flux
Summarized nociception-related expression targets
Regulation of calcium flux
DopamineR2 -> AP-1/CREB/ELK-SRF signaling
DopamineR2 -> NF-kB signaling
DopamineR1 -> CREB/ELK-SRF signaling
Dopamine/Gi Expression Targets
Dopamine/Gs Expression Targets
dopamine signaling pathway
peripheral dopamine signaling pathway
acetylcholine signaling pathway via nicotinic acetylcholine receptor
epinephrine biosynthetic pathway
norepinephrine biosynthetic pathway
dopamine signaling pathway
norepinephrine biosynthetic pathway
epinephrine biosynthetic pathway
norepinephrine biosynthetic pathway
dopamine biosynthetic pathway
epinephrine biosynthetic pathway

Group Biofluids assayable substances

Source ChemIDplus

Alias 3-hydroxytyramine hydrobromide
62-31-7
KW-3-060
dopamin guilini
dopamin braun
dopamin awd
dopamex
docard
catabon
cardiosteril
cardiopal
3 hydroxy tyramine
dopamin natterman
Uramin
dopamine hydrochloride and dextrose 5%
51-61-6
50444-17-2
1477-71-0
Revivan
P498 cpd
P-498
P 498
Oxytyramine
NSC 173182
NSC 169105
m-Hydroxytyramine hydrochloride
Intropin
3-Hydroxtyramine
levodopamine
levo dopamine
l dopamine
intropin iv
inovan
inotropin
inopin
inopan
giludop
dynos
dopamin leopold
dopmin e
4-(2-Aminoethyl)pyrocatechol HCl
[(18)F]dopamine
asl 279
[G-3H]Dopamine
(G-3H)Dopamine
tensamin
beta-(3,4-Dihydroxyphenyl)ethylamine HCl
3,4-Dihydroxyphenethylamine HCl
dopmin
dopinga
dopaminex
dopamine hydrochloride in dextrose 5%
drynalken
2-(3,4-Dihydroxyphenyl)ethylamine
4-(2-Aminoethyl)pyrocatechol
4-(2-Aminoethyl)catechol
4-(2-aminoethyl)benzene-1,2-diol
4-(2-Aminoethyl)-1,2-bezenediol
[11C]dopamine
[14C]dopamine
[1S-3H]dopamine
[2,2-2H2]dopamine
[2S-3H]dopamine
m-Hydroxytyramine HCl
4-(2-Aminoethyl)pyrocatechol hydrochloride
[7-14C]dopamine
[2H2]-dopamine
3,4 Dihydroxyphenethylamine
3,4-Dihydroxyphenethylamine hydrochloride
3,4-Dihydroxyphenylethylamine
4-(2-aminoethyl)-1,2-Benzenediol labeled with tritium
4-(2-Aminoethyl)-1,2-benzenediol
3-hydroxytyramine-HCl
3-Hydroxytyramine hydrochloride
3-Hydroxytyramine
3H-ADTN
3,4-dihydroxyphenyl-ethylamine
Hydroxytyramine
[3H]dopamine
Dynatra
Hydroxytyramin
HSDB 3068
[3H]3,4-dihydroxyphenylethylamine
EINECS 200-110-0
4-(aminoethyl)catechol
Dophamine
Dopastat
Dopaminum
dopamines
dopamine-3H
dopamine-14C
dopamine-1
Dopamine hydrochloride
D2-dopamine
EINECS 200-527-8
dopamine concentrate sterile
a-(3,4-Dihydroxyphenyl)-b-aminoethane
beta-(3,4-Dihydroxyphenyl)ethylamine hydrochloride
dihydroxyphenylethylamine
dipropyl DA
Dopamin
Dopamina
4-dihydroxyphenylethylamine
dopamine
Dopamine chloride
alpha-(3,4-Dihydroxyphenyl)-beta-aminoethane
ASL-279
up 3,4-dihydroxyphenylethylamine

KEGG ID C03758

MedScan ID 1003345

HMDB ID HMDB00073

PharmaPendium Name Dopamine Hydrochloride

CAS ID 51-61-6
1477-71-0
62-31-7
50444-17-2

PubChem SID 134972588
135022549
135124979
148617
207316
748365

PubChem CID 681
65340

IUPAC Name 4-(2-aminoethyl)pyrocatechol
4-(2-aminoethyl)pyrocatechol;hydrochloride
4-(2-aminoethyl)pyrocatechol hydrochloride

InChIKey VYFYYTLLBUKUHU-UHFFFAOYSA-N
CTENFNNZBMHDDG-UHFFFAOYSA-N

Rotatable Bond Count 2

Molecular Weight 153.178440
189.639380
153.178440
189.639380
153.178440
189.639380
153.178440
189.639380

Molecular Formula C8H11NO2
C8H12ClNO2

XLogP -1.000000
-1.000000

ChEBI ID 18243

Reaxys ID 1072822
4134622
5529929
8136385

LinkUrl http://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=CHEBI:18243&species=All