noradrenaline
SMILES | NCC(c1ccc(c(c1)O)O)O |
InChIKey | SFLSHLFXELFNJZ-UHFFFAOYSA-N |
Chemical properties
Hydrogen bond acceptors | 4 |
Hydrogen bond donors | 4 |
Rotatable bonds | 2 |
Molecular weight (Da) | 169.1 |
Drug properties
Molecular type | Small molecule |
Physiological/Surrogate | Endogenous |
Approved drug | No |
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
β1 | ADRB1 | Human | Adrenoceptors | A | pKi | 6.0 | 6.0 | 6.0 | Guide to Pharmacology |
β2 | ADRB2 | Human | Adrenoceptors | A | pKi | 5.4 | 5.4 | 5.4 | Guide to Pharmacology |
D1 | DRD1 | Human | Dopamine | A | pKi | 4.3 | 4.3 | 4.3 | Guide to Pharmacology |
D5 | DRD5 | Human | Dopamine | A | pKi | 4.9 | 4.9 | 4.9 | Guide to Pharmacology |
D1 | DRD1 | Human | Dopamine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
D2 | DRD2 | Human | Dopamine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
5-HT1A | 5HT1A | Human | 5-Hydroxytryptamine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
5-HT2A | 5HT2A | Rat | 5-Hydroxytryptamine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
5-HT5A | 5HT5A | Rat | 5-Hydroxytryptamine | A | pKi | 5.0 | 5.5 | 6.0 | PDSP Ki database |
5-HT2A | 5HT2A | Bovine | 5-Hydroxytryptamine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
5-HT2C | 5HT2C | Rat | 5-Hydroxytryptamine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
α1B | ADA1B | Human | Adrenoceptors | A | pKi | 5.0 | 5.39 | 6.04 | PDSP Ki database |
α1D | ADA1D | Rat | Adrenoceptors | A | pKi | 7.0 | 7.0 | 7.0 | PDSP Ki database |
α1B | ADA1B | Rat | Adrenoceptors | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
5-HT7 | 5HT7R | Human | 5-Hydroxytryptamine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
5-HT5A | 5HT5A | Mouse | 5-Hydroxytryptamine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
5-HT6 | 5HT6R | Mouse | 5-Hydroxytryptamine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
α2A | ADA2A | Pig | Adrenoceptors | A | pKi | 5.25 | 5.84 | 6.43 | PDSP Ki database |
5-HT1B | 5HT1B | Rat | 5-Hydroxytryptamine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
β2 | ADRB2 | Human | Adrenoceptors | A | pKi | 5.0 | 5.27 | 6.1 | PDSP Ki database |
D1 | DRD1 | Rat | Dopamine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
D2 | DRD2 | Rat | Dopamine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
5-HT1A | 5HT1A | Rat | 5-Hydroxytryptamine | A | pKi | 5.0 | 5.42 | 6.26 | PDSP Ki database |
5-HT7 | 5HT7R | Rat | 5-Hydroxytryptamine | A | pKi | 6.0 | 6.09 | 6.26 | PDSP Ki database |
D5 | DRD5 | Human | Dopamine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
α2A | ADA2A | Human | Adrenoceptors | A | pKi | 5.7 | 6.03 | 6.4 | PDSP Ki database |
TA1 | TAAR1 | Human | Trace amine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
α1A | Q9TSW7 | Pig | Adrenoceptors | A | pKi | 5.0 | 5.12 | 5.3 | PDSP Ki database |
α1D | ADA1D | Human | Adrenoceptors | A | pKi | 5.0 | 5.03 | 5.06 | PDSP Ki database |
D1 | DRD1 | Bovine | Dopamine | A | pKi | 6.09 | 6.39 | 6.7 | PDSP Ki database |
α2B | ADA2B | Human | Adrenoceptors | A | pKi | 5.56 | 6.02 | 6.48 | PDSP Ki database |
α2C | ADA2C | Human | Adrenoceptors | A | pKi | 5.87 | 6.05 | 6.23 | PDSP Ki database |
D2 | DRD2 | Dog | Dopamine | A | pKi | 5.22 | 5.22 | 5.22 | PDSP Ki database |
β1 | ADRB1 | Human | Adrenoceptors | A | pKi | 5.45 | 5.45 | 5.45 | PDSP Ki database |
β3 | ADRB3 | Human | Adrenoceptors | A | pKi | 5.37 | 5.37 | 5.37 | PDSP Ki database |
α2A | ADA2A | Mouse | Adrenoceptors | A | pKi | 5.85 | 5.85 | 5.85 | PDSP Ki database |
CB1 | CNR1 | Human | Cannabinoid | A | pKi | 6.0 | 6.0 | 6.0 | PDSP Ki database |
5-HT2A | 5HT2A | Human | 5-Hydroxytryptamine | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
D2 | DRD2 | Bovine | Dopamine | A | pKi | 5.0 | 5.12 | 5.25 | PDSP Ki database |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
TA1 | TAAR1 | Human | Trace amine | A | pEC50 | 4.91 | 4.91 | 4.91 | ChEMBL |