UCSF

ZINC00057175

Substance Information

In ZINC since Heavy atoms Benign functionality
October 4th, 2005 15 Yes

Other Names:

1,4-Benzenediamine, 2,6-dichloro-N'-(4,5-dihydro-1H-imidazol-2-yl)-

1,4-Benzenediamine, 2,6-dichloro-N'-(4,5-dihydro-1H-imidazol-2-yl)-; 2-(4-amino-2,6-dichloro)phenyliminoimidazolidine; 4-aminoclonidine; ALO 2145; ALO-2145; Apraclonidina [INN-Spanish]; Apraclonidine [INN:BAN]; Apraclonidinum [INN-Latin]; C9H10Cl2N4; Iopi

1,4-Benzenediamine, 2,6-dichloro-N(sup 1)-(4,5-dihydro-1H-imidazol-2-yl)-, monohydrochloride; 1,4-Benzenediamine, 2,6-dichloro-N(sup 1)-2-imidazolidinylidene-, monohydrochloride; 2,6-Dichloro-N(sup 1)-(2-imidazolidinylidene)-1,4-benzenediamine hydrochlori

2,6-dichloro-1-N-(4,5-dihydro-1H-imidazol-2-yl)benzene-1,4-diamine

2,6-dichloro-N(1)-(4,5-dihydro-1H-imidazol-2-yl)benzene-1,4-diamine

2,6-Dichloro-N1-(4,5-dihydro-1H-imidazol-2-yl)benzene-1,4-diamine

2,6-Dichloro-N1-(4,5-dihydro-1H-imidazol-2-yl)benzene-1,4-diamine hydrochloride

2-(4-amino-2,6-dichloro)phenyliminoimidazolidine

2-(4-Amino-2,6-dichloroanilino)-2-imidazoline hydrochloride

4-Aminoclonidine

4-Aminoclonidine; Apraclonidine

66711-21-5

66711-21-5; Apraclonidine (INN); D07461; Iopidine (TN)

66711-21-5; Apraclonidine; C07668

73218-79-8; Apraclonidine hydrochloride (JAN/USP); D01008; Iopidine (TN)

A0779_SIGMA

AC-12697

AC1L1D6L

AL-02145

ALO 2145

ALO-2145

Aplonidine

Aplonidine hydrochloride

Apraclonidina

Apraclonidina [INN-Spanish]

Apraclonidina [INN-Spanish];Apraclonidinum [INN-Latin]

apraclonidina; apraclonidine; apraclonidinum

Apraclonidine (BAN

Apraclonidine (INN)

APRACLONIDINE HCL

Apraclonidine Hydrochloride

Apraclonidine [INN:BAN]

Apraclonidinum

Apraclonidinum [INN-Latin]

C07668

C9H10Cl2N4

CHEBI:127495

CHEBI:2788

CHEMBL647

CID2216

D07461

DAP000236

DB00964

INN); Apraclonidine HCl (FDA

INN); Apraclonidine Hydrochloride (FDA

Iopidine

Iopidine (TN)

Iopidine Eye

L000686

L013394

LS-176536

MFCD00135922

MFCD00865638

MolPort-003-940-020

MolPort-005-933-986

NCGC00015033-01

NCGC00015033-03

NCGC00162050-01

p-aminoclonidine

P-Aminoclonidine Hydrochloride

para-aminoclonidine

PDSP1_000790

PDSP2_000778

SMP1_000016

UNII-843CEN85DI

USAN

USAN)

USP

USP)

ZINC00020231

Download: MOL2 SDF SMILES Flexibase

Physical Representations

Type pH range xlogP Des A‑Pol Apolar desolvation (kcal/mol) Des Pol Polar desolvation (kcal/mol) H Don H-bond donors H Acc H-bond acceptors Chg Net charge tPSA (Ų) MWT Molecular weight (g/mol) RB Rotatable bonds DL
Ref Reference (pH 7) 1.64 4.03 -24.39 5 4 1 64 246.121 2

Vendor Notes

Note Type Comments Provided By
ALOGPS_SOLUBILITY 4.09e-01 g/l DrugBank-approved
Purity 95% Fluorochem
Purity 98.5% APIChem

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
ADA1A-2-E Alpha-1a Adrenergic Receptor (cluster #2 Of 3), Eukaryotic Eukaryotes 180 0.63 Binding ≤ 10μM
ADA1B-4-E Alpha-1b Adrenergic Receptor (cluster #4 Of 4), Eukaryotic Eukaryotes 180 0.63 Binding ≤ 10μM
ADA1D-2-E Alpha-1d Adrenergic Receptor (cluster #2 Of 3), Eukaryotic Eukaryotes 180 0.63 Binding ≤ 10μM
ADA2A-2-E Alpha-2a Adrenergic Receptor (cluster #2 Of 4), Eukaryotic Eukaryotes 4 0.78 Binding ≤ 10μM
ADA2B-2-E Alpha-2b Adrenergic Receptor (cluster #2 Of 4), Eukaryotic Eukaryotes 5 0.77 Binding ≤ 10μM
ADA2C-2-E Alpha-2c Adrenergic Receptor (cluster #2 Of 4), Eukaryotic Eukaryotes 4 0.78 Binding ≤ 10μM
ADA1A-2-E Alpha-1a Adrenergic Receptor (cluster #2 Of 2), Eukaryotic Eukaryotes 180 0.63 Functional ≤ 10μM
ADA1B-1-E Alpha-1b Adrenergic Receptor (cluster #1 Of 1), Eukaryotic Eukaryotes 180 0.63 Functional ≤ 10μM
ADA1D-4-E Alpha-1d Adrenergic Receptor (cluster #4 Of 4), Eukaryotic Eukaryotes 180 0.63 Functional ≤ 10μM
ADA2A-1-E Alpha-2a Adrenergic Receptor (cluster #1 Of 3), Eukaryotic Eukaryotes 2 0.81 Functional ≤ 10μM
ADA2B-1-E Alpha-2b Adrenergic Receptor (cluster #1 Of 3), Eukaryotic Eukaryotes 2 0.81 Functional ≤ 10μM
ADA2C-1-E Alpha-2c Adrenergic Receptor (cluster #1 Of 3), Eukaryotic Eukaryotes 2 0.81 Functional ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
ADA1A_HUMAN P35348 Alpha-1a Adrenergic Receptor, Human 180 0.63 Binding ≤ 1μM
ADA1B_HUMAN P35368 Alpha-1b Adrenergic Receptor, Human 180 0.63 Binding ≤ 1μM
ADA1D_HUMAN P25100 Alpha-1d Adrenergic Receptor, Human 180 0.63 Binding ≤ 1μM
ADA2A_HUMAN P08913 Alpha-2a Adrenergic Receptor, Human 2.9 0.80 Binding ≤ 1μM
ADA2B_HUMAN P18089 Alpha-2b Adrenergic Receptor, Human 4 0.78 Binding ≤ 1μM
ADA2B_RAT P19328 Alpha-2b Adrenergic Receptor, Rat 4.8 0.78 Binding ≤ 1μM
ADA2C_HUMAN P18825 Alpha-2c Adrenergic Receptor, Human 30 0.70 Binding ≤ 1μM
ADA1A_HUMAN P35348 Alpha-1a Adrenergic Receptor, Human 180 0.63 Binding ≤ 10μM
ADA1B_HUMAN P35368 Alpha-1b Adrenergic Receptor, Human 180 0.63 Binding ≤ 10μM
ADA1D_HUMAN P25100 Alpha-1d Adrenergic Receptor, Human 180 0.63 Binding ≤ 10μM
ADA2A_HUMAN P08913 Alpha-2a Adrenergic Receptor, Human 2.9 0.80 Binding ≤ 10μM
ADA2B_RAT P19328 Alpha-2b Adrenergic Receptor, Rat 4.8 0.78 Binding ≤ 10μM
ADA2B_HUMAN P18089 Alpha-2b Adrenergic Receptor, Human 4 0.78 Binding ≤ 10μM
ADA2C_HUMAN P18825 Alpha-2c Adrenergic Receptor, Human 30 0.70 Binding ≤ 10μM
ADA1A_HUMAN P35348 Alpha-1a Adrenergic Receptor, Human 180 0.63 Functional ≤ 10μM
ADA1B_HUMAN P35368 Alpha-1b Adrenergic Receptor, Human 180 0.63 Functional ≤ 10μM
ADA1D_HUMAN P25100 Alpha-1d Adrenergic Receptor, Human 180 0.63 Functional ≤ 10μM
ADA2A_HUMAN P08913 Alpha-2a Adrenergic Receptor, Human 1.9 0.81 Functional ≤ 10μM
ADA2B_HUMAN P18089 Alpha-2b Adrenergic Receptor, Human 1.9 0.81 Functional ≤ 10μM
ADA2C_HUMAN P18825 Alpha-2c Adrenergic Receptor, Human 1.9 0.81 Functional ≤ 10μM

Reactome Annotations from Targets (via Uniprot)

Description Species
Adrenaline signalling through Alpha-2 adrenergic receptor
Adrenaline,noradrenaline inhibits insulin secretion
Adrenoceptors
G alpha (12/13) signalling events
G alpha (i) signalling events
G alpha (q) signalling events
G alpha (z) signalling events

Analogs ( Draw Identity 99% 90% 80% 70% )