UCSF

ZINC03872277

Substance Information

In ZINC since Heavy atoms Benign functionality
October 4th, 2005 14 Yes

CAS Numbers: 364-98-7 , [364-98-7]

Other Names:

2H-1,2, 4-Benzothiadiazine, 7-chloro-3-methyl-, 1,1-dioxide

2H-1,2,4-Benzothiadiazine, 7-chloro-3-methyl-, 1,1-dioxide

2H-1,2,4-Benzothiadiazine, 7-chloro-3-methyl-, 1,1-dioxide; 7-Chloro-3-methyl-2H-1,2,4-benzothiadiazine 1,1-dioxide; 7-Cloro-3-metil-2H-1,2,4-benzotiodiazina-1,1-diossido [Italian]; C8H7ClN2O2S; DIAZOXIDE; Diazossido [DCIT]; Diazossido [Italian]; Diazoxid

364-98-7

364-98-7; C06949; Diazoxide

364-98-7; D00294; Diazoxide (JAN/USP/INN); Hyperstat (TN)

364-98-7; Diazoxide; Prestwick_163

7-Chloro-3-methyl-1lambda~4~,2,4-benzothiadiazin-1-ol 1-oxide

7-chloro-3-methyl-2H-1$l^{6},2,4-benzothiadiazine-1,1-dione

7-Chloro-3-methyl-2H-1,2,4-benzothiadiazine 1,1-dioxide

7-chloro-3-methyl-4H-1

7-Cloro-3-metil-2H-1,2,4-benzotiodiazina-1,1-diossido

7-Cloro-3-metil-2H-1,2,4-benzotiodiazina-1,1-diossido [Italian]

AC1L1EZN

Aroglycem

Bio1_000036

Bio1_000525

Bio1_001014

Bio2_000027

Bio2_000507

BPBio1_000016

BRD-K73109821-001-05-2

BSPBio_000014

BSPBio_001307

BSPBio_002290

C06949

C8H7ClN2O2S

CAS-364-98-7

CBiol_001750

CHEBI:4495

CHEBI:6046

CHEMBL181

CID3019

CPD000058392

CPD000058392; DIAZOXIDE

CPD000058392; DIAZOXIDE; SAM001246872

D 9035

D00294

D003981

D9035_SIGMA

DAP000956

DB01119

Diazossido

Diazossido [DCIT]

Diazossido [Italian]

Diazossido; Diazoxide

Diazoxide (BAN

Diazoxide (JAN/USP/INN)

Diazoxide [USAN:INN:BAN]

diazoxide; diazoxido; diazoxidum

Diazoxido

Diazoxido [INN-Spanish]

Diazoxidum

Diazoxidum [INN-Latin]

Dizoxide

EINECS 206-668-1

EU-0100404

Eudemine

Eudimine

FDA

HMS1361B09

HMS1568A16

HMS1791B09

HMS1922L22

HMS1989B09

HMS2051P20

HMS2089L04

HMS2093N12

Hyperstat

Hyperstat (TN)

Hypertonalum

I06-2041

IDI1_033777

INN

KBio2_000027

KBio2_002595

KBio2_005163

KBio3_000053

KBio3_000054

KBio3_001510

KBioGR_000027

KBioGR_001776

KBioSS_000027

LS-40410

MFCD00078578

MLS000028459

MLS001076071

MolPort-003-666-772

MolPort-003-941-186

Mutabase

NCGC00015380-01

NCGC00015380-02

NCGC00015380-03

NCGC00015380-05

NCGC00015380-12

NCGC00024907-01

NCGC00024907-02

NCGC00024907-03

NCGC00024907-04

NCGC00024907-05

NCGC00024907-06

NCGC00024907-07

NCGC00024907-08

nchembio.150-comp49

nchembio.476-comp10

NSC 64198

NSC 76130

NSC-64198

NSC64198

NSC76130

Prestwick0_000087

Prestwick1_000087

Prestwick2_000087

Prestwick3_000087

Prestwick_163

Proglicem

Proglycem

SAM001246872

Sch 6783

SCH-6783

SCH-6783; SRG-95213

SMR000058392

SPBio_001953

SPECTRUM2300206

Spectrum3_000735

Spectrum4_001248

SRG 95213

SRG-95213

Tocris-0964

UNII-O5CB12L4FN

USAN

USP)

VU0239714-6

ZINC03872277

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) 1.84 2.16 -20.72 1 4 0 59 230.676 0
Hi High (pH 8-9.5) 1.84 1.75 -35.07 0 4 -1 61 229.668 0

Vendor Notes

Note Type Comments Provided By
ALOGPS_SOLUBILITY 5.52e-01 g/l DrugBank-approved
purity 9.500000000000000e+001 Enamine Building Blocks Enamine Building Blocks
Purity 99% Fluorochem
Therapy Activator of ATP-dependent K+ channels in both vascular smooth muscle and pancreatic beta-cells; antihypertensive SMDC Iconix
therap antihypertensive, diuretic, activates K channels and AMPA receptors MicroSource Spectrum
PUBCHEM_SUBSTANCE_COMMENT NCC_SAMPLE_SUPPLIER : Sigma Chemical Company; NCC_SUPPLIER_STRUCTURE_ID : D9035 NIH Clinical Collection via PubChem
PUBCHEM_SUBSTANCE_COMMENT SAMPLE_SUPPLIER: Sigma Chemical Company; SUPPLIER_STRUCTURE_ID: D9035 NIH Clinical Collection via PubChem

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
ABCC8-1-E Sulfonylurea Receptor 1 (cluster #1 Of 1), Eukaryotic Eukaryotes 8800 0.51 Functional ≤ 10μM
IRK11-1-E Potassium Channel, Inwardly Rectifying, Subfamily J, Member 11 (cluster #1 Of 1), Eukaryotic Eukaryotes 8800 0.51 Functional ≤ 10μM
Z50597-1-O Rattus Norvegicus (cluster #1 Of 12), Other Other 6100 0.52 Functional ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
IRK11_HUMAN Q14654 Potassium Channel, Inwardly Rectifying, Subfamily J, Member 11, Human 8800 0.51 Functional ≤ 10μM
Z50597 Z50597 Rattus Norvegicus 6100 0.52 Functional ≤ 10μM
ABCC8_HUMAN Q09428 Sulfonylurea Receptor 1, Human 8800 0.51 Functional ≤ 10μM

Reactome Annotations from Targets (via Uniprot)

Description Species
ABC-family proteins mediated transport
ATP sensitive Potassium channels
Regulation of insulin secretion

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