Compound Summary

  Compound Information
 niclosamide

Compound Name:

niclosamide

Compound CID:

4477

Synonyms:

niclosamide

50-65-7

5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide

Niclocide

Bayluscid

More...

Iupac Name:

5-chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide

InChI:

InChI=1S/C13H8Cl2N2O4/c14-7-1-4-12(18)9(5-7)13(19)16-11-3-2-8(17(20)21)6-10(11)15/h1-6,18H,(H,16,19)

InChIKey:

RJMUSRYZPJIFPJ-UHFFFAOYSA-N

Canonical Smiles:

C1=CC(=C(C=C1[N+](=O)[O-])Cl)NC(=O)C2=C(C=CC(=C2)Cl)O

Isomeric Smiles:

C1=CC(=C(C=C1[N+](=O)[O-])Cl)NC(=O)C2=C(C=CC(=C2)Cl)O

Molecular Weight:

327.12

Molecular Formula:

C13H8Cl2N2O4

  Compound Structure
 2D Structure:
 3D Structure:
  Computed Properties
 niclosamide

Molecular Weight:

327.12

Molecular Formula:

C13H8Cl2N2O4

Hydrogen Bond Donor Count:

2

Hydrogen Bond Acceptor Count:

4

Rotatable Bond Count:

2

Heavy Atom Count:

21

Complexity:

404

  Synonyms
 niclosamide

niclosamide niclosamide

niclosamide

50-65-7

5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide

Niclocide

Bayluscid

Phenasal

Tredemine

Fenasal

Yomesan

Dichlosale

Helmiantin

Atenase

Cestocid

Devermin

Devermine

Iomesan

Iomezan

Mansonil

Radeverm

Sagimid

Vermitid

Lintex

Nasemo

Sulqui

2,5-Dichloro-4-nitrosalicylanilide

Mato

Fedal-Telmin

Bayer 73

Zestocarp

Bayer 2353

BAY 2353

Benzamide, 5-chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxy-

Chemagro 2353

C13H8Cl2N2O4

5-Chloro-2-chloro-4-nitrosalicylanilide

nicolsamide

HL 2447

WR 46234

Salicylanilide, 2,5-dichloro-4-nitro-

UNII-8KK8CQ2K8G

ENT 25823

2-Hydroxy-5-chloro-N-(2-chloro-4-nitrophenyl)benzamide

N-(2-Chloro-4-nitrophenyl)-5-chlorosalicylamide

2-Chloro-4-nitrophenylamide-6-chlorosalicylic acid

2,5-Dichlor-4-nitro-salizylsaeureanilid"

5-Chloro-N-(2-chloro-4-nitrophenyl)salicylamide

8KK8CQ2K8G

SR 73

Radewerm

N-(2-Chlor-4-nitrophenyl)-5-chlorsalicylamid

MFCD00057597

Niclosamide Anhydrous

NSC-178296

CAS-50-65-7

NCGC00015735-07

DSSTox_CID_20362

DSSTox_RID_79485

DSSTox_GSID_40362

N-(2-Chloro-4-nitrophenyl)-5-chlorosalicylamide

Niclosamida

Niclosamidum

Cestocide

Niclosamidum INN-Latin

Niclosamida INN-Spanish

Nitrophenyl chlorsalicylamide

Niclosamide USAN:INN:BAN

CCRIS 3437

HSDB 1572

SR-01000076024

Niclosamide BSI:ISO

EINECS 200-056-8

NSC 178296

BRN 2820605

Yomensan

AI3-25823

5-Chlorosalicyloyl-(o-chloro-p-nitranilide)

B 2353

Niclocide (TN)

Prestwick_354

2,5-Dichlor-4-nitro-salizylsaeureanilid German

Mollutox (Salt/Mix)

N-(2-Chlor-4-nitrophenyl)-5-chlorsalicylamid German

Spectrum_000239

Niclosamide (Niclocide)

Clonitralid (Salt/Mix)

Clonitralide (Salt/Mix)

Prestwick0_000040

Prestwick1_000040

Prestwick2_000040

Prestwick3_000040

Spectrum2_001183

Spectrum3_000667

Spectrum4_000196

Spectrum5_001083

Lopac-N-3510

Niclosamide (USAN/INN)

CHEMBL1448

Lopac0_000866

Oprea1_259151

SCHEMBL67182

BSPBio_000139

BSPBio_002333

KBioGR_000771

KBioSS_000719

MLS002154181

DivK1c_000709

SPECTRUM1503265

SPBio_001225

SPBio_002060

BPBio1_000153

CHEBI:7553

GTPL8494

DTXSID7040362

SCHEMBL18563900

WLN: WNR CG DMVR BQ EG

BDBM11242

HMS502D11

KBio1_000709

KBio2_000719

KBio2_003287

KBio2_005855

KBio3_001553

5-Chloro-N-(2-chloro-4-nitro-phenyl)-2-hydroxy-benzamide

Niclosamide - CAS 50-65-7

NINDS_000709

HMS1568G21

HMS2093A21

HMS2095G21

HMS2231H06

HMS3262N13

HMS3373P08

HMS3712G21

KUC107299N

Pharmakon1600-01503265

BAY-2353

BCP22958

HY-B0497

ZINC3874496

Tox21_110209

Tox21_300749

Tox21_500866

BBL004110

CCG-39641

NSC178296

NSC758440

s3030

Salicylanilide,5-dichloro-4-nitro-

STK396676

2,5-dichloro-4-nitrosalicylanilide ?

AKOS003589004

Tox21_110209_1

AT15436

BCP9000068

DB06803

KS-5210

LP00866

MCULE-9985514311

NSC-758440

SB19414

SDCCGSBI-0050841.P004

2,5-Dichloro-4-nitrosalicylanilide

IDI1_000709

SMP2_000228

5-chloro-N-(2-chloro-4-nitrophenyl)-

NCGC00015735-01

NCGC00015735-02

NCGC00015735-03

NCGC00015735-04

NCGC00015735-05

NCGC00015735-06

NCGC00015735-08

NCGC00015735-09

NCGC00015735-11

NCGC00015735-12

NCGC00015735-24

NCGC00094190-01

NCGC00094190-02

NCGC00094190-03

NCGC00094190-04

NCGC00254654-01

NCGC00261551-01

I012

KSC-18-157-2

SMR000058390

Niclosamide 100 microg/mL in Acetonitrile

SBI-0050841.P003

AB0013423

DB-051812

VU0243604

AB00052340

EU-0100866

FT-0603220

ST50408862

EN300-92958

D00436

N 3510

AB00052340_08

AB00052340_09

A828227

Q418523

Q-201469

SR-01000076024-1

SR-01000076024-3

SR-01000076024-6

BRD-K35960502-001-06-9

BRD-K35960502-001-11-9

Z57902203

5-Chloro-N-(2-chloro-4-nitrophenyl) -2-hydroxybenzamide

5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxy-benzamide

(5-chloro-2-hydroxyphenyl)-N-(2-chloro-4-nitrophenyl)carboxamide

5-chloranyl-N-(2-chloranyl-4-nitro-phenyl)-2-oxidanyl-benzamide

Niclosamide (anhydrous), European Pharmacopoeia (EP) Reference Standard
  Experimental Data
 niclosamide

Species Dosage Unit CG Lifespan(AVG/MED days) TG Lifespan(AVG/MED days) Lifespan Change(AVG/MED%) CG Lifespan(MAX days) TG Lifespan(MAX days) Lifespan Change(MAX%) Significant Strain Gender PubMed Active Label
Caenorhabditis elegans 33 umol/L -21 NS N2 24134630 Inactive
Drosophila melanogaster 20 umol/L 45.44 42.06 -7.448 NS FEMALES 33008901 Inactive
Caenorhabditis elegans 100 umol/L 17.4 17.42 0.1034 NS N2 33008901 Inactive
Caenorhabditis elegans 10 umol/L 15.13 14.96 -1.123 NS N2 33008901 Inactive
Drosophila melanogaster 200 umol/L 44.8 48.36 7.945 NS MALES 33008901 Inactive
  Experimental Data Visualization
 niclosamide

  Statistics Data
 niclosamide

Species Lifespan Change(AVG/MED%) Lifespan Change(MAX%) Count Reference Count Data point
Caenorhabditis elegans 0.1034 2 3
Drosophila melanogaster 7.945 1 2
  Statistics Data Visualization
 niclosamide

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