Compound Summary


Rutaecarpine
  Compound Information
 Rutaecarpine

Compound Name:

Rutaecarpine

Compound CID:

65752

Synonyms:

Rutaecarpine

84-26-4

Rutecarpine

Rutacarpine

Rhetine

More...

Iupac Name:

3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4,6,8,15,17,19-octaen-14-one

InChI:

InChI=1S/C18H13N3O/c22-18-13-6-2-4-8-15(13)20-17-16-12(9-10-21(17)18)11-5-1-3-7-14(11)19-16/h1-8,19H,9-10H2

InChIKey:

ACVGWSKVRYFWRP-UHFFFAOYSA-N

Canonical Smiles:

C1CN2C(=NC3=CC=CC=C3C2=O)C4=C1C5=CC=CC=C5N4

Isomeric Smiles:

C1CN2C(=NC3=CC=CC=C3C2=O)C4=C1C5=CC=CC=C5N4

Molecular Weight:

287.3

Molecular Formula:

C18H13N3O

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

Molecular Weight:

287.3

Molecular Formula:

C18H13N3O

Hydrogen Bond Donor Count:

1

Hydrogen Bond Acceptor Count:

2

Rotatable Bond Count:

0

Heavy Atom Count:

22

Complexity:

517

  Synonyms
 Rutaecarpine

Rutaecarpine Rutaecarpine

Rutaecarpine

84-26-4

Rutecarpine

Rutacarpine

Rhetine

Rutaecarpin

C18H13N3O

UNII-8XZV289PRY

8,13-dihydroindolo2,3:3,4pyrido2,1-bquinazolin-5(7H)-one"

Indolo2,3:3,4pyrido2,1-bquinazolin-5(7H)-one, 8,13-dihydro-

MFCD00210551

8XZV289PRY

CHEMBL85139

CHEBI:8922

7,8-dihydroindolo2,3:3,4pyrido2,1-bquinazolin-5(13H)-one"

8,13-Dihydro-indolo2,3:3,4pyrido2,1-bquinazolin-5(7H)-one"

Indolo(2,3:3,4)pyrido(2,1-b)quinazolin-5(7H)-one, 8,13-dihydro-

3,13,21-triazapentacyclo11.8.0.0^{2,10}.0^{4,9}.0^{15,20}henicosa-1(21),2(10),4,6,8,15,17,19-octaen-14-one

SMR001230721

SR-01000076104

NSC 258317

8,13-dihydro-Indolo(2,3:3,4)pyrido(2,1-b)quinazolin-5(7H)-one

Rutaecarpine,(S)

Rutecarpine (8CI)

Lopac-R-3277

Rutaecarpine (Rutecarpine)

UPCMLD-DP040

Lopac0_001091

Oprea1_313284

cid_65752

MLS002153304

MLS006011796

SCHEMBL288507

Rutaecarpine, >98% (HPLC)

UPCMLD-DP040:001

DTXSID00232884

HMS2233M24

HMS3263K04

HMS3374B10

HMS3656C09

HMS3884P13

ZINC898237

ALBB-028246

BCP21309

HY-N0147

Tox21_501091

BBL028393

BDBM50131046

NSC258317

s2349

STL146385

AKOS005720935

CCG-205168

CS-6160

GS-3618

LP01091

MCULE-8799347749

NSC-258317

SDCCGSBI-0051061.P002

SMP2_000103

NCGC00015892-01

NCGC00015892-02

NCGC00015892-03

NCGC00015892-04

NCGC00015892-05

NCGC00015892-06

NCGC00015892-07

NCGC00015892-08

NCGC00015892-13

NCGC00094364-01

NCGC00094364-03

NCGC00094364-04

NCGC00261776-01

AC-34838

NCI60_002069

1,1-Hexamethylenebis (3,3-dimethylurea)

AB0019845

EU-0101091

FT-0653229

N1344

R0102

SW220226-1

V0371

C09238

H10091

J10443

R 3277

210R551

A864154

Q-100850

SR-01000076104-2

SR-01000076104-6

Q15424771

Indolo2,4pyrido2,1-bquinazolin-5(7H)-one, 8,13-dihydro-"

8,13-Dihydro-7H-indolo2,3:3,4pyrido2,1-bquinazolin-5-one

6,7-Imino(1,2-phenylene)-8,9-dihydro-11H-pyrido2,1-bquinazoline-11-one

Indolo(2,3:3,4)pyrido(2,1-b)quinazolin-5(7H)-one, 8,13-dihydro- (9CI)

3,13,21-triazapentacyclo11.8.0.0^{2,10}.0^{4,9}.0^{15,20}henicosa-1(21),2(10),4(9),5,7,15(20),16,18-octaen-14-one

3,13,21-triazapentacyclo11.8.0.02,10.04,9.015,20henicosa-1(21),2(10),4,6,8,15,17,19-octaen-14-one

  Experimental Data
 Rutaecarpine

Species Dose Unit Control(Avg days) Treatment(Avg days) Avg/Med Lifespan Change(%) Control(Max days) Treatment(Max days) Max Lifespan Change(%) Significant Strain Gender PubMed Avg/Med Lifespan Change tab
Caenorhabditis elegans 33.000000000000000 umol/L -3.000000000000000 NS N2 24134630 Inactive
  Experimental Data Visualization
 Rutaecarpine

  Statistics Data
 Rutaecarpine

Species Avg/Med Lifespan Change(%) Max Lifespan Change(%) Count Reference Count Data point
Caenorhabditis elegans -3.000000000000000 1 1
  Statistics Data Visualization
 Rutaecarpine