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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:90695 - anthra[1,9-
cd
]pyrazol-6(2
H
)-one
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ChEBI Name
anthra[1,9-
cd
]pyrazol-6(2
H
)-one
ChEBI ID
CHEBI:90695
ChEBI ASCII Name
anthra[1,9-cd]pyrazol-6(2H)-one
Definition
A member of the class of anthrapyrazoles that is anthra[1,9-
cd
]pyrazole substituted at position 6 by an oxo group. An inhibitor of c-Jun
N
-terminal kinase.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C14H8N2O
Net Charge
0
Average Mass
220.231
Monoisotopic Mass
220.06366
InChI
InChI=1S/C14H8N2O/c17-14-9-5-2-1-4-8(9)13-12-10(14)6-3-7-11(12)15-16-13/h1-7H,(H,15,16)
InChIKey
ACPOUJIDANTYHO-UHFFFAOYSA-N
SMILES
O=C1C2=CC=CC3=C2C(=NN3)C2=C1C=CC=C2
Roles Classification
Biological Role
(s):
c-Jun N-terminal kinase inhibitor
An EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor that inhibits the action of
c-Jun N-terminal kinase
.
Application
(s):
geroprotector
Any compound that supports healthy aging, slows the biological aging process, or extends lifespan.
antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
anthra[1,9-
cd
]pyrazol-6(2
H
)-one (
CHEBI:90695
)
has role
antineoplastic agent (
CHEBI:35610
)
anthra[1,9-
cd
]pyrazol-6(2
H
)-one (
CHEBI:90695
)
has role
c-Jun N-terminal kinase inhibitor (
CHEBI:90172
)
anthra[1,9-
cd
]pyrazol-6(2
H
)-one (
CHEBI:90695
)
has role
geroprotector (
CHEBI:176497
)
anthra[1,9-
cd
]pyrazol-6(2
H
)-one (
CHEBI:90695
)
is a
anthrapyrazole (
CHEBI:90698
)
anthra[1,9-
cd
]pyrazol-6(2
H
)-one (
CHEBI:90695
)
is a
aromatic ketone (
CHEBI:76224
)
anthra[1,9-
cd
]pyrazol-6(2
H
)-one (
CHEBI:90695
)
is a
cyclic ketone (
CHEBI:3992
)
IUPAC Name
dibenzo[
cd,g
]indazol-6(2
H
)-one
Synonyms
Sources
1,9-Pyrazoloanthrone
ChemIDplus
2
H
-dibenzo[
cd,g
]indazol-6-one
ChEBI
C.I. 70300
ChemIDplus
Pyrazolanthrone
ChemIDplus
Pyrazoleanthrone
ChemIDplus
SP 600125
ChEBI
SP600125
ChEBI
Manual Xrefs
Databases
1,9-Pyrazoloanthrone
Wikipedia
537
PDBeChem
DB01782
DrugBank
LSM-1163
LINCS
View more database links
Registry Numbers
Types
Sources
129-56-6
CAS Registry Number
ChemIDplus
746890
Reaxys Registry Number
Reaxys
Citations
Types
Sources
22363408
PubMed citation
Europe PMC
25866226
PubMed citation
Europe PMC
26465378
PubMed citation
Europe PMC
26704630
PubMed citation
Europe PMC
27005940
PubMed citation
Europe PMC
27924151
PubMed citation
Europe PMC
29273684
PubMed citation
Europe PMC
29409910
PubMed citation
Europe PMC
31105818
PubMed citation
Europe PMC
31685029
PubMed citation
Europe PMC
33520960
PubMed citation
Europe PMC
33546770
PubMed citation
Europe PMC
34014386
PubMed citation
Europe PMC
34437475
PubMed citation
Europe PMC
34486378
PubMed citation
Europe PMC
Last Modified
28 October 2021