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Details

Stereochemistry ABSOLUTE
Molecular Formula C22H20O13
Molecular Weight 492.3864
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARMINIC ACID

SMILES

[H][C@]1(O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C2=C(O)C(O)=C3C(=O)C4=C(C(=O)C3=C2O)C(C)=C(C(O)=O)C(O)=C4

InChI

InChIKey=DGQLVPJVXFOQEV-JNVSTXMASA-N
InChI=1S/C22H20O13/c1-4-8-5(2-6(24)9(4)22(33)34)13(25)10-11(15(8)27)16(28)12(18(30)17(10)29)21-20(32)19(31)14(26)7(3-23)35-21/h2,7,14,19-21,23-24,26,28-32H,3H2,1H3,(H,33,34)/t7-,14-,19+,20-,21+/m1/s1

HIDE SMILES / InChI

Molecular Formula C22H20O13
Molecular Weight 492.3864
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/28250351 | http://onlinelibrary.wiley.com/doi/10.2903/j.efsa.2015.4288/pdf | https://www.ncbi.nlm.nih.gov/pubmed/1385283

Carminic acid is a natural compound extracted from cochineal insects, such as the cochineal, Armenian cochineal, and Polish cochineal. . The chromophore in this molecule is the conjugated pi system extending across the central anthraquinone ring system. Carminic acid can combine with various metals to form the pigment carmine.2 In industry, it is commonly complexed with aluminum to produce a purple/pink precipitate (with calcium as a counterion). Carmine’s color differs depending on the metal it is complexed to. For centuries, carminic acid and carmine have been used as dyes. The source material is cochineal, a blood-like fluid found within the cochineal insect. Currently, carminic acid and carmine have a multitude of applications in the modern world. They are used as nontoxic food additives and biological stains and are finding new uses as electrochemical modifiers and photosensitizers.

Originator

Sources: Berichte der Deutschen Chemischen Gesellschaft Volume 23, Pages 1905-8, Journal 1906

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Severe hypertensive reaction to indigo carmine.
1977 Feb
Promoting effects of carminic acid-enriched cochineal extracts on capsular invasive thyroid carcinomas through targeting activation of angiogenesis in rats.
2012
Patents

Patents

Sample Use Guides

Acceptable daily intake 5 mg carmine (containing approximately 50 % carminic acid)/kg bw
Route of Administration: Oral
In Vitro Use Guide
In the Salmonella typhimurium reverse mutation test, carminic acid (53.1 % pure) was not mutagenic in strains TA 1535, TA 1537, TA 98 or TA 100 at doses from 125 to 2 000 μg/plate, in the presence and in the absence of S9 at two concentration levels
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:17:28 UTC 2023
Edited
by admin
on Fri Dec 15 15:17:28 UTC 2023
Record UNII
CID8Z8N95N
Record Status Validated (UNII)
Record Version
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Name Type Language
CARMINIC ACID
HSDB   MI  
Common Name English
CARMINE 5297
Common Name English
Carmine component carminic acid
Common Name English
COCHINEAL CARMINE
Common Name English
E 120
Code English
NSC-6196
Code English
2-ANTHRACENECARBOXYLIC ACID, 7-.BETA.-D-GLUCOPYRANOSYL-9,10-DIHYDRO-3,5,6,8-TETRAHYDROXY-1-METHYL-9,10-DIOXO-
Common Name English
SUN RED NO. 1
Common Name English
COCHINEAL RED PWD
Common Name English
CI 75470 [INCI]
Common Name English
NATURAL RED 2180
Common Name English
CI-NATURAL RED 4
Common Name English
C.I. 75470
Common Name English
C.I. NATURAL RED 4
Common Name English
E-120
Code English
INS-120
Code English
NSC-326224
Code English
SAN-EI GEN SAN RED 1
Common Name English
CI 75470
INCI  
INCI  
Official Name English
CARMINIC ACID [MI]
Common Name English
NATURAL RED 4
Common Name English
CI-(1975)-NO.75470
Code English
CARMINIC ACID [HSDB]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C461
Created by admin on Fri Dec 15 15:17:28 UTC 2023 , Edited by admin on Fri Dec 15 15:17:28 UTC 2023
Code System Code Type Description
FDA UNII
CID8Z8N95N
Created by admin on Fri Dec 15 15:17:28 UTC 2023 , Edited by admin on Fri Dec 15 15:17:28 UTC 2023
PRIMARY
NCI_THESAURUS
C83598
Created by admin on Fri Dec 15 15:17:28 UTC 2023 , Edited by admin on Fri Dec 15 15:17:28 UTC 2023
PRIMARY
NSC
326224
Created by admin on Fri Dec 15 15:17:28 UTC 2023 , Edited by admin on Fri Dec 15 15:17:28 UTC 2023
PRIMARY
SMS_ID
100000135667
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PRIMARY
DAILYMED
CID8Z8N95N
Created by admin on Fri Dec 15 15:17:28 UTC 2023 , Edited by admin on Fri Dec 15 15:17:28 UTC 2023
PRIMARY
NSC
6196
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PRIMARY
EVMPD
SUB71437
Created by admin on Fri Dec 15 15:17:28 UTC 2023 , Edited by admin on Fri Dec 15 15:17:28 UTC 2023
PRIMARY
ECHA (EC/EINECS)
215-023-3
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PRIMARY
PUBCHEM
10255083
Created by admin on Fri Dec 15 15:17:28 UTC 2023 , Edited by admin on Fri Dec 15 15:17:28 UTC 2023
PRIMARY
CODEX ALIMENTARIUS (GSFA)
INS-120
Created by admin on Fri Dec 15 15:17:28 UTC 2023 , Edited by admin on Fri Dec 15 15:17:28 UTC 2023
PRIMARY
MESH
C000386
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PRIMARY
RXCUI
1368643
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PRIMARY RxNorm
MERCK INDEX
m3113
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PRIMARY Merck Index
JECFA EVALUATION
INS-120
Created by admin on Fri Dec 15 15:17:28 UTC 2023 , Edited by admin on Fri Dec 15 15:17:28 UTC 2023
PRIMARY
EPA CompTox
DTXSID9022817
Created by admin on Fri Dec 15 15:17:28 UTC 2023 , Edited by admin on Fri Dec 15 15:17:28 UTC 2023
PRIMARY
WIKIPEDIA
CARMINIC ACID
Created by admin on Fri Dec 15 15:17:28 UTC 2023 , Edited by admin on Fri Dec 15 15:17:28 UTC 2023
PRIMARY
CAS
1260-17-9
Created by admin on Fri Dec 15 15:17:28 UTC 2023 , Edited by admin on Fri Dec 15 15:17:28 UTC 2023
PRIMARY
CHEBI
78310
Created by admin on Fri Dec 15 15:17:28 UTC 2023 , Edited by admin on Fri Dec 15 15:17:28 UTC 2023
PRIMARY
HSDB
912
Created by admin on Fri Dec 15 15:17:28 UTC 2023 , Edited by admin on Fri Dec 15 15:17:28 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
MAJOR
AMOUNT PRESENT