Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Herb: 2Ingredient: 1Target: 12Links: 14
Arranging relationship network...
Record Fields
Scalar fields from the final ingredient record.
- Ingredient Id
- 20446
- Core Entity Id
- 25908
- Source Entity Count
- 1
- Preferred Name
- Glv
- Name En
- Glyoxylic acid
- Pubchem Id
- 760
- Smiles Canonical
- C(=O)C(=O)O
- Molecular Formula
- C2H2O3
- Molecular Weight
- 74.0350
- Inchikey
- HHLFWLYXYJOTON-UHFFFAOYSA-N
- Inchi
- InChI=1S/C2H2O3/c3-1-2(4)5/h1H,(H,4,5)
- Isomeric Smiles
- C(=O)C(=O)O
- Cas Id
- 298-12-4
- Ob Score
- 32.2456
- Mol Logp
- -0.7301
- Num H Donors
- 1
- Num H Acceptors
- 2
- Num Rotatable Bonds
- 1
- Drug Likeness
- 0.3290
- Polar Surface Area
- Molecular Volume
- Alogp
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Glv
Role
Molecule_name
Source
SymMap_v2
Preferred
Yes
Name
GLV
Role
preferred
Source
TCMBank
Preferred
Yes
Name
GLV
Role
preferred
Source
ETCM_v2
Preferred
Yes
Name
Glv
Role
preferred
Source
SymMap_v2
Preferred
Yes
Name
Glv
Role
preferred
Source
HERB_v2
Preferred
Yes
Name
Glv
Role
preferred
Source
itcmdb_public
Preferred
Yes
Name
.alpha.-Ketoacetic acid
Role
alias
Source
TCMBank
Preferred
No
Name
2-Oxo acid
Role
alias
Source
TCMBank
Preferred
No
Name
2-Oxoacetic Acid
Role
alias
Source
itcmdb_public
Preferred
No
Name
2-Oxoacetic Acid
Role
alias
Source
HERB_v2
Preferred
No
Name
2-oxo carboxylic acids
Role
alias
Source
TCMBank
Preferred
No
Name
2-oxo monocarboxylic acids
Role
alias
Source
TCMBank
Preferred
No
Name
260150_ALDRICH
Role
alias
Source
TCMBank
Preferred
No
Name
298-12-4
Role
alias
Source
HERB_v2
Preferred
No
Name
298-12-4
Role
alias
Source
TCMBank
Preferred
No
Name
298-12-4
Role
alias
Source
itcmdb_public
Preferred
No
Name
4-03-00-01489 (Beilstein Handbook Reference)
Role
alias
Source
TCMBank
Preferred
No
Name
50711_FLUKA
Role
alias
Source
TCMBank
Preferred
No
Name
Acetic acid, oxo-
Role
alias
Source
TCMBank
Preferred
No
Name
Acetic acid, oxo-
Role
alias
Source
itcmdb_public
Preferred
No
Name
Acetic acid, oxo-
Role
alias
Source
HERB_v2
Preferred
No
Name
Acetic acid, oxo- (9CI)
Role
alias
Source
TCMBank
Preferred
No
Name
BRN 0741891
Role
alias
Source
TCMBank
Preferred
No
Name
C00048
Role
alias
Source
TCMBank
Preferred
No
Name
CCRIS 1455
Role
alias
Source
TCMBank
Preferred
No
Name
CHEBI:16891
Role
alias
Source
TCMBank
Preferred
No
Name
CHEBI:35910
Role
alias
Source
TCMBank
Preferred
No
Name
EINECS 206-058-5
Role
alias
Source
TCMBank
Preferred
No
Name
Formic acid, formyl-
Role
alias
Source
TCMBank
Preferred
No
Name
Formylformic acid
Role
alias
Source
TCMBank
Preferred
No
Name
Formylformic acid
Role
alias
Source
HERB_v2
Preferred
No
Name
Formylformic acid
Role
alias
Source
itcmdb_public
Preferred
No
Name
G1134_SIGMA
Role
alias
Source
TCMBank
Preferred
No
Name
GLYOX
Role
alias
Source
TCMBank
Preferred
No
Name
GLYOXALATE, GLYOXYLATE
Role
alias
Source
TCMBank
Preferred
No
Name
Glyoxalic acid
Role
alias
Source
HERB_v2
Preferred
No
Name
Glyoxalic acid
Role
alias
Source
TCMBank
Preferred
No
Name
Glyoxalic acid
Role
alias
Source
itcmdb_public
Preferred
No
Name
Glyoxalsaeure
Role
alias
Source
TCMBank
Preferred
No
Name
Glyoxylic acid (8CI)
Role
alias
Source
TCMBank
Preferred
No
Name
Glyoxylic acid solution
Role
alias
Source
TCMBank
Preferred
No
Name
Glyoxylsaeure
Role
alias
Source
TCMBank
Preferred
No
Name
HSDB 5559
Role
alias
Source
TCMBank
Preferred
No
Name
Kyselina glyoxylova [Czech]
Role
alias
Source
TCMBank
Preferred
No
Name
NSC 27785
Role
alias
Source
TCMBank
Preferred
No
Name
Oxalaldehydic acid
Role
alias
Source
itcmdb_public
Preferred
No
Name
Oxalaldehydic acid
Role
alias
Source
HERB_v2
Preferred
No
Name
Oxalaldehydic acid
Role
alias
Source
TCMBank
Preferred
No
Name
Oxoacetic acid
Role
alias
Source
HERB_v2
Preferred
No
Name
Oxoacetic acid
Role
alias
Source
TCMBank
Preferred
No
Name
Oxoacetic acid
Role
alias
Source
itcmdb_public
Preferred
No
Name
Oxoethanoic acid
Role
alias
Source
HERB_v2
Preferred
No
Name
Oxoethanoic acid
Role
alias
Source
TCMBank
Preferred
No
Name
Oxoethanoic acid
Role
alias
Source
itcmdb_public
Preferred
No
Name
WLN: VHVQ
Role
alias
Source
TCMBank
Preferred
No
Name
glyoxalate
Role
alias
Source
TCMBank
Preferred
No
Name
glyoxylic acid
Role
alias
Source
HERB_v2
Preferred
No
Name
glyoxylic acid
Role
alias
Source
TCMBank
Preferred
No
Name
glyoxylic acid
Role
alias
Source
itcmdb_public
Preferred
No
Name
oxaldehydic acid
Role
alias
Source
HERB_v2
Preferred
No
Name
oxaldehydic acid
Role
alias
Source
TCMBank
Preferred
No
Name
oxaldehydic acid
Role
alias
Source
itcmdb_public
Preferred
No
Aliases
Additional names normalized into the restored final schema.
.alpha.-Ketoacetic acid2-Oxo acid2-Oxoacetic Acid2-oxo carboxylic acids2-oxo monocarboxylic acids260150_ALDRICH298-12-44-03-00-01489 (Beilstein Handbook Reference)50711_FLUKAAcetic acid, oxo-Acetic acid, oxo- (9CI)BRN 0741891C00048CCRIS 1455CHEBI:16891CHEBI:35910EINECS 206-058-5Formic acid, formyl-Formylformic acidG1134_SIGMAGLYOXGLYOXALATE, GLYOXYLATEGlyoxalic acidGlyoxalsaeureGlyoxylic acid (8CI)Glyoxylic acid solutionGlyoxylsaeureHSDB 5559Kyselina glyoxylova [Czech]NSC 27785Oxalaldehydic acidOxoacetic acidOxoethanoic acidWLN: VHVQglyoxalateglyoxylic acidoxaldehydic acid
Cross References
Trusted external identifiers retained for this final record.
Cas
298-12-4
Herb
HBIN028075
Npass
NPC307812
Tcmsp
MOL002686
Sym Map
SMIT04884
Pub Chem
760
Tcmbank
TCMBANKIN019814
Etcm Ingredient
GLV
Itcmdb Generated
ITX-INGREDIENT-9BB4F0A42241
Attributes
Merged source attributes and domain-specific metadata.
Type
Other ingredients
In Ch I
InChI=1S/C2H2O3/c3-1-2(4)5/h1H,(H,4,5)
Mol Wt
74.035
Cas Id
298-12-4
Smiles
C(=O)C(=O)O
Mol Log P
-0.7301
Version
v1,v2
In Ch Ikey
HHLFWLYXYJOTON-UHFFFAOYSA-N
Ob Score
32.2455656732.24556632.246
Suppress
0
Num Hdonors
1
Drug Likeness
0.329
Num Hacceptors
2
Isomeric Smiles
C(=O)C(=O)O
Molecule Weight
74.04
Canonical Smiles
C(=O)C(=O)O
Herb Alias Names
glyoxylic acid298-12-42-Oxoacetic AcidGlyoxalic acidOxoacetic acidOxoethanoic acidFormylformic acidAcetic acid, oxo-Oxalaldehydic acidoxaldehydic acid
Molecular Weight
74.000
Molecular Weight
74.04
Molecular Formula
C2H2O3
Molecular Formula
C2H2O3
Molecular Formula
C2H2O3
Num Rotatable Bonds
1
Fda Maximum Daily Dose (Fdamdd)
0.010
Quantitative Estimate Of Drug Likeness（Qed）
0.329