ademetionine ๐Ÿถ Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | PK/Tox | Related Drugs | BioActivity |

Stem definitionDrug idCAS RN
2414 29908-03-0

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • ademetionin
  • methioninyl adenylate
  • s-adenosylmethionine
  • ademetionine
  • donamet
Physiologic methyl radical donor involved in enzymatic transmethylation reactions and present in all living organisms. It possesses anti-inflammatory activity and has been used in treatment of chronic liver disease. (From Merck, 11th ed)
  • Molecular weight: 398.44
  • Formula: C15H22N6O5S
  • CLOGP: -4.28
  • LIPINSKI: 1
  • HAC: 11
  • HDO: 4
  • TPSA: 185.46
  • ALOGS: -2.45
  • ROTB: 7

Drug dosage:

None

ADMET properties:

PropertyValueReference
MRTD (Maximum Recommended Therapeutic Daily Dose) 62.74 ยตM/kg/day Contrera JF, Matthews EJ, Kruhlak NL, Benz RD
BA (Bioavailability) 2.50 % Kim MT, Sedykh A, Chakravarti SK, Saiakhov RD, Zhu H

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
kinase-safety-class ACVR2B,AXL,CAMK2D,CDK5,CDK9,DYRK1B,EIF2AK3,FLT3,GRK2,ITK,MAP3K21,PDK1,PDK2,PIK3CD,PRKDC 15
kinase-selectivity-class MAP2K6 1
pfas-class PFAS structural alert (1 = True, 0 = False) 0

Approvals:

None

FDA Adverse Event Reporting System (Female)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Confabulation 122.21 34.01 16 795 304 90627332
Serotonin syndrome 74.65 34.01 23 788 37864 90589772
Nystagmus 72.40 34.01 16 795 7211 90620425
Drug interaction 63.58 34.01 36 775 276417 90351219
Right aortic arch 57.76 34.01 8 803 234 90627402
Rhabdomyolysis 56.20 34.01 20 791 51236 90576400
Congenital arterial malformation 55.25 34.01 8 803 323 90627313
Dyskinesia 46.73 34.01 16 795 36518 90591118
Mechanical urticaria 43.20 34.01 7 804 597 90627039

FDA Adverse Event Reporting System (Male)

None

FDA Adverse Event Reporting System (Geriatric)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Confabulation 113.07 32.95 16 1058 505 110587720
Nystagmus 63.56 32.95 16 1058 11561 110576664
Serotonin syndrome 62.68 32.95 23 1051 59130 110529095
Rhabdomyolysis 46.91 32.95 23 1051 120378 110467847
Drug interaction 43.47 32.95 37 1037 500146 110088079
Dyskinesia 40.08 32.95 16 1058 51430 110536795
Mechanical urticaria 35.82 32.95 6 1068 577 110587648
Clonus 33.12 32.95 9 1065 8707 110579518

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC A16AA02 ALIMENTARY TRACT AND METABOLISM
OTHER ALIMENTARY TRACT AND METABOLISM PRODUCTS
OTHER ALIMENTARY TRACT AND METABOLISM PRODUCTS
Amino acids and derivatives
CHEBI has role CHEBI:23354 coenzymes
CHEBI has role CHEBI:23357 cofactor
CHEBI has role CHEBI:27027 trace elements
CHEBI has role CHEBI:50733 Dietary Supplement
CHEBI has role CHEBI:75772 S. cerevisiae metabolites
CHEBI has role CHEBI:77746 Homo sapiens metabolite
CHEBI has role CHEBI:131604 Mycoplasma genitalium metabolites

Related Drugs by ATC class:

A16AA Amino acids and derivatives 6 drugs

Drug Use | Suggest Off label Use Form| |View source of the data|

DiseaseRelationSNOMED_IDDOID
Hypertensive disorder contraindication 38341003 DOID:10763
Hyperlipidemia contraindication 55822004 DOID:1168
Diabetes mellitus contraindication 73211009 DOID:9351




๐Ÿถ Veterinary Drug Use

None

๐Ÿถ Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 2.53 acidic
pKa2 12.47 acidic
pKa3 9.91 Basic
pKa4 3.95 Basic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
Protein arginine N-methyltransferase 1 Enzyme IC50 4.92 CHEMBL
Phenylethanolamine N-methyltransferase Enzyme Kd 5.32 CHEMBL
Protein-beta-aspartate methyltransferase Enzyme Ki 4.32 CHEMBL
S-adenosylmethionine decarboxylase proenzyme Enzyme Ki 4.22 CHEMBL
Met repressor Transcription factor Kd 8.40 CHEMBL
NS5 Enzyme Kd 5.59 CHEMBL

External reference:

IDSource
4021429 VUID
N0000148840 NUI
D07128 KEGG_DRUG
4021429 VANDF
C0036002 UMLSCUI
SAM PDB_CHEM_ID
CHEMBL1088977 ChEMBL_ID
DB00118 DRUGBANK_ID
C011501 MESH_SUPPLEMENTAL_RECORD_UI
5479 INN_ID
7LP2MPO46S UNII
34755 PUBCHEM_CID
9504 RXNORM
27892 MMSL
365023 MMSL
d04524 MMSL
004313 NDDF
008834 NDDF
441671005 SNOMEDCT_US
441816007 SNOMEDCT_US
D012436 MESH_DESCRIPTOR_UI
CHEBI:15414 CHEBI
4786 IUPHAR_LIGAND_ID
7LP2MPO46S INXIGHT DRUGS

Pharmaceutical products:

None