Light green SF yellowish
Identification
- Generic Name
- Light green SF yellowish
- DrugBank Accession Number
- DB11183
- Background
Light green SF yellowish is a green triarylmethane dye that is used in the preparation of the staining solution which is widely used as a counterstain. It is used in histological applications and other labratory settings, and usually exists as a disodium salt. The maximum absorption of light green SF yellowish is at 630 (422) nm. Although it has been used as a food colorant, it was discontinued from the market due to low popularity which are possibly due to low durability of the dye and increased tendency of the dye to fade. Light green SF yellowish is also available as sterile strips used as a diagnostic agent when superficial corneal or conjunctival tissue change is suspected.
- Type
- Small Molecule
- Groups
- Approved, Experimental
- Structure
- Weight
- Average: 792.848
Monoisotopic: 792.122182116 - Chemical Formula
- C37H34N2Na2O9S3
- Synonyms
- A F Green No.2
- A.F. Green No. 2
- Acid Brilliant Green SF
- Acid green
- Acid green 5
- Acid Green A
- C.I. Acid Green 5
- Lichtgruen
- Light Green G
- Light Green SF
- Wool Brilliant Green SF
Pharmacology
- Indication
Not Available
Reduce drug development failure ratesBuild, train, & validate machine-learning modelswith evidence-based and structured datasets.Build, train, & validate predictive machine-learning models with structured datasets.- Contraindications & Blackbox Warnings
- Prevent Adverse Drug Events TodayTap into our Clinical API for life-saving information on contraindications & blackbox warnings, population restrictions, harmful risks, & more.Avoid life-threatening adverse drug events with our Clinical API
- Pharmacodynamics
Not Available
- Mechanism of action
- Not Available
- Absorption
Not Available
- Volume of distribution
Not Available
- Protein binding
Not Available
- Metabolism
- Not Available
- Route of elimination
Not Available
- Half-life
Not Available
- Clearance
Not Available
- Adverse Effects
- Improve decision support & research outcomesWith structured adverse effects data, including: blackbox warnings, adverse reactions, warning & precautions, & incidence rates. View sample adverse effects data in our new Data Library!Improve decision support & research outcomes with our structured adverse effects data.
- Toxicity
Not Available
- Pathways
- Not Available
- Pharmacogenomic Effects/ADRs
- Not Available
Interactions
- Drug Interactions
- This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.Not Available
- Food Interactions
- No interactions found.
Products
- Drug product information from 10+ global regionsOur datasets provide approved product information including:dosage, form, labeller, route of administration, and marketing period.Access drug product information from over 10 global regions.
- Brand Name Prescription Products
Name Dosage Strength Route Labeller Marketing Start Marketing End Region Image GreenGlo Strip 1.5 mg/1.5mg Ophthalmic HUB Pharmaceuticals, Inc. 2012-04-01 Not applicable US - Unapproved/Other Products
Name Ingredients Dosage Route Labeller Marketing Start Marketing End Region Image GreenGlo Light green SF yellowish (1.5 mg/1.5mg) Strip Ophthalmic HUB Pharmaceuticals, Inc. 2012-04-01 Not applicable US
Categories
- Drug Categories
- Chemical TaxonomyProvided by Classyfire
- Description
- This compound belongs to the class of organic compounds known as phenylbenzamines. These are aromatic compounds consisting of a benzyl group that is N-linked to a benzamine.
- Kingdom
- Organic compounds
- Super Class
- Benzenoids
- Class
- Benzene and substituted derivatives
- Sub Class
- Phenylmethylamines
- Direct Parent
- Phenylbenzamines
- Alternative Parents
- Diphenylmethanes / Benzenesulfonic acids and derivatives / Benzenesulfonyl compounds / 1-sulfo,2-unsubstituted aromatic compounds / Dialkylarylamines / Benzylamines / Aniline and substituted anilines / Aralkylamines / Organosulfonic acids / Sulfonyls show 7 more
- Substituents
- 1-sulfo,2-unsubstituted aromatic compound / Amine / Aniline or substituted anilines / Aralkylamine / Aromatic homomonocyclic compound / Arylsulfonic acid or derivatives / Azomethine / Benzenesulfonate / Benzenesulfonyl group / Benzylamine show 22 more
- Molecular Framework
- Aromatic homomonocyclic compounds
- External Descriptors
- organic sodium salt (CHEBI:87065)
- Affected organisms
- Not Available
Chemical Identifiers
- UNII
- 3F7BHA64Z0
- CAS number
- 5141-20-8
- InChI Key
- DGOBMKYRQHEFGQ-UHFFFAOYSA-L
- InChI
- InChI=1S/C37H36N2O9S3.2Na/c1-3-38(25-27-7-5-9-35(23-27)50(43,44)45)32-17-11-29(12-18-32)37(31-15-21-34(22-16-31)49(40,41)42)30-13-19-33(20-14-30)39(4-2)26-28-8-6-10-36(24-28)51(46,47)48;;/h5-24H,3-4,25-26H2,1-2H3,(H2-,40,41,42,43,44,45,46,47,48);;/q;2*+1/p-2
- IUPAC Name
- disodium 4-[(4-{ethyl[(3-sulfophenyl)methyl]amino}phenyl)[(1Z,4Z)-4-{ethyl[(3-sulfophenyl)methyl]iminiumyl}cyclohexa-2,5-dien-1-ylidene]methyl]benzene-1-sulfonate
- SMILES
- [Na+].[Na+].CCN(CC1=CC(=CC=C1)S([O-])(=O)=O)C1=CC=C(C=C1)C(C1=CC=C(C=C1)S([O-])(=O)=O)=C1C=CC(C=C1)=[N+](CC)CC1=CC(=CC=C1)S([O-])(=O)=O
References
- General References
- Not Available
- External Links
Clinical Trials
Pharmacoeconomics
- Manufacturers
- Not Available
- Packagers
- Not Available
- Dosage Forms
Form Route Strength Strip Ophthalmic 1.5 mg/1.5mg - Prices
- Not Available
- Patents
- Not Available
Properties
- State
- Not Available
- Experimental Properties
- Not Available
- Predicted Properties
Property Value Source Water Solubility 7.65e-05 mg/mL ALOGPS logP 2.08 ALOGPS logP 2.68 Chemaxon logS -7 ALOGPS pKa (Strongest Acidic) -2.3 Chemaxon pKa (Strongest Basic) 3.52 Chemaxon Physiological Charge -2 Chemaxon Hydrogen Acceptor Count 10 Chemaxon Hydrogen Donor Count 0 Chemaxon Polar Surface Area 177.85 Å2 Chemaxon Rotatable Bond Count 12 Chemaxon Refractivity 218.8 m3·mol-1 Chemaxon Polarizability 77.18 Å3 Chemaxon Number of Rings 5 Chemaxon Bioavailability 0 Chemaxon Rule of Five No Chemaxon Ghose Filter No Chemaxon Veber's Rule No Chemaxon MDDR-like Rule Yes Chemaxon - Predicted ADMET Features
- Not Available
Spectra
- Mass Spec (NIST)
- Not Available
- Spectra
Spectrum Spectrum Type Splash Key Predicted GC-MS Spectrum - GC-MS Predicted GC-MS splash10-000l-1000019300-04b04153c907756291f3 - Chromatographic Properties
Collision Cross Sections (CCS)
Adduct CCS Value (Å2) Source type Source [M-H]- 313.5578319 predictedDarkChem Lite v0.1.0 [M-H]- 243.15558 predictedDeepCCS 1.0 (2019) [M+H]+ 312.4276319 predictedDarkChem Lite v0.1.0 [M+H]+ 245.21788 predictedDeepCCS 1.0 (2019) [M+Na]+ 251.13042 predictedDeepCCS 1.0 (2019)
Drug created at December 03, 2015 16:51 / Updated at June 12, 2020 16:53