Basic information
- CAS
59865-13-3- Standard SMILES
C/C=C/CC(C)C(O)C1C(=O)NC(CC)C(=O)N(C)CC(=O)N(C)C(CC(C)C)C(=O)NC(C(C)C)C(=O)N(C)C(CC(C)C)C(=O)NC(C)C(=O)NC(C)C(=O)N(C)C(CC(C)C)C(=O)N(C)C(CC(C)C)C(=O)N(C)C(C(C)C)C(=O)N1C- InChIKey
PMATZTZNYRCHOR-IMVLJIQESA-N- Molecular formula
- C62H111N11O12
- Average molar mass
- 1,202.6 g/mol
- Monoisotopic mass
- 1,201.84136802
Names & identifiers
- Preferred name
- Cyclosporine (USP)
- IUPAC
- 30-ethyl-33-[(E)-1-hydroxy-2-methylhex-4-enyl]-1,4,7,10,12,15,19,25,28-nonamethyl-6,9,18,24-tetrakis(2-methylpropyl)-3,21-di(propan-2-yl)-1,4,7,10,13,16,19,22,25,28,31-undecazacyclotritriacontane-2,5,8,11,14,17,20,23,26,29,32-undecone
- English name
- Cyclosporin A
- Molecular formula
- C62H111N11O12
- Molecular weight
- 1202.61
Names & synonyms
Show more names
Database identifiers
- CAS
59865-13-3- PubChem CID
- 5280754
Properties
Computed structural properties
- XLogP
- 7.5
- Topological polar surface area
- 279 Ų
- Hydrogen bond donors
- 5
- Hydrogen bond acceptors
- 12
- Rotatable bonds
- 15
- Heavy atoms
- 85
- Formal charge
- 0
- Complexity
- 2,330
Physicochemical properties
- Melting point
- 148 · 148-151°C
- Boiling point
- 838.63 °C · 838.63°C (rough estimate)
- alpha
- 20 · D20 -244° (c = 0.6 in chloroform); D20 -189° (c = 0.5 in methanol)
- Density
- 0.9913 · 0.9913 (rough estimate)
- refractive index
- 1.65 · 1.6500 (estimate)
- Flash point
- 87 ℃ · 87℃
- storage temp.
- -20 °C · -20°C
- solubility
- 30 mg/mL · ethanol: 30 mg/mL
- form
- solid
- pka
- 13.32 · 13.32±0.70(Predicted)
- color
- white
- optical activity
- -18922 · -18922 (methanol)
- Water Solubility
- Soluble in dimethyl sulfoxide and ethanol. Insoluble in water.
- Merck
- 14 · 14,2752
- BRN
- 3647785 · 3647785
- Stability
- 3 years · Stable for 3 years as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
- InChIKey
- PMATZTZNYRCHOR-CGLBZJNRSA-N
- CAS DataBase Reference
- 59865 · 59865-13-3(CAS DataBase Reference)
- EWG's Food Scores
- 4 · 4
- NCI Dictionary of Cancer Terms
- cyclosporine
- FDA UNII
- 83 HN0GTJ6D · 83HN0GTJ6D
- NCI Drug Dictionary
- cyclosporine
- ATC code
- 4 AD01,S01XA18 · L04AD01,S01XA18
- Proposition 65 List
- Ciclosporin (Cyclosporin A; Cyclosporine)
- IARC
- 1 · 1 (Vol. 50, 100A) 2012
- EPA Substance Registry System
- Cyclosporin A (59865-13-3)
- UNSPSC Code
- 41116107 · 41116107
- NACRES
- 77 · NA.77
- Protein binding
- 90 % · Approx 90%
- Excreted unchanged in urine
- 0.1 % · 0.1%
- Volume of distribution
- 3 · 3-5(L/kg)
- Biological half-life
- 5 · 5-20 / Unchanged
- Symbol(GHS)
- 7 · GHS07,GHS08
- Signal word
- Danger
- Hazard statements
- 302 · H302-H350-H360FD
- Precautionary statements
- 201 · P201-P202-P264-P270-P301+P312-P308+P313
- Hazard Codes
- T,Xn,F
- Risk Statements
- 45 · 45-60-22-40-36-20/21/22-11
- Safety Statements
- 53 · 53-45-36/37-24/25-22-26-16
- RIDADR
- 1648 · UN 1648 3 / PGII
- WGK Germany
- 3 · 3
- RTECS
- 4120000 · GZ4120000
- HS Code
- 29419090 · 29419090
- Storage Class
- 10 · 10 - Combustible liquids
- Hazardous Substances Data
- 59865 · 59865-13-3(Hazardous Substances Data)
- Toxicity
- 50 in · LD50 in mice, rats, rabbits (mg/kg): 107, 25, >10 i.v.; 2329, 1480, >1000 orally (Ryffel)
Safety & regulation
Safety data
- wgk
- 3
- rtecs
- GZ4120000
- ridadr
- UN 1648 3 / PGII
- hs_code
- 29419090
- Toxicity
- LD50 in mice, rats, rabbits (mg/kg): 107, 25, >10 i.v.; 2329, 1480, >1000 orally (Ryffel)
- risk_code
- 45-60-22-40-36-20/21/22-11
- Signal word
- Danger
- Symbol(GHS)
- GHS07,GHS08
- hazard_code
- T,Xn,F
- safety_code
- 53-45-36/37-24/25-22-26-16
- Storage Class
- 10 - Combustible liquids
- Hazard statements
- H302-H350-H360FD
- Precautionary statements
- P201-P202-P264-P270-P301+P312-P308+P313
- Hazardous Substances Data
- 59865-13-3(Hazardous Substances Data)
Chemistry & industry
Applications
DescriptionCyclosporine A is a powerful immunosuppressive drug intended for preventing rejection of kidney, heart, and lung transplants. A new era in the development of immunopharmacology began with the discovery of cyclosporines. Cyclosporines are produced by mycelial mushrooms Tolypocladium inflatum, Tricoderma polysporum, and Cylindrocarpon lucidum, which are found in the ground.Cyclosporine A is the first drug to affect a specific line of protecting cells of the body. Unlike usual cytotoxics, it suppresses T-cells and acts on all cell lines simultaneously. Cyclosporine A significantly eases the ‘reception’ of transplants, and increases the possibility of treating autoimmune system diseases.
UsesAn immunosuppressant that has revolutionized organ transplantation through its use in the prevention of graft rejection. A group of nonpolar cyclic oligopeptides with immunosupppressant activity.
Usesprothrombogenic agent
UsesCyclosporin A is a hydrophobic cyclic peptide isolated from several fungal species including Cylindrocarpon, Fusarium, Trichoderma and Tolypocladium. Cyclosporin A inhibits T-cell activation and has been marketed since 1983 as an immunosuppressant in post-allogeneic organ transplant. Cyclosporin A acts by binding to the protein, cyclophilin (immunophilin), in T-lymphocytes causing inhibition of calcineurin (protein phosphatase 2B). Cyclosporin A reduces transcription of interleukin 2, and inhibits lymphokine production, interleukin release and NO synthesis induced by interleukin 1α, lipopolysaccharides and TNFα.
General DescriptionWhite prismatic needles (from acetone) or white powder.
DescriptionCyclosporin is a cyclic polypeptide immunosuppressant agent consisting of 11 amino acids and having a molecular weight of 1202.64. It is produced as a metabolite by the fungus species Beauveria nlyea. Chemically, cyclosporin is designated as [R-[R*,R*-(E)]]-cyclic(L-alanyl-D- alanyl-N-methyl-L-leucyl-N-methyl-L-leucyl-N-methyl-L-valyl-3-hydroxy-N, 4-dimethyl-L-2-amino-6-octenoyl-L-a-amino-butyryl- N-methylglycyl-N- methyl-L-leucyl-L-valyl-N-methyl-L-leucyl). Molecular Formula: C62H111N11O12.
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers100 total
Additional notes
DefinitionChEBI: A cyclic nonribosomal peptide of eleven amino acids; an immunosuppressant drug widely used in post-allogeneic organ transplant to reduce the activity of the patient's immune system, and therefore the risk of organ rejection. Also causes reversible inhibiti n of immunocompetent lymphocytes in the G0- and G1-phase of the cell cycle.
Related reactions
Compound notes
Loading…