API Export of Rapacuronium obtained from Indian Customs Trade Statistics

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Chemistry

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Also known as: Raplon, 156137-99-4, Org 9487, Org-9487, 156137-99-4 (bromide), 65q4qdg4kc
Molecular Formula
C37H61BrN2O4
Molecular Weight
677.8  g/mol
InChI Key
LVQTUXZKLGXYIU-GWSNJHLMSA-M
FDA UNII
65Q4QDG4KC

Rapacuronium
1 2D Structure

Rapacuronium

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
[(2S,3S,5S,8R,9S,10S,13S,14S,16S,17R)-3-acetyloxy-10,13-dimethyl-2-piperidin-1-yl-16-(1-prop-2-enylpiperidin-1-ium-1-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl] propanoate;bromide
2.1.2 InChI
InChI=1S/C37H61N2O4.BrH/c1-6-20-39(21-12-9-13-22-39)32-24-30-28-15-14-27-23-33(42-26(3)40)31(38-18-10-8-11-19-38)25-37(27,5)29(28)16-17-36(30,4)35(32)43-34(41)7-2;/h6,27-33,35H,1,7-25H2,2-5H3;1H/q+1;/p-1/t27-,28+,29-,30-,31-,32-,33-,35-,36-,37-;/m0./s1
2.1.3 InChI Key
LVQTUXZKLGXYIU-GWSNJHLMSA-M
2.1.4 Canonical SMILES
CCC(=O)OC1C(CC2C1(CCC3C2CCC4C3(CC(C(C4)OC(=O)C)N5CCCCC5)C)C)[N+]6(CCCCC6)CC=C.[Br-]
2.1.5 Isomeric SMILES
CCC(=O)O[C@H]1[C@H](C[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC[C@@H]4[C@@]3(C[C@@H]([C@H](C4)OC(=O)C)N5CCCCC5)C)C)[N+]6(CCCCC6)CC=C.[Br-]
2.2 Other Identifiers
2.2.1 UNII
65Q4QDG4KC
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Org 9487

2. Org-9487

3. Rapacuronium

4. Raplon

2.3.2 Depositor-Supplied Synonyms

1. Raplon

2. 156137-99-4

3. Org 9487

4. Org-9487

5. 156137-99-4 (bromide)

6. 65q4qdg4kc

7. 1-((2s,3s,5s,8r,9s,10s,13s,14s,16s,17r)-3-acetoxy-10,13-dimethyl-2-(piperidin-1-yl)-17-(propionyloxy)hexadecahydro-1h-cyclopenta[a]phenanthren-16-yl)-1-allylpiperidin-1-ium Bromide

8. Raplon (tn)

9. Ncgc00183839-01

10. Unii-65q4qdg4kc

11. Rapacuronium Bromide [usan:inn:ban]

12. Dsstox_cid_28749

13. Dsstox_rid_83018

14. Dsstox_gsid_48823

15. Schembl41132

16. 1-(3alpha-acetoxy-2beta-(1-piperidinyl)-17beta-(propionyloxy)-5alpha-androsta-16beta-yl)-1-allylpiperidinium Bromide

17. Chembl1200549

18. Dtxsid7048823

19. Rapacuronium Bromide [mi]

20. Rapacuronium Bromide (usan/inn)

21. Rapacuronium Bromide [inn]

22. Rapacuronium Bromide [usan]

23. Rapacuronium Bromide [vandf]

24. Tox21_113304

25. Rapacuronium Bromide [mart.]

26. Rapacuronium Bromide [who-dd]

27. Cs-6564

28. 1-allyl-1-(3alpha,17beta-dihydroxy-2beta-piperidino-5alpha-androstan-16beta-yl)piperidinium Bromide, 3-acetate 17-propionate

29. Hy-16423

30. Piperidinium, 1-((2beta,3alpha,5alpha,16beta,17beta)-3-(acetyloxy)-17-(1-oxopropoxy)-2-(1-piperidinyl)androstan-16-yl)-1-(2-propenyl)-, Bromide

31. Rapacuronium Bromide [orange Book]

32. Cas-156137-99-4

33. D05703

34. Q3419354

35. [(2s,3s,5s,8r,9s,10s,13s,14s,16s,17r)-3-acetyloxy-10,13-dimethyl-2-piperidin-1-yl-16-(1-prop-2-enylpiperidin-1-ium-1-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl] Propanoate;bromide

36. 1-allyl-1-(3.alpha.,17.beta.-dihydroxy-2.beta.-piperidino-5.alpha.-androstan-16.beta.-yl)piperidinium Bromide, 3-acetate 17-propionate

2.4 Create Date
2005-12-16
3 Chemical and Physical Properties
Molecular Weight 677.8 g/mol
Molecular Formula C37H61BrN2O4
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count6
Rotatable Bond Count9
Exact Mass676.38147 g/mol
Monoisotopic Mass676.38147 g/mol
Topological Polar Surface Area55.8 Ų
Heavy Atom Count44
Formal Charge0
Complexity1030
Isotope Atom Count0
Defined Atom Stereocenter Count10
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Pharmacology and Biochemistry
4.1 MeSH Pharmacological Classification

Neuromuscular Nondepolarizing Agents

Drugs that interrupt transmission at the skeletal neuromuscular junction without causing depolarization of the motor end plate. They prevent acetylcholine from triggering muscle contraction and are used as muscle relaxants during electroshock treatments, in convulsive states, and as anesthesia adjuvants. (See all compounds classified as Neuromuscular Nondepolarizing Agents.)


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