DR ANTHONY MELVIN CRASTO,WorldDrugTracker, helping millions, A 90 % paralysed man in action for you, I am suffering from transverse mylitis and bound to a wheel chair, With death on the horizon, nothing will not stop me except God................DR ANTHONY MELVIN CRASTO Ph.D ( ICT, Mumbai) , INDIA 25Yrs Exp. in the feld of Organic Chemistry,Working for GLENMARK GENERICS at Navi Mumbai, INDIA. Serving chemists around the world. Helping them with websites on Chemistry.Million hits on google, world acclamation from industry, academia, drug authorities for websites, blogs and educational contribution

Thursday 23 April 2015

LOMITAPIDE MESYLATE NMR PREDICTIONS


methanesulfonic acid,N-(2,2,2-trifluoroethyl)-9-[4-[4-[[2-[4-(trifluoromethyl)phenyl]benzoyl]amino]piperidin-1-yl]butyl]fluorene-9-carboxamide

LOMITAPIDE MESYLATE

Methanesulfonic acid,N-(2,2,2-trifluoroethyl)-9-[4-[4-[[2-[4-(trifluoromethyl)phenyl]benzoyl]amino]piperidin-1-yl]butyl]fluorene-9-carboxamide
CAS No.:202914-84-9
Synonyms:
  • Juxtapid;
  • UNII-X4S83CP54E;
  • Lomitapide mesylate;
  • AEGR-733;
Formula:C40H41F6N3O5S
Exact Mass:789.26700



Lomitapide mesylate is a white to off-white powder that is slightly
soluble in aqueous solutions of pH 2 to 5. Lomitapide mesylate is freely soluble in acetone,ethanol and methanol; soluble in 2-butanol, methylene chloride andacetonitrile; sparingly soluble in 1-octanol and 2-propanol; slightly soluble in ethyl acetate; and insoluble in heptane.........https://www.cadth.ca/sites/default/files/cdr/monograph/Juxtapid_Product%20Monograph.pdf

他哌( INN,作为Juxtapid销售在美国和欧盟Lojuxta )是治疗家族性高胆固醇血症药物,由Aegerion药品开发。 它已作为单一治疗进行临床试验和与阿托伐他汀的复方,依泽替米贝和非诺贝特。 美国食品和药物管理局( fda ) 2012年12月21日批准了他哌,孤儿药物以降低LDL胆固醇、总胆固醇、载脂蛋白B,和乘坐吊盘上下密度脂蛋白(非HDL )胆固醇在同合子家族性高胆固醇血症患者( HoFH )。 2013年5月31日,欧洲人用医药产品委员会( CHMP )一个积极的意见,一致表决通过推荐营销授权他哌。 2013年7月31日,欧洲委员会批准他哌作为一个低脂肪饮食和其它降脂药物产品有或没有低密度脂蛋白( ldl )机在HoFH成年患者。


SEE NMR GIVEN BY MEDKOO
http://www.medkoo.com/Product-Data/LomitapideMesylate/QC-LomitapideMesylate-BBC41017web.pdf

Juxtapid (lomitapide) is developed and manufactured by Aegerion Pharmaceuticals for the treatment of patients with homozygous familial hypercholesterolemia (HoFH).
In December 2012, the US Food and Drug Administration (FDA) approved Juxtapid for lipoprotein cholesterol reduction in HoFH patients.

Lomitapide (Juxtapid® and Lojuxta®; Aegerion Pharmaceuticals, Inc., MA, USA), an orally administered inhibitor of the microsomal triglyceride transfer protein, inhibits the synthesis and secretion of ApoB-containing lipoproteins and, thus, reduces plasma levels of LDL cholesterol (LDL-C). Lomitapide has been approved for the therapy of homozygous familial hypercholesterolemia patients.

Homozygous Familial Hypercholesterolemia (HoFH)

"In December 2012, the US Food and Drug Administration approved Juxtapid for lipoprotein cholesterol reduction in HoFH patients."
HoFH is an uncommon genetic disease that impairs the function of the receptor responsible for removing lipoprotein cholesterol (LDL-C) and total cholesterol from the body. The disease is inherited from parents and is characterised by high levels of LDL cholesterol. It results in developing premature and progressive atherosclerosis by narrowing or blocking of the arteries.
The disease is found in about one out of 1,000,000 persons internationally.

Juxtapid's mechanism of action

Juxtapid contains lomitapide, which inhibits the microsomal triglyceride transfer protein (MTTP). The MTTP is an important gene that is necessary for low-density lipoprotein (VLDL) assembly and secretion in the liver. The drug is available in capsule form for oral administration.

1H NMR PREDICT OF MESYLATE
methanesulfonic acid,N-(2,2,2-trifluoroethyl)-9-[4-[4-[[2-[4-(trifluoromethyl)phenyl]benzoyl]amino]piperidin-1-yl]butyl]fluorene-9-carboxamide NMR spectra analysis, Chemical CAS NO. 202914-84-9 NMR spectral analysis, methanesulfonic acid,N-(2,2,2-trifluoroethyl)-9-[4-[4-[[2-[4-(trifluoromethyl)phenyl]benzoyl]amino]piperidin-1-yl]butyl]fluorene-9-carboxamide H-NMR spectrum
13 C NMR PREDICT OF MESYLATE

methanesulfonic acid,N-(2,2,2-trifluoroethyl)-9-[4-[4-[[2-[4-(trifluoromethyl)phenyl]benzoyl]amino]piperidin-1-yl]butyl]fluorene-9-carboxamide NMR spectra analysis, Chemical CAS NO. 202914-84-9 NMR spectral analysis, methanesulfonic acid,N-(2,2,2-trifluoroethyl)-9-[4-[4-[[2-[4-(trifluoromethyl)phenyl]benzoyl]amino]piperidin-1-yl]butyl]fluorene-9-carboxamide C-NMR spectrum

COSY PREDICT


HMBC ABOVE
............


LOMITAPIDE FREE BASE


1H NMR PREDICT
N-(2,2,2-trifluoroethyl)-9-[4-[4-[[2-[4-(trifluoromethyl)phenyl]benzoyl]amino]piperidin-1-yl]butyl]fluorene-9-carboxamide NMR spectra analysis, Chemical CAS NO. 182431-12-5 NMR spectral analysis, N-(2,2,2-trifluoroethyl)-9-[4-[4-[[2-[4-(trifluoromethyl)phenyl]benzoyl]amino]piperidin-1-yl]butyl]fluorene-9-carboxamide H-NMR spectrum


13C PREDICT OF BASE
N-(2,2,2-trifluoroethyl)-9-[4-[4-[[2-[4-(trifluoromethyl)phenyl]benzoyl]amino]piperidin-1-yl]butyl]fluorene-9-carboxamide NMR spectra analysis, Chemical CAS NO. 182431-12-5 NMR spectral analysis, N-(2,2,2-trifluoroethyl)-9-[4-[4-[[2-[4-(trifluoromethyl)phenyl]benzoyl]amino]piperidin-1-yl]butyl]fluorene-9-carboxamide C-NMR spectrum





Structure:


Spectrum Plot:

Max ppm:
Min ppm:
Number of points:
Line width (Hz):
Annotate shifts:
Display integral:

 Cite:

R.J. Abraham, M. Mobli Modelling 1H NMR Spectra of Organic Compounds: Theory, Applications and NMR Prediction Software, Wiley, Chichester, 2008.

Shifts:

Index Name Shift (ppm)
6 H28 4.172
7 H29 4.172
9 H23 6.800
15 H1 2.647
16 H2 2.647
19 H19 7.546
21 H25 7.479
24 H22 7.809
26 H27 7.567
29 H21 7.809
31 H26 7.567
33 H24 7.479
35 H18 7.546
37 H3 1.059
38 H4 1.059
40 H6 1.677
41 H7 1.677
43 H8 2.163
44 H9 2.163
47 H10 2.264
48 H11 2.264
50 H14 1.554
51 H15 1.554
53 H5 2.607
55 H20 5.687
60 H30 7.438
62 H32 7.422
64 H33 7.542
66 H31 7.781
70 H34 8.175
72 H36 7.663
75 H37 7.663
77 H35 8.175
83 H12 2.264
84 H13 2.264
86 H16 1.554
87 H17 1.554

Couplings:

Index 1 Index 2 Coupling (Hz)
1 3 160.00
1 4 160.00
1 6 9.58
1 7 9.58
3 4 160.00
3 6 9.58
3 7 9.58
4 6 9.58
4 7 9.58
6 7 -12.50
6 9 2.56
7 9 7.98
15 16 -13.20
15 37 2.51
15 38 13.21
16 37 13.21
16 38 2.65
19 21 7.50
19 24 0.60
19 26 1.10
21 24 1.10
21 26 7.50
24 26 7.50
24 29 0.60
29 31 7.50
29 33 1.10
29 35 0.60
31 33 7.50
31 35 1.10
33 35 7.50
37 38 -13.20
37 40 13.20
37 41 2.87
38 40 2.31
38 41 13.20
40 41 -13.20
40 43 12.59
40 44 4.04
41 43 1.83
41 44 12.21
43 44 -12.50
47 48 -12.50
47 50 1.85
47 51 4.26
47 53 0.56
48 50 3.45
48 51 12.43
48 53 -0.30
50 51 -13.20
50 53 2.58
50 86 0.48
50 87 1.29
51 53 11.93
51 86 -0.32
51 87 0.49
53 55 7.67
53 83 -0.31
53 84 0.55
53 86 11.93
53 87 2.57
60 62 7.50
60 64 1.10
60 66 0.60
62 64 7.50
62 66 1.10
64 66 7.50
66 70 0.60
66 77 0.60
70 72 7.50
70 75 0.60
70 77 1.90
72 75 1.90
72 77 0.60
72 79 -1.50
72 80 -1.50
72 81 -1.50
75 77 7.50
75 79 -1.50
75 80 -1.50
75 81 -1.50
79 80 160.00
79 81 160.00
80 81 160.00
83 84 -12.50
83 86 12.41
83 87 3.48
84 86 4.33
84 87 1.82
86 87 -13.20
 


 http://www.pharmadl.com/stmt-show_2babd0fa-723a-427d-96fe-cad4e2903f00_aeea1ded-3186-4f50-982f-01efab0779cc.html



Lomitapide

Common name: Lomitapide; AEGR 733; AEGR-733; BMS 201038; BMS-201038; Juxtapid; Lojuxta; Lomitapide Mesylate
Trademarks: Juxtapid; Lojuxta
Molecular Formula: C39H37F6N3O2
CAS Registry Number: 182431-12-5; 202914-84-9 (Mesylate)
CAS Name: N-(2,2,2-trifluoroethyl)-9-[4-(4-{2-[4-(trifluoromethyl)phenyl]benzamido}piperidin-1-yl)butyl]-9H-fluorene-9-carboxamide
Molecular Weight: 693.720
SMILES:C1CN(CCC1NC(=O)C2=CC=CC=C2C3=CC=C(C=C3)C(F)(F)F)CCCCC4(C5=CC=CC=C5C6=CC=CC=C64)C(=O)NCC(F)(F)F
InChI Key: MBBCVAKAJPKAKM-UHFFFAOYSA-N
InChI: InChI=1S/C39H37F6N3O2/c40-38(41,42)25-46-36(50)37(33-13-5-3-10-30(33)31-11-4-6-14-34(31)37)21-7-8-22-48-23-19-28(20-24-48)47-35(49)32-12-2-1-9-29(32)26-15-17-27(18-16-26)39(43,44)45/h1-6,9-18,28H,7-8,19-25H2,(H,46,50)(H,47,49)
Activity: Treatment of Familial Hypercholesterolemia; Microsomal Triglyceride Transfer Protein Inhibitor; MTP Inhibitor; Cholesterol Lowering Drug; Hypolipidemic Agents
Status: Launched 2012 (US); 2013 (EU)
Originator: Aegerion Pharmaceuticals Inc




NASIK INDIA
Map of nasik








Image result for NASIK





Pandavleni_Caves_near_Nasik





Nashik Ganga Ghat, Panchwati, Nasik, Maharashtra - India | 





P.S. : The views expressed are my personal and in no-way suggest the views of the professional body or the company that I represent.
P.S. : The views expressed are my personal and in no-way suggest the views of the professional body or the company that I represent.
P.S. : The views expressed are my personal and in no-way suggest the views of the professional body or the company that I represent.





COCK WILL TEACH YOU NMR



COCK SAYS MOM CAN TEACH YOU NMR


DRUG APPROVALS BY DR ANTHONY MELVIN CRASTO .....FOR BLOG HOME CLICK HERE

Join me on Linkedin

View Anthony Melvin Crasto Ph.D's profile on LinkedIn

Join me on Facebook FACEBOOK
Join me on twitterFollow amcrasto on Twitter     
Join me on google plus Googleplus

         

 amcrasto@gmail.com

No comments:

Post a Comment