1,2-DICAPRYL-SN-GLYCERO-3-PHOSPHOCHOLINE — Substances (GSRS)

Codes

Uuid
95500265-329a-403f-af07-75e78cdebbdc
Code
3436-44-0
Type
PRIMARY
Url
https://commonchemistry.cas.org/detail?cas_rn=3436-44-0
Code system
CAS
References
4e706f88-69ee-410a-8444-fe35167dabdb, 578c7cbe-0553-4e2d-b50d-c8829e11c00e
Uuid
af8b72fc-8123-42ab-8f1b-6794308746f0
Code
C015132
Type
PRIMARY
Url
http://www.ncbi.nlm.nih.gov/mesh/67015132
Code system
MESH
References
4e706f88-69ee-410a-8444-fe35167dabdb
Uuid
bdccb20b-42fa-4fff-9849-9715288a3b5c
Code
16219892
Type
PRIMARY
Url
https://pubchem.ncbi.nlm.nih.gov/compound/16219892
Code system
PUBCHEM
References
4e706f88-69ee-410a-8444-fe35167dabdb
Uuid
d7e68fd3-d867-447b-a5cf-6576ea1e178d
Code
66BXC7TK3J
Type
PRIMARY
Code system
FDA UNII
Uuid
5870973a-ecc4-2241-7126-cfba03cb5cad
Code
78226
Type
PRIMARY
Url
https://www.ebi.ac.uk/chebi/chebiOntology.do?chebiId=CHEBI:78226
Code system
CHEBI
References
71477ba9-3629-3257-8cad-81cff44149ed
Uuid
f6f8b6ad-fa40-0b63-92b5-a8b608b4f8bc
Code
DTXSID801033927
Type
PRIMARY
Url
https://comptox.epa.gov/dashboard/chemical/details/DTXSID801033927
Code system
EPA CompTox
References
71477ba9-3629-3257-8cad-81cff44149ed

Names

Uuid
337cd721-b623-489a-934f-7d68cec8436e
Name
1,2-DICAPRYL-SN-GLYCERO-3-PHOSPHOCHOLINE
StdName
1,2-DICAPRYL-SN-GLYCERO-3-PHOSPHOCHOLINE
Type
cn
Preferred
false
Display name
false
Languages
en
References
3ba8b0c9-1d3d-462f-a77f-822a4aada75f
Uuid
2233ceab-ba2d-4ac5-88af-6c2786f98a6e
Name
1,2-DIDECANOYL-PHOSPHATIDYLCHOLINE, R-
StdName
1,2-DIDECANOYL-PHOSPHATIDYLCHOLINE, R-
Type
cn
Preferred
false
Display name
false
Languages
en
References
e68e2e8d-ea22-4c16-9856-89f18963695f
Uuid
48d666a5-af34-40b0-bddf-db43934c1146
Name
1,2-DIDECANOYL-SN-GLYCERO-3-PHOSPHOCHOLINE
StdName
1,2-DIDECANOYL-SN-GLYCERO-3-PHOSPHOCHOLINE
Type
cn
Preferred
false
Display name
true
Languages
en
References
cf4acdc1-89ca-457c-a88a-67e7e70416b6
Uuid
d83d26ff-d10e-45c5-a59c-4d14fb1436a1
Name
10:0 PC, R-
StdName
10:0 PC, R-
Type
cn
Preferred
false
Display name
false
Languages
en
References
63dbfc36-a449-4c8e-b114-3e78eb9c6bf9
Uuid
32a03635-c8c9-46f1-99cd-b222b02b3fbb
Name
3,5,9-TRIOXA-4-PHOSPHANONADECAN-1-AMINIUM, 4-HYDROXY-N,N,N-TRIMETHYL-10-OXO-7-((1-OXODECYL)OXY)-, INNER SALT, 4-OXIDE, (7R)-
StdName
3,5,9-TRIOXA-4-PHOSPHANONADECAN-1-AMINIUM, 4-HYDROXY-N,N,N-TRIMETHYL-10-OXO-7-((1-OXODECYL)OXY)-, INNER SALT, 4-OXIDE, (7R)-
Type
cn
Preferred
false
Display name
false
Languages
en
References
cf4acdc1-89ca-457c-a88a-67e7e70416b6
Uuid
20f9acde-4ba3-4aba-974e-010bbc222f5b
Name
DCPC, L
StdName
DCPC, L
Type
cn
Preferred
false
Display name
false
Languages
en
References
3ba8b0c9-1d3d-462f-a77f-822a4aada75f
Uuid
b9706368-9e17-42cd-becf-824572cedcae
Name
DDPC, L-
StdName
DDPC, L-
Type
cn
Preferred
false
Display name
false
Languages
en
References
e68e2e8d-ea22-4c16-9856-89f18963695f
Uuid
32863ff0-d6fb-46a5-ae79-d88414386b70
Name
DDPC, R-
StdName
DDPC, R-
Type
cn
Preferred
false
Display name
false
Languages
en
References
e68e2e8d-ea22-4c16-9856-89f18963695f
Uuid
1c923135-a5cf-4186-b66f-71f547fc0028
Name
DIC10:0 PC
StdName
DIC10:0 PC
Type
cd
Preferred
false
Display name
false
Languages
en
References
3ba8b0c9-1d3d-462f-a77f-822a4aada75f
Uuid
b579d89d-6080-4b56-9254-83ecac3d89b5
Name
DIDECANOYL-L-.ALPHA.-PHOSPHATIDYLCHOLINE
StdName
DIDECANOYL-L-.ALPHA.-PHOSPHATIDYLCHOLINE
Type
cn
Preferred
false
Display name
false
Languages
en
References
49c022a7-701b-43b1-ab09-0e97f0e3cc0d
Uuid
6751b7d5-c80d-4088-9213-aa2e516a8673
Name
L-DICAPRYLLECITHIN
StdName
L-DICAPRYLLECITHIN
Type
cn
Preferred
false
Display name
false
Languages
en
References
94291e9e-e04c-4b20-a5a3-bc0e7e5bbd07
Uuid
97870804-b4ec-4fb8-a5a9-9a4f4c2f6ed2
Name
L-DIDECANOYLPHOSPHATIDYLCHOLINE
StdName
L-DIDECANOYLPHOSPHATIDYLCHOLINE
Type
cn
Preferred
false
Display name
false
Languages
en
References
94291e9e-e04c-4b20-a5a3-bc0e7e5bbd07

References

Uuid
63dbfc36-a449-4c8e-b114-3e78eb9c6bf9
Citation
FDA_SRS
Doc type
SRS
Public domain
true
Tags
NOMEN, PUBLIC_DOMAIN_RELEASE, AUTO_SELECTED
Uuid
cf4acdc1-89ca-457c-a88a-67e7e70416b6
Citation
STN
Doc type
SRS
Public domain
true
Tags
NOMEN
Uuid
e68e2e8d-ea22-4c16-9856-89f18963695f
Citation
fda_srs
Doc type
SRS
Public domain
true
Tags
NOMEN
Uuid
94291e9e-e04c-4b20-a5a3-bc0e7e5bbd07
Citation
stn
Doc type
SRS
Public domain
true
Tags
NOMEN
Uuid
49c022a7-701b-43b1-ab09-0e97f0e3cc0d
Citation
chemid
Doc type
SRS
Public domain
true
Tags
NOMEN
Uuid
3ba8b0c9-1d3d-462f-a77f-822a4aada75f
Citation
http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T1T-4MXJ3TN-3&_user=861681&_coverDate=05%
Url
http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T1T-4MXJ3TN-3&_user=861681&_coverDate=05%
Doc type
SRS
Public domain
true
Tags
NOMEN
Uuid
4e706f88-69ee-410a-8444-fe35167dabdb
Citation
SRS CODE IMPORT
Doc type
SRS
Public domain
true
Document date
1493390561000
Tags
NOMEN
Uuid
8a6ae4a9-d5e1-459c-8a2c-03189a8bdc40
Citation
SRS import [66BXC7TK3J]
Url
http://fdasis.nlm.nih.gov/srs/srsdirect.jsp?regno=66BXC7TK3J
Doc type
SRS
Public domain
true
Document date
1493390561000
Tags
NOMEN
Uuid
71477ba9-3629-3257-8cad-81cff44149ed
Doc type
SYSTEM
Public domain
true
Uuid
578c7cbe-0553-4e2d-b50d-c8829e11c00e
Citation
STN
Doc type
STN (SCIFINDER)
Public domain
true

Moieties

Uuid
8af61745-4c6a-4717-88ee-b642a17dadeb
ID
8af61745-4c6a-4717-88ee-b642a17dadeb
Smiles
CCCCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCCC
Formula
C28H56NO8P
Atropisomerism
No
Charge
0
Count
1
Stereochemistry
EPIMERIC
Defined stereo
1
Ez centers
0
Molecular weight
565.721
Optical activity
UNSPECIFIED
Stereo centers
1
Molfile
Marvin 01132107132D 38 37 0 0 1 0 999 V2000 7.3885 -3.9017 0.0000 C 0 0 2 0 0 0 0 0 0 1 0 0 6.6637 -3.5078 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9601 -3.9386 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 5.2352 -3.5447 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.2139 -2.7200 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 4.5316 -3.9755 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.8068 -3.5817 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1032 -4.0124 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3782 -3.6186 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.6746 -4.0494 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9498 -3.6554 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.2462 -4.0863 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.4787 -3.6923 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.1823 -4.1232 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.0921 -3.4709 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.8171 -3.8649 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.5207 -3.4340 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0 10.1388 -2.8875 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0 9.0301 -2.7707 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.1189 -4.0022 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.9100 -3.7681 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.5083 -4.3362 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.2994 -4.1022 0.0000 N 0 3 0 0 0 0 0 0 0 3 0 0 12.7302 -4.8058 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.0378 -3.7342 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.9973 -3.3344 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.4273 -4.9166 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6.7084 -5.3214 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.6995 -6.1464 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 5.9984 -4.9012 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.2795 -5.3060 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.5696 -4.8858 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.8506 -5.2906 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1407 -4.8704 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4218 -5.2752 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.7117 -4.8549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9929 -5.2598 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.2829 -4.8396 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 0 0 0 1 15 1 0 0 0 0 1 27 1 6 0 0 0 3 2 1 0 0 0 0 4 3 1 0 0 0 0 4 5 2 0 0 0 0 6 4 1 0 0 0 0 7 6 1 0 0 0 0 8 7 1 0 0 0 0 9 8 1 0 0 0 0 10 9 1 0 0 0 0 11 10 1 0 0 0 0 12 11 1 0 0 0 0 13 12 1 0 0 0 0 14 13 1 0 0 0 0 15 16 1 0 0 0 0 16 17 1 0 0 0 0 17 18 1 0 0 0 0 17 19 2 0 0 0 0 17 20 1 0 0 0 0 20 21 1 0 0 0 0 21 22 1 0 0 0 0 22 23 1 0 0 0 0 23 24 1 0 0 0 0 23 25 1 0 0 0 0 23 26 1 0 0 0 0 27 28 1 0 0 0 0 28 29 2 0 0 0 0 28 30 1 0 0 0 0 30 31 1 0 0 0 0 31 32 1 0 0 0 0 32 33 1 0 0 0 0 33 34 1 0 0 0 0 34 35 1 0 0 0 0 35 36 1 0 0 0 0 36 37 1 0 0 0 0 37 38 1 0 0 0 0 M CHG 2 18 -1 23 1 M END
Count amount
Type
MOL RATIO
Average
1
Units
MOL RATIO
Uuid
30843b8c-900e-48eb-afec-1f5b5d4184b7

Structure

ID: 8e06695e-3b84-4822-ab3b-25f2fc3430cd
Smiles: CCCCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCCC
Formula: C28H56NO8P
Atropisomerism: No
Charge: 0
Count: 1
Stereochemistry: ABSOLUTE
Defined stereo: 1
Ez centers: 0
Molecular weight: 565.721
Optical activity: UNSPECIFIED
Stereo centers: 1
Molfile: Marvin 01132107222D 38 37 0 0 1 0 999 V2000 5.2139 -2.7200 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 5.2352 -3.5447 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9601 -3.9386 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6.6637 -3.5078 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.3885 -3.9017 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 8.0921 -3.4709 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.8171 -3.8649 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.5207 -3.4340 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0 10.1388 -2.8875 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0 9.0301 -2.7707 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.1189 -4.0022 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.9100 -3.7681 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.5083 -4.3362 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.2994 -4.1022 0.0000 N 0 3 0 0 0 0 0 0 0 0 0 0 12.7302 -4.8058 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.0378 -3.7342 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.9973 -3.3344 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.4273 -4.9166 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6.7084 -5.3214 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.6995 -6.1464 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 5.9984 -4.9012 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.2795 -5.3060 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.5696 -4.8858 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.8506 -5.2906 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1407 -4.8704 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4218 -5.2752 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.7117 -4.8549 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9929 -5.2598 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.2829 -4.8396 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.5316 -3.9755 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.8068 -3.5817 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1032 -4.0124 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3782 -3.6186 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.6746 -4.0494 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9498 -3.6554 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.2462 -4.0863 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.4787 -3.6923 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.1823 -4.1232 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2 1 2 0 0 0 0 2 3 1 0 0 0 0 3 4 1 0 0 0 0 5 4 1 0 0 0 0 5 6 1 0 0 0 0 6 7 1 0 0 0 0 7 8 1 0 0 0 0 8 9 1 0 0 0 0 8 10 2 0 0 0 0 8 11 1 0 0 0 0 11 12 1 0 0 0 0 12 13 1 0 0 0 0 13 14 1 0 0 0 0 14 15 1 0 0 0 0 14 16 1 0 0 0 0 14 17 1 0 0 0 0 5 18 1 6 0 0 0 18 19 1 0 0 0 0 19 20 2 0 0 0 0 19 21 1 0 0 0 0 21 22 1 0 0 0 0 22 23 1 0 0 0 0 23 24 1 0 0 0 0 24 25 1 0 0 0 0 25 26 1 0 0 0 0 26 27 1 0 0 0 0 27 28 1 0 0 0 0 28 29 1 0 0 0 0 30 2 1 0 0 0 0 31 30 1 0 0 0 0 32 31 1 0 0 0 0 33 32 1 0 0 0 0 34 33 1 0 0 0 0 35 34 1 0 0 0 0 36 35 1 0 0 0 0 37 36 1 0 0 0 0 38 37 1 0 0 0 0 M CHG 2 9 -1 14 1 M END
References: cf4acdc1-89ca-457c-a88a-67e7e70416b6, 8a6ae4a9-d5e1-459c-8a2c-03189a8bdc40