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Details
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This molecule with other stereoconfigurations:
Molecule | 60005373 |
Chemical name(s) | strongylophorine-22
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Chemical formula | C26H38O2 |
Molecular weight | 382.58 |
Number of double bond equivalents (DBEs) | 8.0 |
Number of all rings, size of smallest set of smallest rings | 15, 5 |
Canonical name(s) |
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CAS-Number |
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Additional information |
Links from Unichem:
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Molecule keywords | |
DOI | |
1H Spectrum | 60006214
Rating: 10 (10: 10: nmrshiftdb2 quality check: accept/reliability: excellent (admin)) |
Type | 1H |
Measurement conditions
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Temperature [K] | 298 |
Solvent | Chloroform-D1 (CDCl3) |
Field Strength [MHz] | 500.0 |
Assignment Method | COSY,HMBC,HMQC,NOESY |
Literature |
Yasuji Yamada; Rob W. M. van Soest; Ayako Hoshino; Akinori Shintani; Hidemichi Mitome; Hiroaki Miyaoka: New Strongylophorines from the Okinawan Marine Sponge Petrosia (Strongylophora) corticata, in: Journal of Natural Products, vol. 66/2003, pp. 1600 - 1605 (DOI: 10.1021/np030312q).
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Additional comments | |
nmrshiftdb2 quality report |
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Additional information |
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Spectrum categories | |
Type: 13C 125.0 Double click to get resizeable window!
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Atom |
Mult.(coupling const.) |
Meas. Shift |
1
|
T |
39.9 |
2
|
T |
18.6 |
3
|
T |
42.1 |
4
|
S |
33.3 |
5
|
D |
56.5 |
6
|
S |
37.5 |
7
|
T |
18.2 |
8
|
T |
41.0 |
9
|
S |
37.1 |
10
|
D |
60.7 |
11
|
D |
52.4 |
12
|
S |
76.6 |
13
|
T |
41.1 |
14
|
T |
18.6 |
15
|
T |
22.4 |
16
|
S |
123.3 |
17
|
S |
147.2 |
19
|
D |
115.8 |
20
|
S |
148.5 |
21
|
D |
114.2 |
22
|
D |
117.5 |
24
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Q |
20.5 |
25
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Q |
16.0 |
26
|
Q |
16.4 |
27
|
S |
33.3 |
28
|
Q |
21.4 |
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