Record Information |
---|
Version | 2.0 |
---|
Created at | 2022-09-12 09:44:29 UTC |
---|
Updated at | 2022-09-12 09:44:29 UTC |
---|
NP-MRD ID | NP0327290 |
---|
Secondary Accession Numbers | None |
---|
Natural Product Identification |
---|
Common Name | (1r,3ar,5as,7s,9ar,9bs,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(1z)-5-methyl-4-methylidenehex-1-en-1-yl]-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol |
---|
Description | Abscisterol F belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans. (1r,3ar,5as,7s,9ar,9bs,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(1z)-5-methyl-4-methylidenehex-1-en-1-yl]-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol is found in Pezicula livida. It was first documented in 2022 (PMID: 36130709). Based on a literature review a significant number of articles have been published on Abscisterol F (PMID: 36130592) (PMID: 36130585) (PMID: 36130517) (PMID: 36130480). |
---|
Structure | CC(C)C(=C)C\C=C/[C@H]1CC[C@H]2C3=CC[C@H]4C[C@@H](O)CC[C@]4(CO)[C@H]3CC[C@]12C InChI=1S/C27H42O2/c1-18(2)19(3)6-5-7-20-9-11-24-23-10-8-21-16-22(29)12-15-27(21,17-28)25(23)13-14-26(20,24)4/h5,7,10,18,20-22,24-25,28-29H,3,6,8-9,11-17H2,1-2,4H3/b7-5-/t20-,21-,22-,24-,25-,26+,27+/m0/s1 |
---|
Synonyms | Not Available |
---|
Chemical Formula | C27H42O2 |
---|
Average Mass | 398.6310 Da |
---|
Monoisotopic Mass | 398.31848 Da |
---|
IUPAC Name | (1S,2R,5S,7S,11R,14R,15R)-2-(hydroxymethyl)-15-methyl-14-[(1Z)-5-methyl-4-methylidenehex-1-en-1-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-5-ol |
---|
Traditional Name | (1S,2R,5S,7S,11R,14R,15R)-2-(hydroxymethyl)-15-methyl-14-[(1Z)-5-methyl-4-methylidenehex-1-en-1-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-5-ol |
---|
CAS Registry Number | Not Available |
---|
SMILES | CC(C)C(=C)C\C=C/[C@H]1CC[C@H]2C3=CC[C@H]4C[C@@H](O)CC[C@]4(CO)[C@H]3CC[C@]12C |
---|
InChI Identifier | InChI=1S/C27H42O2/c1-18(2)19(3)6-5-7-20-9-11-24-23-10-8-21-16-22(29)12-15-27(21,17-28)25(23)13-14-26(20,24)4/h5,7,10,18,20-22,24-25,28-29H,3,6,8-9,11-17H2,1-2,4H3/b7-5-/t20-,21-,22-,24-,25-,26+,27+/m0/s1 |
---|
InChI Key | MGUPDIUDFLRFKN-CZJUOIDJSA-N |
---|
Experimental Spectra |
---|
|
| Not Available | Predicted Spectra |
---|
|
| Spectrum Type | Description | Depositor ID | Depositor Organization | Depositor | Deposition Date | View |
---|
1D NMR | 13C NMR Spectrum (1D, 25 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 100 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 252 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 1000 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 50 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 200 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 75 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 300 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 101 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 400 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 126 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 500 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 151 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 600 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 176 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 700 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 201 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 800 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 226 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 900 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum |
| Chemical Shift Submissions |
---|
|
| Not Available | Species |
---|
Species of Origin | |
---|
Chemical Taxonomy |
---|
Description | Belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans. |
---|
Kingdom | Organic compounds |
---|
Super Class | Lipids and lipid-like molecules |
---|
Class | Steroids and steroid derivatives |
---|
Sub Class | Androstane steroids |
---|
Direct Parent | Androgens and derivatives |
---|
Alternative Parents | |
---|
Substituents | - 19-hydroxysteroid
- Androgen-skeleton
- 3-beta-hydroxysteroid
- Hydroxysteroid
- 3-hydroxysteroid
- 3-hydroxy-delta-7-steroid
- Delta-7-steroid
- Cyclic alcohol
- Secondary alcohol
- Organic oxygen compound
- Hydrocarbon derivative
- Primary alcohol
- Organooxygen compound
- Alcohol
- Aliphatic homopolycyclic compound
|
---|
Molecular Framework | Aliphatic homopolycyclic compounds |
---|
External Descriptors | Not Available |
---|
Physical Properties |
---|
State | Not Available |
---|
Experimental Properties | Property | Value | Reference |
---|
Melting Point | Not Available | Not Available | Boiling Point | Not Available | Not Available | Water Solubility | Not Available | Not Available | LogP | Not Available | Not Available |
|
---|
Predicted Properties | |
---|
General References | - Slowing K, Gomez F, Delgado M, Fernandez de la Rosa R, Hernandez-Martin N, Pozo MA, Garcia-Garcia L: PET Imaging and Neurohistochemistry Reveal that Curcumin Attenuates Brain Hypometabolism and Hippocampal Damage induced by Status Epilepticus in Rats. Planta Med. 2022 Sep 21. doi: 10.1055/a-1948-4378. [PubMed:36130709 ]
- Ye L, Wang X, McFarland A, Madsen JJ: (19)F NMR: A promising tool for dynamic conformational studies of G protein-coupled receptors. Structure. 2022 Sep 7. pii: S0969-2126(22)00351-3. doi: 10.1016/j.str.2022.08.007. [PubMed:36130592 ]
- Terheyden JH, Finger RP, Wicharz F, Herrmann P, Holz FG, Tufail A, Muller PL: Properties of patient-reported outcome measures in recessive Stargardt disease. Ophthalmologica. 2022 Sep 21. pii: 000527093. doi: 10.1159/000527093. [PubMed:36130585 ]
- Rush SA, Brar G, Hsieh CL, Chautard E, Rainho-Tomko JN, Slade CD, Bricault CA, Kume A, Kearns J, Groppo R, Mundle ST, Zhang L, Casimiro D, Fu TM, DiNapoli JM, McLellan JS: Characterization of prefusion-F-specific antibodies elicited by natural infection with human metapneumovirus. Cell Rep. 2022 Sep 20;40(12):111399. doi: 10.1016/j.celrep.2022.111399. [PubMed:36130517 ]
- Richard G, Blondin DP, Syed SA, Rossi L, Fontes ME, Fortin M, Phoenix S, Frisch F, Dubreuil S, Guerin B, Turcotte EE, Lepage M, Surette MG, Schertzer JD, Steinberg GR, Morrison KM, Carpentier AC: High-fructose feeding suppresses cold-stimulated brown adipose tissue glucose uptake independently of changes in thermogenesis and the gut microbiome. Cell Rep Med. 2022 Sep 20;3(9):100742. doi: 10.1016/j.xcrm.2022.100742. [PubMed:36130480 ]
- LOTUS database [Link]
|
---|