Record Information |
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Version | 5.0 |
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Status | Expected but not Quantified |
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Creation Date | 2012-09-11 19:59:10 UTC |
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Update Date | 2022-03-07 02:54:20 UTC |
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HMDB ID | HMDB0035046 |
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Secondary Accession Numbers | |
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Metabolite Identification |
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Common Name | Gibberellin A43 |
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Description | Gibberellin A43, also known as GA43, belongs to the class of organic compounds known as c20-gibberellin 20-carboxylic acids. These are c20-gibberellins with a carboxyl group at the 6-position. Based on a literature review a small amount of articles have been published on Gibberellin A43. |
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Structure | [H][C@@]12CC[C@@H]3C[C@]1(CC3=C)[C@@H](C(O)=O)[C@@]1([H])[C@]2(C[C@H](O)[C@H](O)[C@@]1(C)C(O)=O)C(O)=O InChI=1S/C20H26O8/c1-8-5-19-6-9(8)3-4-11(19)20(17(27)28)7-10(21)14(22)18(2,16(25)26)13(20)12(19)15(23)24/h9-14,21-22H,1,3-7H2,2H3,(H,23,24)(H,25,26)(H,27,28)/t9-,10+,11-,12-,13-,14+,18+,19+,20-/m1/s1 |
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Synonyms | Value | Source |
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GA43 | HMDB | Gibberellin A43 | HMDB |
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Chemical Formula | C20H26O8 |
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Average Molecular Weight | 394.42 |
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Monoisotopic Molecular Weight | 394.162767797 |
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IUPAC Name | (1R,2S,3S,4S,5R,6S,8R,9R,12R)-5,6-dihydroxy-4-methyl-13-methylidenetetracyclo[10.2.1.0^{1,9}.0^{3,8}]pentadecane-2,4,8-tricarboxylic acid |
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Traditional Name | (1R,2S,3S,4S,5R,6S,8R,9R,12R)-5,6-dihydroxy-4-methyl-13-methylidenetetracyclo[10.2.1.0^{1,9}.0^{3,8}]pentadecane-2,4,8-tricarboxylic acid |
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CAS Registry Number | 54605-43-5 |
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SMILES | [H][C@@]12CC[C@@H]3C[C@]1(CC3=C)[C@@H](C(O)=O)[C@@]1([H])[C@]2(C[C@H](O)[C@H](O)[C@@]1(C)C(O)=O)C(O)=O |
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InChI Identifier | InChI=1S/C20H26O8/c1-8-5-19-6-9(8)3-4-11(19)20(17(27)28)7-10(21)14(22)18(2,16(25)26)13(20)12(19)15(23)24/h9-14,21-22H,1,3-7H2,2H3,(H,23,24)(H,25,26)(H,27,28)/t9-,10+,11-,12-,13-,14+,18+,19+,20-/m1/s1 |
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InChI Key | FQTLNSKVFLETSS-QBCIWLIXSA-N |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as c20-gibberellin 20-carboxylic acids. These are c20-gibberellins with a carboxyl group at the 6-position. |
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Kingdom | Organic compounds |
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Super Class | Lipids and lipid-like molecules |
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Class | Prenol lipids |
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Sub Class | Diterpenoids |
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Direct Parent | C20-gibberellin 20-carboxylic acids |
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Alternative Parents | |
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Substituents | - Gibberellane-6-carboxylic acid
- Gibberellane-20-carboxylic acid
- Tricarboxylic acid or derivatives
- Beta-hydroxy acid
- Hydroxy acid
- Cyclic alcohol
- Secondary alcohol
- 1,2-diol
- Carboxylic acid
- Carboxylic acid derivative
- Organic oxide
- Organooxygen compound
- Carbonyl group
- Organic oxygen compound
- Alcohol
- Hydrocarbon derivative
- Aliphatic homopolycyclic compound
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Molecular Framework | Aliphatic homopolycyclic compounds |
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External Descriptors | Not Available |
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Ontology |
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Physiological effect | Not Available |
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Disposition | |
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Process | |
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Role | |
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Physical Properties |
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State | Solid |
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Experimental Molecular Properties | Property | Value | Reference |
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Melting Point | Not Available | Not Available | Boiling Point | Not Available | Not Available | Water Solubility | Not Available | Not Available | LogP | Not Available | Not Available |
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Experimental Chromatographic Properties | Not Available |
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Predicted Molecular Properties | | Show more...
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Predicted Chromatographic Properties | Predicted Collision Cross SectionsPredictor | Adduct Type | CCS Value (Å2) | Reference |
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DeepCCS | [M-2H]- | 217.308 | 30932474 | DeepCCS | [M+Na]+ | 191.426 | 30932474 |
Predicted Kovats Retention IndicesUnderivatizedDerivatizedDerivative Name / Structure | SMILES | Kovats RI Value | Column Type | Reference |
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Gibberellin A43,1TMS,isomer #1 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O)[C@H](O)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 2979.1 | Semi standard non polar | 33892256 | Gibberellin A43,1TMS,isomer #2 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C)[C@H](O)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O | 3013.1 | Semi standard non polar | 33892256 | Gibberellin A43,1TMS,isomer #3 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O | 3022.4 | Semi standard non polar | 33892256 | Gibberellin A43,1TMS,isomer #4 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O | 3007.6 | Semi standard non polar | 33892256 | Gibberellin A43,1TMS,isomer #5 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O)[C@H](O)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O | 3003.7 | Semi standard non polar | 33892256 | Gibberellin A43,2TMS,isomer #1 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O)[C@H](O)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 2958.7 | Semi standard non polar | 33892256 | Gibberellin A43,2TMS,isomer #10 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O | 2978.8 | Semi standard non polar | 33892256 | Gibberellin A43,2TMS,isomer #2 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C)[C@H](O)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 2946.7 | Semi standard non polar | 33892256 | Gibberellin A43,2TMS,isomer #3 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 2955.3 | Semi standard non polar | 33892256 | Gibberellin A43,2TMS,isomer #4 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 2963.2 | Semi standard non polar | 33892256 | Gibberellin A43,2TMS,isomer #5 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@H](O)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O | 2966.9 | Semi standard non polar | 33892256 | Gibberellin A43,2TMS,isomer #6 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O | 2961.3 | Semi standard non polar | 33892256 | Gibberellin A43,2TMS,isomer #7 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O | 2967.8 | Semi standard non polar | 33892256 | Gibberellin A43,2TMS,isomer #8 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O | 2980.1 | Semi standard non polar | 33892256 | Gibberellin A43,2TMS,isomer #9 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O | 2985.0 | Semi standard non polar | 33892256 | Gibberellin A43,3TMS,isomer #1 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@H](O)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 2952.5 | Semi standard non polar | 33892256 | Gibberellin A43,3TMS,isomer #10 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O | 2981.8 | Semi standard non polar | 33892256 | Gibberellin A43,3TMS,isomer #2 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 2954.8 | Semi standard non polar | 33892256 | Gibberellin A43,3TMS,isomer #3 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 2952.0 | Semi standard non polar | 33892256 | Gibberellin A43,3TMS,isomer #4 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 2943.4 | Semi standard non polar | 33892256 | Gibberellin A43,3TMS,isomer #5 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 2960.5 | Semi standard non polar | 33892256 | Gibberellin A43,3TMS,isomer #6 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 2968.8 | Semi standard non polar | 33892256 | Gibberellin A43,3TMS,isomer #7 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O | 2959.2 | Semi standard non polar | 33892256 | Gibberellin A43,3TMS,isomer #8 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O | 2972.7 | Semi standard non polar | 33892256 | Gibberellin A43,3TMS,isomer #9 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O | 2958.9 | Semi standard non polar | 33892256 | Gibberellin A43,4TMS,isomer #1 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 2964.1 | Semi standard non polar | 33892256 | Gibberellin A43,4TMS,isomer #2 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 2979.5 | Semi standard non polar | 33892256 | Gibberellin A43,4TMS,isomer #3 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 3010.7 | Semi standard non polar | 33892256 | Gibberellin A43,4TMS,isomer #4 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 2978.2 | Semi standard non polar | 33892256 | Gibberellin A43,4TMS,isomer #5 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O | 2978.4 | Semi standard non polar | 33892256 | Gibberellin A43,5TMS,isomer #1 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C | 3040.8 | Semi standard non polar | 33892256 | Gibberellin A43,1TBDMS,isomer #1 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O)[C@H](O)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3220.7 | Semi standard non polar | 33892256 | Gibberellin A43,1TBDMS,isomer #2 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O | 3231.6 | Semi standard non polar | 33892256 | Gibberellin A43,1TBDMS,isomer #3 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O | 3227.7 | Semi standard non polar | 33892256 | Gibberellin A43,1TBDMS,isomer #4 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O | 3253.7 | Semi standard non polar | 33892256 | Gibberellin A43,1TBDMS,isomer #5 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@H](O)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O | 3248.9 | Semi standard non polar | 33892256 | Gibberellin A43,2TBDMS,isomer #1 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@H](O)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3426.1 | Semi standard non polar | 33892256 | Gibberellin A43,2TBDMS,isomer #10 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O | 3451.2 | Semi standard non polar | 33892256 | Gibberellin A43,2TBDMS,isomer #2 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3412.2 | Semi standard non polar | 33892256 | Gibberellin A43,2TBDMS,isomer #3 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3405.1 | Semi standard non polar | 33892256 | Gibberellin A43,2TBDMS,isomer #4 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3430.4 | Semi standard non polar | 33892256 | Gibberellin A43,2TBDMS,isomer #5 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O | 3434.5 | Semi standard non polar | 33892256 | Gibberellin A43,2TBDMS,isomer #6 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O | 3400.9 | Semi standard non polar | 33892256 | Gibberellin A43,2TBDMS,isomer #7 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O | 3436.9 | Semi standard non polar | 33892256 | Gibberellin A43,2TBDMS,isomer #8 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O | 3424.5 | Semi standard non polar | 33892256 | Gibberellin A43,2TBDMS,isomer #9 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O | 3437.1 | Semi standard non polar | 33892256 | Gibberellin A43,3TBDMS,isomer #1 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3606.9 | Semi standard non polar | 33892256 | Gibberellin A43,3TBDMS,isomer #10 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O | 3628.1 | Semi standard non polar | 33892256 | Gibberellin A43,3TBDMS,isomer #2 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3601.8 | Semi standard non polar | 33892256 | Gibberellin A43,3TBDMS,isomer #3 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3619.2 | Semi standard non polar | 33892256 | Gibberellin A43,3TBDMS,isomer #4 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3595.7 | Semi standard non polar | 33892256 | Gibberellin A43,3TBDMS,isomer #5 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3619.0 | Semi standard non polar | 33892256 | Gibberellin A43,3TBDMS,isomer #6 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3616.1 | Semi standard non polar | 33892256 | Gibberellin A43,3TBDMS,isomer #7 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O | 3599.5 | Semi standard non polar | 33892256 | Gibberellin A43,3TBDMS,isomer #8 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O | 3630.5 | Semi standard non polar | 33892256 | Gibberellin A43,3TBDMS,isomer #9 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O | 3606.6 | Semi standard non polar | 33892256 | Gibberellin A43,4TBDMS,isomer #1 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3769.1 | Semi standard non polar | 33892256 | Gibberellin A43,4TBDMS,isomer #2 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3801.5 | Semi standard non polar | 33892256 | Gibberellin A43,4TBDMS,isomer #3 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3819.4 | Semi standard non polar | 33892256 | Gibberellin A43,4TBDMS,isomer #4 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C | 3793.5 | Semi standard non polar | 33892256 | Gibberellin A43,4TBDMS,isomer #5 | C=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C(=O)O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@](C)(C(=O)O[Si](C)(C)C(C)(C)C)[C@H]1[C@@H]3C(=O)O | 3782.9 | Semi standard non polar | 33892256 |
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Spectra |
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| GC-MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
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Predicted GC-MS | Predicted GC-MS Spectrum - Gibberellin A43 GC-MS (Non-derivatized) - 70eV, Positive | Not Available | 2021-10-12 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Gibberellin A43 GC-MS (Non-derivatized) - 70eV, Positive | Not Available | 2021-10-12 | Wishart Lab | View Spectrum |
MS/MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
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Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Gibberellin A43 10V, Negative-QTOF | splash10-0f6y-0009000000-a8083a5ea03e3e387c7b | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Gibberellin A43 20V, Negative-QTOF | splash10-0zfr-0009000000-ec96b841820fa214bd10 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Gibberellin A43 40V, Negative-QTOF | splash10-0a4l-9433000000-d9d91849a19b2b0a20a3 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Gibberellin A43 10V, Positive-QTOF | splash10-0002-0009000000-9e6a894d4134421764eb | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Gibberellin A43 20V, Positive-QTOF | splash10-0002-0009000000-8df66fc6e76d3de33ab8 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Gibberellin A43 40V, Positive-QTOF | splash10-0092-0209000000-f61d65d410bb4af0d7dc | 2021-09-22 | Wishart Lab | View Spectrum |
NMR SpectraSpectrum Type | Description | Deposition Date | Source | View |
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Predicted 1D NMR | 1H NMR Spectrum (1D, 100 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 100 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 1000 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 1000 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 200 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 200 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 300 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 300 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 400 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 400 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 500 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 500 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 600 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 600 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 700 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 700 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 800 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 800 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 900 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 900 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum |
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Biological Properties |
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Cellular Locations | - Cytoplasm
- Extracellular
- Membrane
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Biospecimen Locations | Not Available |
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Tissue Locations | Not Available |
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Pathways | |
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Normal Concentrations |
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| Not Available |
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Abnormal Concentrations |
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| Not Available |
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Associated Disorders and Diseases |
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Disease References | None |
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Associated OMIM IDs | None |
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External Links |
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DrugBank ID | Not Available |
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Phenol Explorer Compound ID | Not Available |
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FooDB ID | FDB013663 |
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KNApSAcK ID | C00000043 |
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Chemspider ID | 103885428 |
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KEGG Compound ID | Not Available |
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BioCyc ID | CPD-6222 |
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BiGG ID | Not Available |
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Wikipedia Link | Not Available |
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METLIN ID | Not Available |
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PubChem Compound | 25243967 |
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PDB ID | Not Available |
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ChEBI ID | Not Available |
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Food Biomarker Ontology | Not Available |
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VMH ID | Not Available |
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MarkerDB ID | Not Available |
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Good Scents ID | Not Available |
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References |
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Synthesis Reference | Not Available |
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Material Safety Data Sheet (MSDS) | Not Available |
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General References | - Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
- Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
- Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
- Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
- (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
- Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.
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