Microcyclamide GL614A
bioactive natural product
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Microcyclamide GL614A
Summary
Microcyclamide GL614A is a group of stereoisomers[1].
Key Facts
- Microcyclamide GL614A's instance of is recorded as group of stereoisomers[2].
- Microcyclamide GL614A's canonical SMILES is recorded as CCC(C)C1NC(=O)c2nc(oc2C)C(C)NC(=O)c2csc(n2)C(CC2C(=O)NC(=O)N2C)NC(=O)c2csc1n2[3].
- Microcyclamide GL614A's InChI is recorded as InChI=1S/C26H30N8O6S2/c1-6-10(2)17-25-30-15(9-42-25)20(36)28-13(7-16-21(37)33-26(39)34(16)5)24-29-14(8-41-24)19(35)27-11(3)23-32-18(12(4)40-23)22(38)31-17/h8-11,13,16-17H,6-7H2,1-5H3,(H,27,35)(H,28,36)(H,31,38)(H,33,37,39)/t10-,11-,13-,16?,17-/m0/s1[4].
- Microcyclamide GL614A's InChIKey is recorded as YMVUMOCTCMIYEH-YQNZXUTESA-N[5].
- Microcyclamide GL614A's chemical formula is recorded as C₂₆H₃₀N₈O₆S₂[6].
- Microcyclamide GL614A's subclass of is recorded as biogenic cyclopeptide[7].
- Microcyclamide GL614A's subclass of is recorded as thiazole alkaloid[8].
- Microcyclamide GL614A's subclass of is recorded as oxazole alkaloid[9].
- Microcyclamide GL614A's PubChem CID is recorded as 46197154[10].
- Microcyclamide GL614A's ChEBI ID is recorded as 200716[11].
- Microcyclamide GL614A's found in taxon is recorded as Microcystis[12].
- Microcyclamide GL614A's isomeric SMILES is recorded as CCC@H[C@@H]1NC(=O)c2nc(oc2C)C@HNC(=O)c2csc(n2)C@HNC(=O)c2csc1n2C@H[C@@H]1NC(=O)c2nc(oc2C)C@HNC(=O)c2csc(n2)C@HNC(=O)c2csc1n2">[13].
- Microcyclamide GL614A's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+614.17297268'}[14].
- Microcyclamide GL614A's SureChEMBL ID is recorded as 29884686[15].
- Microcyclamide GL614A's DSSTox substance ID is recorded as DTXSID001333894[16].
- Microcyclamide GL614A's Natural Product Atlas ID is recorded as NPA003675[17].
- Microcyclamide GL614A's UniChem compound ID is recorded as 33233905[18].