(3R,6R,9S,12S,15S,18S,24S,27S,30S,33S)-27-[(1R,2R,4E)-1-hydroxy-2-methylhex-4-en-1-yl]-24-[(1R)-1-hydroxyethyl]-15,30-diisopropyl-1,4,6,9,13,19,22,28-octamethyl-3,12,18,33-tetrakis(2-methylpropyl)-1,4,7,10,13,16,19,22,25,28,31-undecaazacyclotritriacontan-
AlkaPlorer ID: AK081143
Synonym: None
IUPAC Name: (3R,6R,9S,12S,15S,18S,24S,27S,30S,33S)-24-[(1R)-1-hydroxyethyl]-27-[(E,1R,2R)-1-hydroxy-2-methylhex-4-enyl]-1,4,6,9,13,19,22,28-octamethyl-3,12,18,33-tetrakis(2-methylpropyl)-15,30-di(propan-2-yl)-1,4,7,10,13,16,19,22,25,28,31-undecazacyclotritriacontane-2,5,8,11,14,17,20,23,26,29,32-undecone
Structure
SMILES: C/C=C/C[C@@H](C)[C@@H](O)[C@H]1C(O)=N[C@@H]([C@@H](C)O)C(=O)N(C)CC(=O)N(C)[C@@H](CC(C)C)C(O)=N[C@@H](C(C)C)C(=O)N(C)[C@@H](CC(C)C)C(O)=N[C@@H](C)C(O)=N[C@H](C)C(=O)N(C)[C@H](CC(C)C)C(=O)N(C)[C@@H](CC(C)C)C(O)=N[C@@H](C(C)C)C(=O)N1C
InChI: InChI=1S/C61H109N11O13/c1-24-25-26-38(14)51(75)50-56(80)66-49(41(17)73)59(83)67(18)31-46(74)68(19)42(27-32(2)3)54(78)64-47(36(10)11)60(84)70(21)43(28-33(4)5)53(77)62-39(15)52(76)63-40(16)57(81)71(22)45(30-35(8)9)58(82)69(20)44(29-34(6)7)55(79)65-48(37(12)13)61(85)72(50)23/h24-25,32-45,47-51,73,75H,26-31H2,1-23H3,(H,62,77)(H,63,76)(H,64,78)(H,65,79)(H,66,80)/b25-24+/t38-,39+,40-,41-,42+,43+,44+,45-,47+,48+,49+,50+,51-/m1/s1
InChIKey: VHAAQDUGYGVCKU-LPOYGZCQSA-N
Reference
Neue Cyclosporine aus <i>Tolypocladium inflatum</i>. Die Cyclosporine K–Z
PubChem CID: 163023076
LOTUS: LTS0096821
SuperNatural Ⅲ: SN0390109-02
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Tolypocladium inflatum | Tolypocladium | Ophiocordycipitaceae | Hypocreales | Sordariomycetes | Ascomycota | Fungi | Eukaryota |
Properties Information
Molecule Weight: 1204.606999999999
TPSA?: 325.27
MolLogP?: 6.099100000000021
Number of H-Donors: 7
Number of H-Acceptors: 13
RingCount: 1
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|
