Navigation

name Structure Reference Source Properties Activities Metabolism

(3aR,8aR)-7-[(3aR,8aR)-1-methyl-2H,3H,8H,8aH-pyrrolo[2,3-b]indol-3a-yl]-3a-[(3aS,8aS)-7-[(3aR,8aR)-7-[(3aS,8aS)-7-[(3aR,8aR)-1-methyl-2H,3H,8H,8aH-pyrrolo[2,3-b]indol-3a-yl]-1-methyl-2H,3H,8H,8aH-pyrrolo[2,3-b]indol-3a-yl]-1-methyl-2H,3H,8H,8aH-pyrrolo[2,

AlkaPlorer ID: AK139083

Synonym: None

IUPAC Name: (3aS,8bS)-5-[(3aR,8bR)-5-[(3aS,8bS)-5-[(3aR,8bR)-3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indol-8b-yl]-3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indol-8b-yl]-3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indol-8b-yl]-8b-[(3aR,8bR)-5-[(3aR,8bR)-3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indol-8b-yl]-3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indol-8b-yl]-3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indole

Structure

SMILES: CN1CC[C@]2(C3=CC=CC4=C3N[C@H]3N(C)CC[C@@]43C3=CC=CC4=C3N[C@@H]3N(C)CC[C@]43C3=CC=CC4=C3N[C@H]3N(C)CC[C@@]43[C@]34CCN(C)[C@H]3NC3=C([C@]56CCN(C)[C@H]5NC5=CC=CC=C56)C=CC=C34)C3=CC=CC=C3N[C@H]12

copy

InChI: InChI=1S/C66H74N12/c1-73-33-27-61(39-15-7-9-25-49(39)67-55(61)73)41-17-11-18-42-51(41)69-57-63(42,29-35-75(57)3)43-19-12-20-44-52(43)70-58-64(44,30-36-76(58)4)46-22-14-24-48-54(46)72-60-66(48,32-38-78(60)6)65-31-37-77(5)59(65)71-53-45(21-13-23-47(53)65)62-28-34-74(2)56(62)68-50-26-10-8-16-40(50)62/h7-26,55-60,67-72H,27-38H2,1-6H3/t55-,56-,57+,58-,59-,60+,61-,62-,63+,64-,65+,66-/m1/s1

copy

InChIKey: BXKLGDDYHDKOIO-IRUIJRKLSA-N

copy

Source

Species Genus Family Order Class Phylum Kingdom Domain
Psychotria milnei Psychotria Rubiaceae Gentianales Magnoliopsida Streptophyta Viridiplantae Eukaryota

Properties Information

Molecule Weight: 1035.4019999999994

TPSA？: 91.62

MolLogP？: 8.529400000000008

Number of H-Donors: 6

Number of H-Acceptors: 12

RingCount: 18

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi

Metabolism Information