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(Q104403330)
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Emindole Sb
chemical compound
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Statements
instance of
type of chemical entity
0 references
subclass of
1,16,20-Trimethyl-16-(4-methylpent-3-enyl)-3-azapentacyclo[10.8.0.02,10.04,9.015,20]icosa-2(10),4,6,8-tetraen-17-ol
1 reference
based on heuristic
inferred from SMILES
mass
405.303164868
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₂₈H₃₉NO
0 references
canonical SMILES
OC1CCC2(C)C(CCC3CC=4C=5C=CC=CC5NC4C32C)C1(C)CCC=C(C)C
0 references
isomeric SMILES
CC(C)=CCC[C@]1(C)[C@@H](O)CC[C@@]2(C)[C@H]1CC[C@H]1Cc3c([nH]c4ccccc34)[C@@]12C
0 references
found in taxon
Albophoma yamanashiensis
1 reference
stated in
Terpendoles, novel ACAT inhibitors produced by Albophoma yamanashiensis. I. Production, isolation and biological properties.
Aspergillus flavus
3 references
stated in
Reconstitution of biosynthetic machinery for indole-diterpene paxilline in Aspergillus oryzae
stated in
Indoloditerpenes from an algicolous isolate of Aspergillus oryzae.
stated in
Indoloditerpenes from an algicolous isolate of Aspergillus oryzae.
Aspergillus striatus
1 reference
stated in
Isolation and structures of indoloditerpenes, possible biosynthetic intermediates to the tremorgenic mycotoxin, paxilline, from Emericella striata
Penicillium thiersii
1 reference
stated in
Thiersinines A and B: novel antiinsectan indole diterpenoids from a new fungicolous Penicillium species (NRRL 28147).
Penicillium camemberti
1 reference
stated in
Indole-diterpenoids with anti-H1N1 activity from the aciduric fungus Penicillium camemberti OUCMDZ-1492.
Aspergillus cejpii
1 reference
stated in
Indoloditerpenes from a marine-derived fungal strain of Dichotomomyces cejpii with antagonistic activity at GPR18 and cannabinoid receptors.
Dichotomomyces cejpii
1 reference
stated in
Indoloditerpenes from a marine-derived fungal strain of Dichotomomyces cejpii with antagonistic activity at GPR18 and cannabinoid receptors.
Penicillium
1 reference
stated in
Indole Diterpenoids from an Endophytic Penicillium sp
Fusarium
1 reference
stated in
l-Tryptophan Induces a Marine-Derived Fusarium sp. to Produce Indole Alkaloids with Activity against the Zika Virus
Identifiers
InChI
InChI=1S/C28H39NO/c1-18(2)9-8-15-26(3)23-13-12-19-17-21-20-10-6-7-11-22(20)29-25(21)28(19,5)27(23,4)16-14-24(26)30/h6-7,9-11,19,23-24,29-30H,8,12-17H2,1-5H3/t19-,23-,24-,26-,27-,28+/m0/s1
0 references
InChIKey
XOLHQUYGSUGTQA-DFGZTGKASA-N
0 references
PubChem CID
9887568
2 references
stated in
PubChem
retrieved
17 September 2022
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
XOLHQUYGSUGTQA-DFGZTGKASA-N
ChEBI ID
192683
mapping relation type
exact match
1 reference
matched by identifier from
International Chemical Identifier
InChI
InChI=1S/C28H39NO/c1-18(2)9-8-15-26(3)23-13-12-19-17-21-20-10-6-7-11-22(20)29-25(21)28(19,5)27(23,4)16-14-24(26)30/h6-7,9-11,19,23-24,29-30H,8,12-17H2,1-5H3/t19-,23-,24-,26-,27-,28+/m0/s1
UniChem compound ID
727883
1 reference
stated in
UniChem
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