CID 45934402

For Research Use Only.
Category
Sesquiterpene
Cat.No.
NP5587
CAS
163391-76-2
Product Name
CID 45934402
Structure

Product Details

Description
An unusual spirodihydrobenzofuranlactam mycotoxin isolated from Stachybotrys sp. It shows immunosuppressant and weak HIV protease activity and shows diverse activity including antiviral, endothelin and pancreatic cholesterase inhibition.
Synonyms
Stachybotrylactam;163391-76-2;3,4'-dihydroxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-7,8-dihydro-3H-furo[2,3-e]isoindole]-6'-one;Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-6(3H)-one, 3',4',4'a,5',6',7,7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-, (1'R,2'R,4'aS,6'R,8'aS)-;CID 45934402;Compound NP-020819;DTXSID70672955;CHEBI:201797;AKOS040737949;J-010041;(3R,4aS,7R,8R,8aS)-3,4'-dihydroxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-7,8-dihydro-3H-uro[2,3-e]isoindole]-6'-one;4,6'-DIHYDROXY-2',5',5',8'A-TETRAMETHYL-3',4',4'A,6',7,7',8,8'-OCTAHYDRO-2'H,3H-SPIRO[FURO[2,3-E]ISOINDOLE-2,1'-NAPHTHALEN]-6-ONE;
IUPAC Name
3,4'-dihydroxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-7,8-dihydro-3H-furo[2,3-e]isoindole]-6'-one
Molecular Weight
385.50
Molecular Formula
C23H31NO4
Canonical SMILES
O=C1NCC2=C1C=C(C3=C2O[C@@]4(C3)[C@](C)([C@]5(CC[C@H]4C)[H])CC[C@H](C5(C)C)O)O
InChI
InChI=1S/C23H31NO4/c1-12-5-6-17-21(2,3)18(26)7-8-22(17,4)23(12)10-14-16(25)9-13-15(19(14)28-23)11-24-20(13)27/h9,12,17-18,25-26H,5-8,10-11H2,1-4H3,(H,24,27)
InChIKey
ZSVLMDBFFSSVAK-UHFFFAOYSA-N
Boiling Point
630.0±55.0°C (Predicted)
Melting Point
210°C (dec.)
Purity
>95% by HPLC
Density
1.28±0.1 g/cm3 (Predicted)
Solubility
Soluble in Ethanol, Methanol, DMF, DMSO; Poorly soluble in Water
Appearance
White to Off-white Solid
Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Form
Neat
pKa
9.39±0.70(Predicted)
Uses
Stachybotrylactam is an unusual, spirodihydrobenzofuranlactam mycotoxin isolated from a Stachybotrys sp., showing immunosuppressant and weak HIV protease activity. Members of this structural class show diverse activity including antiviral, endothelin and pancreatic cholesterase inhibition.
WGK Germany
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