(Q110183496)

English

CID 71307573

chemical compound

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Statements

type of chemical entity

0 references

sphenolobane diterpenoid

1 reference

based on heuristic

inferred from SMILES

432.178417856 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

(2E,4E)-5-[(1R,7S,8S,9R)-7-(acetyloxy)-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid

1 reference

based on heuristic

inferred from InChI

(2E,4E)-5-[(1R,7S,8S,9S)-7-acetyloxy-4-methoxycarbonyl-9-methyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₃H₂₈O₈

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canonical SMILES

O=C(O)C(=CC=CC1(OC(=O)C23CC=C(C(=O)OC)CCC3(OC(=O)C)C1CC2)C)C

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isomeric SMILES

COC(=O)C1=CC[C@@]23CC[C@H]([C@@]2(OC(C)=O)CC1)[C@@](C)(/C=C/C=C(\C)C(=O)O)OC3=O

0 references

Pseudolarix amabilis

8 references

Cytotoxic diterpenoids from the bark of Pseudolarix kaempferi and their structure-activity relationships.

Recent advances in chemical studies on the active principles from plants forfertility regulation

Five new diterpenoids from Pseudolarix kaempferi

Antifungal Diterpenoids of Pseudolarix kaempferi, and Their Structure—Activity Relationship Study.

Antifungal evaluation of pseudolaric acid B, a major constituent of Pseudolarix kaempferi

Pseudolaric acids from Pseudolarix kaempferi

Evaluation of the interaction of bioactive compounds in Cortex Pseudolarix and Radix Stephaniae by the microdialysis probe coupled with high performance liquid chromatography-mass spectrometry

Interaction of pseudolaric acid B with the colchicine site of tubulin

Larix kaempferi

8 references

Cytotoxic diterpenoids from the bark of Pseudolarix kaempferi and their structure-activity relationships.

Recent advances in chemical studies on the active principles from plants forfertility regulation

Five new diterpenoids from Pseudolarix kaempferi

Antifungal Diterpenoids of Pseudolarix kaempferi, and Their Structure—Activity Relationship Study.

Antifungal evaluation of pseudolaric acid B, a major constituent of Pseudolarix kaempferi

Pseudolaric acids from Pseudolarix kaempferi

Evaluation of the interaction of bioactive compounds in Cortex Pseudolarix and Radix Stephaniae by the microdialysis probe coupled with high performance liquid chromatography-mass spectrometry

Interaction of pseudolaric acid B with the colchicine site of tubulin

Identifiers

InChI=1S/C23H28O8/c1-14(18(25)26)6-5-10-21(3)17-9-12-22(20(28)31-21)11-7-16(19(27)29-4)8-13-23(17,22)30-15(2)24/h5-7,10,17H,8-9,11-13H2,1-4H3,(H,25,26)/b10-5+,14-6+/t17-,21+,22-,23-/m0/s1

0 references

VDGOFNMYZYBUDT-YCONPBHISA-N

0 references

2 references

17 September 2022

based on heuristic

inferred from InChIKey

matched by identifier from

VDGOFNMYZYBUDT-YCONPBHISA-N

mapping relation type

2 references

ChEBI release 2022-06-13

matched by identifier from

International Chemical Identifier

InChI=1S/C23H28O8/c1-14(18(25)26)6-5-10-21(3)17-9-12-22(20(28)31-21)11-7-16(19(27)29-4)8-13-23(17,22)30-15(2)24/h5-7,10,17H,8-9,11-13H2,1-4H3,(H,25,26)/b10-5+,14-6+/t17-,21+,22-,23-/m0/s1

UniChem compound ID

1 reference

Probes And Drugs ID

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