(Q7280510)

inferred from isomeric SMILES

stereoisomer of

(-)-N-methylcytisine

2 references

(4S,6S,8R,9Z,11E)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.06,8]nonadeca-1(15),9,11,16,18-pentaene-2,13-dione

inferred from InChI

2 references

2 references

(4S,6S,8S,9Z,11E)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.06,8]nonadeca-1(15),9,11,16,18-pentaene-2,13-dione

1 reference

1 reference

(4R,6S,8R)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.06,8]nonadeca-1(15),9,11,16,18-pentaene-2,13-dione

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₁₈H₁₇ClO₆

1 reference

PubChem

canonical SMILES

O=C1\C=C\C=C/C3OC3CC(C)OC(=O)c2c(O)cc(O)c(Cl)c2C1

1 reference

heat shock protein Hsp90 family

isomeric SMILES

C[C@@H]1C[C@@H]2[C@H](O2)/C=CC=CC(=O)Cc3c(c(cc(c3Cl)O)O)C(=O)O1

0 references

inhibitor of

protein tyrosine kinase

1 reference

25 February 2021

1 reference

25 February 2021

Didymosporium radicicola

1 reference

"Castaneiolide, abscisic acid and monorden, phytotoxic compounds isolated from fungi (Macrophoma castaneicola and Didymosporium radicicola) cause \"black root rot disease\" in chestnut trees."

Humicola fuscoatra

2 references

Antifungal Metabolites (Monorden, Monocillin IV, and Cerebrosides) from Humicola fuscoatra Traaen NRRL 22980, a Mycoparasite of Aspergillus flavus Sclerotia

Study of marine natural products including resorcyclic acid lactones from Humicola fuscoatra that reactivate latent HIV-1 expression in an in vitro model of central memory CD4+ T cells

Monocillium nordinii

1 reference

Minor metabolites of Monocillium nordinii

Neocosmospora boninensis

1 reference

Production of cyclosporin by fungi belonging to the genus Neocosmospora.

Neocosmospora tenuicristata

3 references

Monorden from a novel source, Neocosmospora tenuicristata: Stereochemistry and plant growth regulatory properties.

Monorden from a novel source, Neocosmospora tenuicristata: Stereochemistry and plant growth regulatory properties.

Induction of differentiation of HL-60 cells by the anti-fungal antibiotic, radicicol.

Fusarium neocosmosporiellum

1 reference

Production of cyclosporin by fungi belonging to the genus Neocosmospora.

Fusarium tenuicristatum

2 references

Monorden from a novel source, Neocosmospora tenuicristata: Stereochemistry and plant growth regulatory properties.

Induction of differentiation of HL-60 cells by the anti-fungal antibiotic, radicicol.

Trichobotrys effusus

1 reference

Aliphatic phenolic ethers from Trichobotrys effusa

Trichobotrys effusa

1 reference

Aliphatic phenolic ethers from Trichobotrys effusa

Niesslia nordinii

1 reference

Minor metabolites of Monocillium nordinii

Metacordyceps chlamydosporia

1 reference

Pochonins A-F, new antiviral and antiparasitic resorcylic acid lactones from Pochonia chlamydosporia var. catenulata

Floropilus chiversii

1 reference

Uncovering biosynthetic potential of plant-associated fungi: effect of culture conditions on metabolite production by Paraphaeosphaeria quadriseptata and Chaetomium chiversii

Neophaeosphaeria quadriseptata

1 reference

Uncovering biosynthetic potential of plant-associated fungi: effect of culture conditions on metabolite production by Paraphaeosphaeria quadriseptata and Chaetomium chiversii

subject has role

enzyme inhibitor

1 reference

15 March 2018

1 reference

15 March 2018

1 reference

InChI=1S/C18H17ClO6/c1-9-6-15-14(25-15)5-3-2-4-10(20)7-11-16(18(23)24-9)12(21)8-13(22)17(11)19/h2-5,8-9,14-15,21-22H,6-7H2,1H3/b4-2+,5-3-/t9-,14-,15-/m1/s1

15 March 2018

Proposed Radicicol Biosynthetic Pathway.png
1,779 × 1,583; 53 KB

0 references

Identifiers

InChI

1 reference

PubChem

2 references

PubChem

ChEBI release 2020-09-01

CAS Registry Number

12772-57-5

2 references

https://commonchemistry.cas.org/detail?cas_rn=12772-57-5

8 April 2021

ChemSpider ID

16735913

1 reference

PubChem CID

6323491

1 reference

ChEBI ID

556075

mapping relation type

exact match

3 references

ChEBI release 2019-10-02

International Chemical Identifier

InChI

InChI=1S/C18H17ClO6/c1-9-6-15-14(25-15)5-3-2-4-10(20)7-11-16(18(23)24-9)12(21)8-13(22)17(11)19/h2-5,8-9,14-15,21-22H,6-7H2,1H3/b4-2+,5-3-/t9-,14-,15-/m1/s1

ChEMBL ID

CHEMBL453386

1 reference

2 references

DSSTOX compound identifier

1 reference

0 references

0 references

0 references

642-889-3

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.170.695

retrieved

27 December 2018

title

(4R,6R,8R,9Z,11E)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(15),9,11,16,18-pentaene-2,13-dione (English)

quotation

CAS no.: 12772-57-5 (English)

ECHA Substance Infocard ID

100.170.695

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.170.695

retrieved

27 December 2018

title

(4R,6R,8R,9Z,11E)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(15),9,11,16,18-pentaene-2,13-dione (English)

quotation

CAS no.: 12772-57-5 (English)

MeSH descriptor ID

C035359

1 reference

14 March 2018

0 references

1 reference

UNII

I60EH8GECX

1 reference