Jasmonic Acid

Jasmonic Acid

SCHEMBL1365045

CCC=CCC1C(=O)CCC1CC(=O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AKR1C4 P17516 1/20 1.00
AKR1C3 P42330 1/20 1.00
AKR1C2 P52895 1/20 1.00
HTT P42858 1/20 0.44
PTGER2 P43116 11/20 0.39
PTGER4 P35408 5/20 0.37
PTGER3 P43115 4/20 0.37
TBXA2R P21731 3/20 0.32
PTGIR P43119 2/20 0.32
NR1I2 O75469 1/20 0.32
ESR1 P03372 1/20 0.32
PGR P06401 1/20 0.32
HPGD P15428 1/20 0.32
TSHR P16473 1/20 0.32
MAPK1 P28482 1/20 0.32
PTGER1 P34995 1/20 0.32
OPRK1 P41145 1/20 0.32
PTGFR P43088 1/20 0.32
PDE4D Q08499 1/20 0.32
FFAR1 O14842 1/20 0.31

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Jasmonic Acid SCHEMBL114054 1.00 AKR1C4 (1.00) AKR1C4AKR1C3AKR1C2HTTPTGER2
Jasmonic Acid SCHEMBL7113180 1.00 AKR1C4 (1.00) AKR1C4AKR1C3AKR1C2HTTPTGER2
Jasmonic Acid SCHEMBL125395 1.00 AKR1C4 (1.00) AKR1C4AKR1C3AKR1C2HTTPTGER2
Jasmonic Acid SCHEMBL12216372 1.00 AKR1C4 (1.00) AKR1C4AKR1C3AKR1C2HTTPTGER2
Jasmonic Acid SCHEMBL7113179 1.00 AKR1C4 (1.00) AKR1C4AKR1C3AKR1C2HTTPTGER2
Jasmonic Acid SCHEMBL3074832 1.00 AKR1C4 (1.00) AKR1C4AKR1C3AKR1C2HTTPTGER2
Jasmonic Acid SCHEMBL4360733 1.00 AKR1C4 (1.00) AKR1C4AKR1C3AKR1C2HTTPTGER2
Jasmonic Acid SCHEMBL5598513 1.00 AKR1C4 (1.00) AKR1C4AKR1C3AKR1C2HTTPTGER2
Jasmonic Acid SCHEMBL1365044 1.00 AKR1C4 (1.00) AKR1C4AKR1C3AKR1C2HTTPTGER2
Jasmonic Acid SCHEMBL6734659 1.00 AKR1C4 (1.00) AKR1C4AKR1C3AKR1C2HTTPTGER2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 102 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220142158-A1 ARTHROPOD CONTROL COMPOSITIONS FIRMENICH SA (CH) 2022-05-12 US claimed
EP-3930460-A1 ARTHROPOD CONTROL COMPOSITIONS Firmenich SA (CH) 2022-01-05 EP claimed
CN-112638861-A Process for preparing cis-alpha, beta-substituted cyclopentanones 弗门尼舍有限公司 2021-04-09 CN claimed
WO-2020239954-A1 ARTHROPOD CONTROL COMPOSITIONS FIRMENICH SA (CH) 2020-12-03 WO claimed
CN-106518471-A Nutrient solution for grape planting 华蓥市德嘉葡萄专业合作社 2017-03-22 CN claimed
US-20160101083-A1 ANTI-PARASITIC METHODS AND COMPOSITIONS UTILIZING DIINDOLYLMETHANE-RELATED INDOLES BIORESPONSE, L.L.C. (US) 2016-04-14 US claimed
US-20140037577-A1 ANTI-PARASITIC METHODS AND COMPOSITIONS UTILIZING DIINDOLYLMETHANE-RELATED INDOLES BIORESPONSE, L.L.C. 2014-02-06 US claimed
US-8586621-B2 Anti-parasitic methods and compositions utilizing diindolylmethane-related indoles BIORESPONSE, L.L.C. 2013-11-19 US claimed
WO-2012034825-A3 FLUORINE GAS PLANT SOLVAY SA (BE) 2012-05-10 WO claimed
EP-1333022-B1 Compounds containing derivatives of cyclopentane and their use to stimulate skin peeling OREAL (FR) 2011-12-07 EP claimed
US-20100055201-A1 ANTI-PARASITIC METHODS AND COMPOSITIONS UTILIZING DIINDOLYLMETHANE-RELATED INDOLES BIORESPONSE, L.L.C. 2010-03-04 US claimed
WO-2008057253-A2 ANTI-PARASITIC METHODS AND COMPOSITIONS UTILIZING DIINDOLYLMETHANE-RELATED INDOLES BIORESPONSE, L.L.C. (US) 2008-05-15 WO claimed
US-20030224024-A1 Compositions comprising cyclopentane derivatives and their use L'OREAL S.A. (FR) 2003-12-04 US claimed
EP-1333022-A2 Compounds containing derivatives of cyclopentane and their use to stimulate skin peeling L'OREAL (FR) 2003-08-06 EP claimed
EP-0743985-B1 METHOD FOR PREPARING CYCLIC KETONES FIRMENICH & CIE (CH) 2000-10-11 EP claimed
US-5667995-A MICROORGANISM CULTURE, BETA-OXIDATION, BIOSYNTHESIS FIRMENICH SA (CH) 1997-09-16 US claimed
US-20250312349-A1 COMPOSITION AND METHODS OF TREATING INTRACELLULAR PATHOGEN INFECTION UNIV HOSPITALS CLEVELAND MEDICAL CENTER (US) 2025-10-09 US disclosed
US-20250073255-A1 USE OF FA-TYPE LIPID COMPOUNDS IN PREPARATION OF NUCLEIC ACID DELIVERY REAGENT AND RELATED PRODUCT BEIJING BAISHIHEKANG PHARMACEUTICAL TECHNOLOGY (BSJPHARMA) CO., LTD (CN) 2025-03-06 US disclosed
WO-1996018742-A1 METHOD FOR PREPARING CYCLIC KETONES FIRMENICH S.A. (CH) 1996-06-20 WO disclosed
US-3941828-A Process for the preparation of cyclic ketones FIRMENICH SA (CH) 1976-03-02 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20160101083-A1 ANTI-PARASITIC METHODS AND COMPOSITIONS UTILIZING DIINDOLYLMETHANE-RELATED INDOLES CASP3, IDO1, INMT AKR1C4 4234/4885AKR1C3 3259/4885AKR1C2 3590/4885
US-20250073255-A1 USE OF FA-TYPE LIPID COMPOUNDS IN PREPARATION OF NUCLEIC ACID DELIVERY REAGENT AND RELATED PRODUCT FABP2, FABP1, FASN AKR1C4 1801/4885AKR1C3 1860/4885AKR1C2 1318/4885
US-20100055201-A1 ANTI-PARASITIC METHODS AND COMPOSITIONS UTILIZING DIINDOLYLMETHANE-RELATED INDOLES CASP3, IDO1, INMT AKR1C4 4234/4885AKR1C3 3259/4885AKR1C2 3590/4885
US-20140037577-A1 ANTI-PARASITIC METHODS AND COMPOSITIONS UTILIZING DIINDOLYLMETHANE-RELATED INDOLES CASP3, IDO1, INMT AKR1C4 4234/4885AKR1C3 3259/4885AKR1C2 3590/4885
US-20030224024-A1 Compositions comprising cyclopentane derivatives and their use CBR1, CBR3, DECR1 AKR1C4 34/4885AKR1C3 23/4885AKR1C2 71/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.