Epoprostenol

Epoprostenol

SCHEMBL24033081

CCCCC[C@H](O)/C=C/[C@@H]1C2C/C(=C/CCCC(=O)O)O[C@H]2C[C@H]1O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PTGIR

The experimentally established mechanism targets of Epoprostenol. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTGIR known ✓ P43119 6/20 0.56
ALDH1A1 P00352 5/20 1.00
MEN1 O00255 2/20 0.71
KMT2A Q03164 2/20 0.71
PPARD Q03181 2/20 0.71
PPARA Q07869 2/20 0.71
PPARG P37231 1/20 0.71
PTGER4 P35408 4/20 0.56
TBXA2R P21731 3/20 0.56
PTGER1 P34995 2/20 0.56
PTGFR P43088 2/20 0.56
PTGER3 P43115 2/20 0.56
LMNA P02545 2/20 0.56
PTGDR Q13258 1/20 0.56
SLCO2A1 Q92959 1/20 0.56
PTGER2 P43116 3/20 0.56
TSHR P16473 3/20 0.56
HPGD P15428 2/20 0.56
MAPK1 P28482 2/20 0.56
NR1I2 O75469 1/20 0.56

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
Epoprostenol SCHEMBL551616 1.00 ALDH1A1 (1.00) ALDH1A1MEN1KMT2APPARDPPARA
Epoprostenol SCHEMBL16783375 1.00 ALDH1A1 (1.00) ALDH1A1MEN1KMT2APPARDPPARA
Epoprostenol SCHEMBL16783374 1.00 ALDH1A1 (1.00) ALDH1A1MEN1KMT2APPARDPPARA
Epoprostenol SCHEMBL22607961 1.00 ALDH1A1 (1.00) ALDH1A1MEN1KMT2APPARDPPARA
Epoprostenol SCHEMBL24340812 1.00 ALDH1A1 (1.00) ALDH1A1MEN1KMT2APPARDPPARA
Epoprostenol SCHEMBL705594 1.00 ALDH1A1 (1.00) ALDH1A1MEN1KMT2APPARDPPARA
Epoprostenol SCHEMBL4165739 1.00 ALDH1A1 (1.00) ALDH1A1MEN1KMT2APPARDPPARA
Epoprostenol SCHEMBL24612535 1.00 ALDH1A1 (1.00) ALDH1A1MEN1KMT2APPARDPPARA
Epoprostenol SCHEMBL21283002 1.00 ALDH1A1 (1.00) ALDH1A1MEN1KMT2APPARDPPARA
Epoprostenol SCHEMBL6227411 1.00 ALDH1A1 (1.00) ALDH1A1MEN1KMT2APPARDPPARA

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 2 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11384044-B2 Method for introducing substituent into α,β-unsaturated ketone and method for synthesizing prostaglandin using the same NATIONAL CENTER FOR GERIATRICS AND GERONTOLOGY (JP) 2022-07-12 US disclosed
US-20210355061-A1 METHOD FOR INTRODUCING SUBSTITUENT INTO alpha,beta-UNSATURATED KETONE AND METHOD FOR SYNTHESIZING PROSTAGLANDIN USING THE SAME NATIONAL CENTER FOR GERIATRICS AND GERONTOLOGY (JP) 2021-11-18 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 (2 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-20210355061-A1 METHOD FOR INTRODUCING SUBSTITUENT INTO alpha,beta-UNSATURATED KETONE AND METHOD FOR SYNTHESIZING PROSTAGLANDIN USING THE SAME PTGES, PTGES2, PTGES3 PTGIR 17/4885ALDH1A1 677/4885MEN1 3639/4885
US-11384044-B2 Method for introducing substituent into α,β-unsaturated ketone and method for synthesizing prostaglandin using the same PTGES, PTGES2, PTGES3 PTGIR 16/4885ALDH1A1 618/4885MEN1 3666/4885

“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.