Beraprost

Beraprost

SCHEMBL16904620

CC#CCC(C)[C@H](O)/C=C/[C@@H]1[C@H]2c3cccc(CCCC(=O)O)c3O[C@H]2C[C@H]1O

nearest known ligand 0.85

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PTGIR

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

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
▸ PTGIR known ✓ P43119 4/20 0.85
▸ PTGER3 P43115 13/20 0.53
▸ PTGER2 P43116 3/20 0.53
▸ PTGER1 P34995 1/20 0.53
▸ PTGDR Q13258 1/20 0.53
▸ PTGER4 P35408 3/20 0.39
▸ PTGFR P43088 12/20 0.37
▸ ALDH1A1 P00352 1/20 0.36
▸ TBXA2R P21731 1/20 0.34
▸ KCNH2 Q12809 1/20 0.34

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
Beraprost SCHEMBL4754472 1.00 PTGIR (0.85) PTGIRPTGER3PTGER2PTGER1PTGDR
Beraprost SCHEMBL11946708 1.00 PTGIR (0.85) PTGIRPTGER3PTGER2PTGER1PTGDR
Beraprost SCHEMBL1554142 1.00 PTGIR (0.85) PTGIRPTGER3PTGER2PTGER1PTGDR
Beraprost SCHEMBL4754473 1.00 PTGIR (0.85) PTGIRPTGER3PTGER2PTGER1PTGDR
Beraprost SCHEMBL16405382 1.00 PTGIR (0.85) PTGIRPTGER3PTGER2PTGER1PTGDR
Beraprost SCHEMBL6084946 1.00 PTGIR (0.85) PTGIRPTGER3PTGER2PTGER1PTGDR
Beraprost SCHEMBL16894023 1.00 PTGIR (0.85) PTGIRPTGER3PTGER2PTGER1PTGDR
Beraprost SCHEMBL22972690 1.00 PTGIR (0.85) PTGIRPTGER3PTGER2PTGER1PTGDR
Beraprost SCHEMBL21778834 1.00 PTGIR (0.85) PTGIRPTGER3PTGER2PTGER1PTGDR
Beraprost SCHEMBL19113984 1.00 PTGIR (0.85) PTGIRPTGER3PTGER2PTGER1PTGDR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240082154-A1 DISEASE-SITE-SPECIFIC LIPOSOMAL FORMULATION CUORIPS INC. (JP) 2024-03-14 — — US claimed
US-20210113464-A1 DISEASE-SITE-SPECIFIC LIPOSOMAL FORMULATION CUORIPS INC. (JP) 2021-04-22 — — US claimed
EP-3718537-A1 DISEASE-SITE-SPECIFIC LIPOSOMAL FORMULATION Osaka University (JP) 2020-10-07 — — EP claimed
US-20160250395-A1 DRUG-ELUTING STENT GRAFT ONO PHARMACEUTICAL CO., LTD. (JP) 2016-09-01 — — US claimed
US-20240082154-A1 DISEASE-SITE-SPECIFIC LIPOSOMAL FORMULATION CUORIPS INC. (JP) 2024-03-14 — — US disclosed
WO-2023088497-A2 NITRIC OXIDE DONOR TYPE BERAPROST DERIVATIVE AND PHARMACEUTICAL COMPOSITION AND USE THEREOF 广州楷石医药有限公司 2023-05-25 — — WO disclosed
US-20230002339-A1 PROCESSES AND INTERMEDIATES FOR THE PREPARATIONS OF BENZOPROSTACYCLIN ANALOGUES AND BENZOPROSTACYCLIN ANALOGUES PREPARED THEREFROM CHIROGATE INTERNATIONAL INC. (TW) 2023-01-05 — — US disclosed
EP-4098651-A1 PROCESS FOR THE PREPARATION OF BERAPROST OR SIMILAR BENZOPROSTACYCLIN ANALOGUES STARTING FROM 2-(3-BROMO-2-FLUOROPHENYL)-4-HYDROXYCYCLOPENT-2-ENONE OR SIMILAR REACTANTS Chirogate International Inc. (TW) 2022-12-07 — — EP disclosed
CN-115433071-A Methods and intermediates for preparing benzoprostacyclin analogs, and benzoprostacyclin analogs prepared therefrom 佳和桂科技股份有限公司 2022-12-06 — — CN disclosed
US-20210113464-A1 DISEASE-SITE-SPECIFIC LIPOSOMAL FORMULATION CUORIPS INC. (JP) 2021-04-22 — — US disclosed
EP-3718537-A1 DISEASE-SITE-SPECIFIC LIPOSOMAL FORMULATION Osaka University (JP) 2020-10-07 — — EP disclosed
US-20200171026-A1 PROSTACYCLIN RECEPTOR AGONISTS FOR REDUCTION OF BODY FAT ALLERGAN INC (US) 2020-06-04 — — US disclosed
US-8980944-B2 EP2 and EP4 agonists as agents for the treatment of influenza a viral infection GEMMUS PHARMA INC. (US) 2015-03-17 — — US disclosed
US-8957240-B2 Method for the purification of prostaglandins JOHNSON MATTHEY PUBLIC LIMITED COMPANY (GB) 2015-02-17 — — US disclosed
US-8519178-B2 Method for the purification of prostaglandins JOHNSON MATTHEY PUBLIC LIMITED COMPANY (GB) 2013-08-27 — — US disclosed
US-8519178-B2 Method for the purification of prostaglandins JOHNSON MATTHEY PUBLIC LIMITED COMPANY (GB) 2013-08-27 — — US disclosed
US-8183286-B2 EP2 and EP4 agonists as agents for the treatment of influenza a viral infection GEMMUS PHARMA INC. (US) 2012-05-22 — — US disclosed
US-20100324313-A1 METHOD FOR THE PURIFICATION OF PROSTAGLANDINS JOHNSON MATTHEY PUBLIC LIMITED COMPANY (GB) 2010-12-23 — — US disclosed
US-20090170931-A1 EP2 and EP4 agonists as agents for the treatment of influenza a viral infection BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2009-07-02 — — US disclosed
US-7345181-B2 Process for preparing prostaglandin derivatives and starting materials for the same YONSUNG FINE CHEMICAL CO., LTD. (KR) 2008-03-18 — — 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 (6 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-20200171026-A1 PROSTACYCLIN RECEPTOR AGONISTS FOR REDUCTION OF BODY FAT PTGIR, PTGER1, PTGDR PTGIR 1/4885PTGER3 10/4885PTGER2 5/4885
US-20090170931-A1 EP2 and EP4 agonists as agents for the treatment of influenza a viral infection PTGER4, PTGER2, PTGER1 PTGIR 11/4885PTGER3 4/4885PTGER2 2/4885
US-20210113464-A1 DISEASE-SITE-SPECIFIC LIPOSOMAL FORMULATION PTGDR2, PLA2R1, PTGDR PTGIR 7/4885PTGER3 40/4885PTGER2 13/4885
US-20230002339-A1 PROCESSES AND INTERMEDIATES FOR THE PREPARATIONS OF BENZOPROSTACYCLIN ANALOGUES AND BENZOPROSTACYCLIN ANALOGUES PREPARED THEREFROM PTGIS, PTGIR, PTGES PTGIR 2/4885PTGER3 24/4885PTGER2 16/4885
US-20240082154-A1 DISEASE-SITE-SPECIFIC LIPOSOMAL FORMULATION LPAR2, PLA2R1, PTGDR2 PTGIR 10/4885PTGER3 44/4885PTGER2 12/4885
US-20100324313-A1 METHOD FOR THE PURIFICATION OF PROSTAGLANDINS PTGES, PTGES2, PTGS2 PTGIR 9/4885PTGER3 6/4885PTGER2 7/4885

“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.

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