SCHEMBL883026

SCHEMBL883026

CC(C)(OCc1ccccc1)C(=O)O

nearest known ligand 0.57

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
SLC16A3 O15427 8/20 0.55
ALDH1A1 P00352 3/20 0.52
PPARG P37231 5/20 0.50
MCTS1 Q9ULC4 5/20 0.50
SLC16A1 P53985 5/20 0.50
PPARA Q07869 3/20 0.47
PPARD Q03181 1/20 0.47
MAPK1 P28482 1/20 0.46
L3MBTL1 Q9Y468 1/20 0.46
SLC6A2 P23975 1/20 0.46
SLC6A3 Q01959 1/20 0.46
KMT2A Q03164 1/20 0.46
TDP1 Q9NUW8 1/20 0.46

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
SCHEMBL2221138 0.89 SLC16A3 (0.53) SLC16A3PPARGMCTS1SLC16A1
SCHEMBL12223141 0.86 ALDH1A1 (0.55) SLC16A3ALDH1A1PPARGMAPK1L3MBTL1
SCHEMBL6679251 0.85 ALDH1A1 (0.53) SLC16A3ALDH1A1PPARGMCTS1SLC16A1
SCHEMBL11475913 0.84 ALDH1A1 (0.52) ALDH1A1PPARGPPARAMAPK1L3MBTL1
SCHEMBL11344345 0.83 MAOB (0.47) ALDH1A1PPARGMAPK1L3MBTL1SLC6A2
SCHEMBL874424 0.83 ALDH1A1 (0.56) ALDH1A1MAPK1L3MBTL1SLC6A2SLC6A3
SCHEMBL10384205 0.83 SLC6A2 (0.50) SLC16A3ALDH1A1PPARGMAPK1L3MBTL1
SCHEMBL2215266 0.83 RXRA (0.46) SLC16A3ALDH1A1PPARGMCTS1SLC16A1
SCHEMBL2352150 0.83 RXRA (0.46) SLC16A3PPARGMCTS1SLC16A1PPARA
SCHEMBL8935661 0.83 SLC16A3 (0.46) SLC16A3PPARGMCTS1SLC16A1PPARA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026107328-A1 AGONISTS OF PARATHYROID HORMONE 1 AND INCRETIN RECEPTORS SEPTERNA, INC. (US) 2026-05-21 WO disclosed
US-11472810-B2 Imidazopyrazinones as PDE1 inhibitors H. LUNDBECK A/S (DK) 2022-10-18 US disclosed
US-20210238182-A1 IMIDAZOPYRAZINONES AS PDE1 INHIBITORS H. LUNDBECK A/S (DK) 2021-08-05 US disclosed
US-10912773-B2 Combinations comprising substituted imidazo[1,5-a]pyrazinones as PDE1 inhibitors H. LUNDBECK A/S (DK) 2021-02-09 US disclosed
US-10905688-B2 Combinations comprising substituted imidazo[1,5-α]pyrazinones as PDE1 inhibitors H. LUNDBECK A/S (DK) 2021-02-02 US disclosed
US-10858362-B2 Imidazopyrazinones as PDE1 inhibitors H. LUNDBECK A/S (DK) 2020-12-08 US disclosed
EP-3532064-B1 COMBINATION TREATMENTS COMPRISING IMIDAZOPYRAZINONES FOR THE TREATMENT OF PSYCHIATRIC AND/OR COGNITIVE DISORDERS H LUNDBECK AS (DK) 2020-07-29 EP disclosed
US-20190282572-A1 COMBINATION TREATMENTS COMPRISING ADMINISTRATION OF IMIDAZOPYRAZINONES H. LUNDBECKA/S (DK) 2019-09-19 US disclosed
US-20190282571-A1 COMBINATION TREATMENTS COMPRISING ADMINISTRATION OF IMIDAZOPYRAZINONES H. LUNDBECK A/S (DK) 2019-09-19 US disclosed
EP-3532053-A1 COMBINATION TREATMENTS COMPRISING ADMINISTRATION OF IMIDAZOPYRAZINONES H. Lundbeck A/S (DK) 2019-09-04 EP disclosed
CN-1070487-C Hexahydronaphthalene ester derivatives, their preparation and their therapeutic uses SANKYO CO (JP) 2001-09-05 CN disclosed
US-5491167-A INHIBITORS OF CHOLESTEROL BIOSYNTHESIS SANKYO COMPANY, LIMITED (JP) 1996-02-13 US disclosed
CN-1098099-A The hexahydro naphthalene ester derivative, their preparation and their treatment are used SANKYO CO (JP) 1995-02-01 CN disclosed
EP-0609058-A2 Hexahydronaphthalene ester derivatives, their preparation and their therapeutic uses SANKYO COMPANY LIMITED (JP) 1994-08-03 EP disclosed
EP-0201221-B1 6-(1-ACYL-1-HYDROXY METHYL) PENICILLANIC ACID DERIVATIVES PFIZER INC. (US) 1990-08-01 EP disclosed
CN-1003712-B Process for preparing 6- (1-acyl-1-hydroxymethyl or acetoxymethyl) penicillanic acid derivatives 美国辉瑞有限公司 1989-03-29 CN disclosed
US-4762921-A 6-(1-acyl-1-hydroxymethyl)penicillanic acid derivatives PFIZER INC. (US) 1988-08-09 US disclosed
US-4675186-A 6-(1-acyl-1-hydroxymethyl)penicillanic acid derivatives PFIZER INC. (US) 1987-06-23 US disclosed
EP-0201221-A1 6-(1-acyl-1-hydroxy methyl) penicillanic acid derivatives PFIZER INC. (US) 1986-11-12 EP disclosed
CN-86102736-A The preparation method and the application thereof of 6-(1-acyl group-1-methylol) penicillanic acid derivative 1986-10-15 CN 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 (7 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-20190282571-A1 COMBINATION TREATMENTS COMPRISING ADMINISTRATION OF IMIDAZOPYRAZINONES PDE12, PDE1B, PDE1A SLC16A3 4654/4885ALDH1A1 421/4885PPARG 565/4885
US-10858362-B2 Imidazopyrazinones as PDE1 inhibitors PDE12, PDE4A, PDE5A SLC16A3 3720/4885ALDH1A1 110/4885PPARG 973/4885
US-20210238182-A1 IMIDAZOPYRAZINONES AS PDE1 INHIBITORS PDE12, PDE4A, PDE5A SLC16A3 3720/4885ALDH1A1 110/4885PPARG 973/4885
US-11472810-B2 Imidazopyrazinones as PDE1 inhibitors PDE12, PDE4A, PDE5A SLC16A3 3720/4885ALDH1A1 110/4885PPARG 973/4885
US-10912773-B2 Combinations comprising substituted imidazo[1,5-a]pyrazinones as PDE1 inhibitors PDE5A, PDE3A, PDE12 SLC16A3 4387/4885ALDH1A1 151/4885PPARG 1213/4885
US-10905688-B2 Combinations comprising substituted imidazo[1,5-α]pyrazinones as PDE1 inhibitors PDE1A, PDE12, PDE1B SLC16A3 4785/4885ALDH1A1 92/4885PPARG 2143/4885
US-20190282572-A1 COMBINATION TREATMENTS COMPRISING ADMINISTRATION OF IMIDAZOPYRAZINONES PDE12, PDE4A, PDE1A SLC16A3 4026/4885ALDH1A1 602/4885PPARG 770/4885

“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.