SCHEMBL265514

SCHEMBL265514

CC[C@@H](Cc1ccccc1)C(=O)O

nearest known ligand 0.83

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.83
PPARG P37231 3/20 0.67
CPA1 P15085 7/20 0.66
CPA3 P15088 3/20 0.66
FOLH1 Q04609 3/20 0.66
CPB1 P15086 1/20 0.66
CPB2 Q96IY4 1/20 0.66
SLC1A3 P43003 1/20 0.59
SLC1A2 P43004 1/20 0.59
SLC1A1 P43005 1/20 0.59
PPARD Q03181 1/20 0.57
PPARA Q07869 1/20 0.57
MME P08473 1/20 0.56
NAALAD2 Q9Y3Q0 1/20 0.54

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
SCHEMBL491524 1.00 CYP1A2 (0.83) CYP1A2PPARGCPA1CPA3FOLH1
SCHEMBL265063 1.00 CYP1A2 (0.83) CYP1A2PPARGCPA1CPA3FOLH1
SCHEMBL4664822 0.91 CYP1A2 (1.00) CYP1A2CPA1CPA3FOLH1CPB1
SCHEMBL12493651 0.90 CYP1A2 (0.74) CYP1A2PPARGCPA1CPA3FOLH1
SCHEMBL22115491 0.89 CYP1A2 (0.95) CYP1A2CPA1CPA3FOLH1CPB1
SCHEMBL27291058 0.89 CYP1A2 (0.95) CYP1A2CPA1CPA3FOLH1CPB1
SCHEMBL9875948 0.89 CYP1A2 (0.95) CYP1A2CPA1CPA3FOLH1CPB1
SCHEMBL4886609 0.88 CYP1A2 (0.69) CYP1A2PPARGCPA1CPA3FOLH1
SCHEMBL21895912 0.86 CYP1A2 (0.67) CYP1A2PPARGCPA1CPA3FOLH1
SCHEMBL11634382 0.86 CYP1A2 (0.67) CYP1A2PPARGCPA1CPA3FOLH1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260007672-A1 INHIBITORS OF MPTP NRG THERAPEUTICS LTD (GB) 2026-01-08 US disclosed
US-12491185-B2 Inhibitors of mPTP NRG THERAPEUTICS LTD (GB) 2025-12-09 US disclosed
EP-4652162-A1 INHIBITORS OF MPTP NRG Therapeutics LTD (GB) 2025-11-26 EP disclosed
US-20250177397-A1 INHIBITORS OF MPTP NRG THERAPEUTICS LTD (GB) 2025-06-05 US disclosed
WO-2024153946-A1 INHIBITORS OF MPTP NRG THERAPEUTICS LTD (GB) 2024-07-25 WO disclosed
US-20240024410-A1 THREE-DIMENTIONAL SURFACE FOR PROTEIN AND SMALL MOLECULE MICROARRAYS THE JOHNS HOPKINS UNIVERSITY 2024-01-25 US disclosed
US-11793855-B2 TFPI inhibitors and methods of use TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2023-10-24 US disclosed
US-11708391-B2 Rapaglutins, novel inhibitors of GLUT and use thereof THE JOHNS HOPKINS UNIVERSITY (US) 2023-07-25 US disclosed
US-20180155399-A1 TFPI INHIBITORS AND METHODS OF USE Baxalta GmbH (CH) 2018-06-07 US disclosed
US-20180072784-A1 TFPI INHIBITORS AND METHODS OF USE Baxalta GmbH (CH) 2018-03-15 US disclosed
US-20090197834-A1 QUINOLONE DERIVATIVE OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF ASTELLAS PHARMA INC. (JP) 2009-08-06 US disclosed
US-20090062366-A1 Pyrrolidine derivative or salt thereof ASTELLAS PHARAMA INC. (JP) 2009-03-05 US disclosed
US-20090062366-A1 Pyrrolidine derivative or salt thereof ASTELLAS PHARAMA INC. (JP) 2009-03-05 US disclosed
WO-2008002449-A2 GLYCOMIMETIC INHIBITORS OF SIGLEC-8 GLYCOMIMETICS, INC. (US) 2008-01-03 WO disclosed
EP-1203770-B1 Pyran-2-ones and 5,6-dihydropyran-2-ones useful for treating hyperplasia and other diseases UPJOHN CO (US) 2005-03-09 EP disclosed
EP-0668860-B1 PYRAN-2-ONES AND 5,6-DIHYDROPYRAN-2-ONES USEFUL FOR TREATING HIV AND OTHER RETROVIRUSES UPJOHN CO (US) 2002-09-11 EP disclosed
EP-1203770-A1 Pyran-2-ones and 5,6-dihydropyran-2-ones useful for treating hyperplasia and other diseases PHARMACIA & UPJOHN COMPANY (US) 2002-05-08 EP disclosed
US-6365398-B1 REACTING RACEMIC CARBOXYLIC ACID ESTER WITH RACEMIC ALCOHOL IN PRESENCE OF A CARBOXYL ESTER HYDROLASE BASF AKTIENGESELLSCHAFT (DE) 2002-04-02 US disclosed
EP-0668860-A1 PYRAN-2-ONES AND 5,6-DIHYDROPYRAN-2-ONES USEFUL FOR TREATING HIV AND OTHER RETROVIRUSES PHARMACIA & UPJOHN COMPANY (US) 1995-08-30 EP disclosed
WO-1994011361-A1 PYRAN-2-ONES AND 5,6-DIHYDROPYRAN-2-ONES USEFUL FOR TREATING HIV AND OTHER RETROVIRUSES THE UPJOHN COMPANY (US) 1994-05-26 WO 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 (10 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-20180072784-A1 TFPI INHIBITORS AND METHODS OF USE TFPI, TFPI2, SERPINC1 CYP1A2 4247/4885PPARG 4775/4885CPA1 82/4885
US-11708391-B2 Rapaglutins, novel inhibitors of GLUT and use thereof SLC2A1, SLC2A4, SLC2A2 CYP1A2 3807/4885PPARG 906/4885CPA1 3224/4885
US-12491185-B2 Inhibitors of mPTP PARK7, PINK1, SNCA CYP1A2 378/4885PPARG 2030/4885CPA1 2386/4885
US-20090062366-A1 Pyrrolidine derivative or salt thereof CASR, CYP2R1, PTH1R CYP1A2 1088/4885PPARG 509/4885CPA1 745/4885
US-20180155399-A1 TFPI INHIBITORS AND METHODS OF USE TFPI, TFPI2, F13B CYP1A2 4351/4885PPARG 4746/4885CPA1 81/4885
US-20240024410-A1 THREE-DIMENTIONAL SURFACE FOR PROTEIN AND SMALL MOLECULE MICROARRAYS MRPS23, CD2BP2, MRPL21 CYP1A2 4720/4885PPARG 4600/4885CPA1 2868/4885
US-20250177397-A1 INHIBITORS OF MPTP PARK7, PINK1, SNCA CYP1A2 378/4885PPARG 2030/4885CPA1 2386/4885
US-11793855-B2 TFPI inhibitors and methods of use TFPI, TFPI2, F3 CYP1A2 4346/4885PPARG 4779/4885CPA1 77/4885
US-20090197834-A1 QUINOLONE DERIVATIVE OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF P2RY12, P2RY11, P2RY10 CYP1A2 2147/4885PPARG 2451/4885CPA1 2108/4885
US-20260007672-A1 INHIBITORS OF MPTP PARK7, SNCA, CYC1 CYP1A2 1009/4885PPARG 3056/4885CPA1 1018/4885

“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.