SCHEMBL172607

SCHEMBL172607

CC(C)c1ccc(Oc2ccccc2)cc1

nearest known ligand 0.60

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
LTA4H P09960 6/20 0.57
TSHR P16473 1/20 0.57
MAOA P21397 1/20 0.56
ACACB O00763 2/20 0.50
ACACA Q13085 2/20 0.50
NR1H2 P55055 1/20 0.50
BAX Q07812 1/20 0.50
SRD5A2 P31213 1/20 0.48
FNTA P49354 1/20 0.48
FNTB P49356 1/20 0.48
PTGS1 P23219 1/20 0.47
MEN1 O00255 1/20 0.45
NPC1 O15118 1/20 0.45
RAB9A P51151 1/20 0.45
KMT2A Q03164 1/20 0.45
NLRP3 Q96P20 1/20 0.45
CA1 P00915 1/20 0.45
CA2 P00918 1/20 0.45

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
SCHEMBL20419454 0.94 ACACB (0.58) LTA4HTSHRMAOAACACBACACA
Diphenylether SCHEMBL28334518 0.93 LTA4H (0.60) LTA4HTSHRMAOAACACBACACA
SCHEMBL15849015 0.90 ALDH1A1 (0.48) TSHRMAOAFNTAFNTBMEN1
SCHEMBL4366979 0.90 ALDH1A1 (0.48) TSHRMAOAFNTAFNTBMEN1
Diphenylether SCHEMBL27288324 0.89 HTT (0.52) LTA4HTSHRMAOAACACBACACA
SCHEMBL25969457 0.86 LTA4H (0.57) LTA4HTSHRMAOAACACBACACA
SCHEMBL21120679 0.84 FNTA (0.51) TSHRFNTAFNTBPTGS1MEN1
Bicarbonate SCHEMBL9555855 0.84 RAB9A (0.50) ACACBACACASRD5A2FNTAFNTB
SCHEMBL11858946 0.84 RXRA (0.63) MAOAACACBNPC1RAB9A
SCHEMBL18805968 0.83 ALDH1A1 (0.46) TSHRMAOAACACBACACAFNTA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4922010-A Processes for preparing 2-substituted propionic acid and derivatives thereof UBE INDUSTRIES, LTD. (JP) 1990-05-01 US claimed
US-12018012-B2 Aryl cyclopropyl-amino-isoquinolinyl amide compounds AERIE PHARMACEUTICALS, INC. (US) 2024-06-25 US disclosed
US-12018012-B2 Aryl cyclopropyl-amino-isoquinolinyl amide compounds AERIE PHARMACEUTICALS, INC. (US) 2024-06-25 US disclosed
WO-2024059107-A1 IKZF2 AND CK1-ALPHA DEGRADING COMPOUNDS AND USES THEREOF PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2024-03-21 WO disclosed
EP-3775111-B1 DIARYL ETHERS AS FUEL MARKERS DOW GLOBAL TECHNOLOGIES LLC (US) 2024-03-20 EP disclosed
US-20240024318-A1 SMARCA DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS, INC. 2024-01-25 US disclosed
US-11814338-B2 Pyrazolyl and pyrimidinyl tricyclic enones as antioxidant inflammation modulators REATA PHARMACEUTICALS, INC. (US) 2023-11-14 US disclosed
US-11814338-B2 Pyrazolyl and pyrimidinyl tricyclic enones as antioxidant inflammation modulators REATA PHARMACEUTICALS, INC. (US) 2023-11-14 US disclosed
US-11806335-B2 Heterocyclic carboxylate compounds as glycolate oxidase inhibitors Lilac Therapeutics, Inc. (US) 2023-11-07 US disclosed
US-11806335-B2 Heterocyclic carboxylate compounds as glycolate oxidase inhibitors Lilac Therapeutics, Inc. (US) 2023-11-07 US disclosed
US-7166603-B2 Dihydropyrimidone inhibitors of calcium channel function BRISTOL-MYERS SQUIBB CO. (US) 2007-01-23 US disclosed
US-20070015797-A1 Substituted acid derivatives useful as antidiabetic and antiobesity agents and method CHENG PETER T 2007-01-18 US disclosed
US-7157461-B2 Substituted dihydropyrimidine inhibitors of calcium channel function BRISTOL-MYERS SQUIBB CO. (US) 2007-01-02 US disclosed
US-7157461-B2 Substituted dihydropyrimidine inhibitors of calcium channel function BRISTOL-MYERS SQUIBB CO. (US) 2007-01-02 US disclosed
WO-2005068437-A1 2, 4 - DIAMINOPYRIMIDINES AND THEIR USE FOR INDUCING CARDIOMYOGENESIS NOVARTIS AG (CH) 2005-07-28 WO disclosed
EP-0294220-B1 Photopolymerizable composition HITACHI CHEMICAL CO LTD (JP) 1994-05-25 EP disclosed
US-5034429-A An unsaturated monomer, a photoinitiator and a benzene derivative for providing a cured film HITACHI CHEMICAL CO., LTD. (JP) 1991-07-23 US disclosed
US-4922010-A Processes for preparing 2-substituted propionic acid and derivatives thereof UBE INDUSTRIES, LTD. (JP) 1990-05-01 US disclosed
EP-0294220-A2 Photopolymerizable composition Hitachi Chemical Co., Ltd. (JP) 1988-12-07 EP disclosed
US-4066707-A METHOD FOR MANUFACTURE OF DIPHENOLS AND MONOALKYL ETHERS OF DIPHENOLS AGENCY OF INDUSTRIAL SCIENCE & TECHNOLOGY (JA) 1978-01-03 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-11806335-B2 Heterocyclic carboxylate compounds as glycolate oxidase inhibitors UGDH, PGD, PNPO LTA4H 690/4885TSHR 2776/4885MAOA 75/4885
US-20240024318-A1 SMARCA DEGRADERS AND USES THEREOF SMARCA1, SMARCA2, SMARCC2 LTA4H 3150/4885TSHR 4388/4885MAOA 850/4885
US-12018012-B2 Aryl cyclopropyl-amino-isoquinolinyl amide compounds UACA, HRAS, MYLK LTA4H 3110/4885TSHR 3628/4885MAOA 2392/4885
US-11814338-B2 Pyrazolyl and pyrimidinyl tricyclic enones as antioxidant inflammation modulators GPX4, MPO, GPX1 LTA4H 272/4885TSHR 3603/4885MAOA 1198/4885
US-20070015797-A1 Substituted acid derivatives useful as antidiabetic and antiobesity agents and method GPR119, LIPC, ACACA LTA4H 3219/4885TSHR 780/4885MAOA 407/4885

“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.