Hydroxytoluic Acid

Hydroxytoluic Acid

SCHEMBL1333592

Cc1cccc(C(=O)[O-])c1O.[Cu+]

nearest known ligand 0.64

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.64
KDM4E B2RXH2 4/20 0.64
HPGD P15428 3/20 0.64
HSD17B10 Q99714 1/20 0.64
KMT2A Q03164 2/20 0.55
CYP3A4 P08684 1/20 0.55
CYP2C9 P11712 1/20 0.55
TRPA1 O75762 1/20 0.46
NPC1 O15118 3/20 0.46
RAB9A P51151 3/20 0.46
HTT P42858 1/20 0.46
SMN1; SMN2 Q16637 1/20 0.46
GAA P10253 2/20 0.44
MAPT P10636 1/20 0.44
PLAU P00749 2/20 0.43
F2 P00734 1/20 0.43
F10 P00742 1/20 0.43
PLG P00747 1/20 0.43
PLAT P00750 1/20 0.43
KLK1 P06870 1/20 0.43

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
Hydroxytoluic Acid SCHEMBL29380596 1.00 ALDH1A1 (0.64) ALDH1A1KDM4EHPGDHSD17B10KMT2A
Hydroxytoluic Acid SCHEMBL29975592 0.96 ALDH1A1 (0.64) ALDH1A1KDM4EHPGDHSD17B10KMT2A
Hydroxytoluic Acid SCHEMBL622891 0.96 ALDH1A1 (0.64) ALDH1A1KDM4EHPGDHSD17B10KMT2A
Hydroxytoluic Acid SCHEMBL31175008 0.96 ALDH1A1 (0.64) ALDH1A1KDM4EHPGDHSD17B10KMT2A
Hydroxytoluic Acid SCHEMBL29975360 0.96 ALDH1A1 (0.64) ALDH1A1KDM4EHPGDHSD17B10KMT2A
Hydroxytoluic Acid SCHEMBL9418192 0.96 ALDH1A1 (0.64) ALDH1A1KDM4EHPGDHSD17B10KMT2A
Hydroxytoluic Acid SCHEMBL29975309 0.96 ALDH1A1 (0.64) ALDH1A1KDM4EHPGDHSD17B10KMT2A
Hydroxytoluic Acid SCHEMBL416477 0.96 ALDH1A1 (0.64) ALDH1A1KDM4EHPGDHSD17B10KMT2A
Hydroxytoluic Acid SCHEMBL4389834 0.96 ALDH1A1 (0.64) ALDH1A1KDM4EHPGDHSD17B10KMT2A
Hydroxytoluic Acid SCHEMBL8929635 0.87 ALDH1A1 (0.69) ALDH1A1KDM4EHPGDHSD17B10KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4613745-A2 PROCESS FOR PREPARING A COT INHIBITOR COMPOUND Gilead Sciences, Inc. (US) 2025-09-10 EP claimed
CN-119661545-A Preparation method and application of metal phthalocyanine compound with high-efficiency photothermal conversion capability 浙江理工大学 2025-03-21 CN claimed
CN-115397824-B Process for preparing COT inhibitor compounds 吉利德科学公司 2024-10-22 CN claimed
CN-117024354-B Preparation method of Rui Mi Buti Ni 天津凯莱英制药有限公司 2023-12-08 CN claimed
CN-117164875-A Preparation method of tubular metal copper phthalocyanine polymer and cyclic carbonate 浙江理工大学 2023-12-05 CN claimed
CN-117024354-A Preparation method of Rui Mi Buti Ni 天津凯莱英制药有限公司 2023-11-10 CN claimed
CN-114989399-B Room temperature Suzuki cross-coupling polymerization method of conjugated polymer semiconductor material 中国科学院大学 2023-08-01 CN claimed
EP-4126862-A1 PROCESS FOR PREPARING A COT INHIBITOR COMPOUND GILEAD SCIENCES, INC. (US) 2023-02-08 EP claimed
CN-115397824-A Process for preparing COT inhibitor compounds 吉利德科学公司 2022-11-25 CN claimed
WO-2021202688-A1 PROCESS FOR PREPARING A COT INHIBITOR COMPOUND GILEAD SCIENCES, INC. (US) 2021-10-07 WO claimed
US-20100197954-A1 SYNTHESIS OF SPHINGOSINES AND THEIR DERIVATIVES NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2010-08-05 US claimed
WO-2008030840-A2 SYNTHESIS OF SPHINGOSINES AND THEIR DERIVATIVES EMORY UNIVERSITY (US) 2008-03-13 WO claimed
US-12617789-B2 Small molecular inhibitors of NF-κb inducing kinase JANSSEN PHARMACEUTICA NV (BE) 2026-05-05 US disclosed
EP-4724070-A2 WRN INHIBITORS Nimbus Wadjet, Inc. (US) 2026-04-15 EP disclosed
US-12600717-B2 Tricyclic compounds as inhibitors of KRAS INCYTE CORPORATION (US) 2026-04-14 US disclosed
US-12528806-B2 WRN inhibitors NIMBUS WADJET, INC. (US) 2026-01-20 US disclosed
WO-2010090767-A2 ENHANCING BIOCOMPATIBILITY OF A MEDICAL DEVICE ST. JUDE MEDICAL, INC. (US) 2010-08-12 WO disclosed
WO-2010085547-A2 METHODS OF PREPARING 1-DEOXY-SPHINGOID BASES AND DERIVATIVES THEREOF EMORY UNIVERSITY (US) 2010-07-29 WO disclosed
US-6969716-B2 5-phenyl[1,2,4]triazines as ligands for GABA-A α2/α3 receptors for treating anxiety or depression MERCK SHARP & DOHME LTD. 2005-11-29 US disclosed
US-20040192692-A1 5-Phenyl[1,2,4]triazines as ligands for GABA-A alpha2/alpha3 receptors for treating anxiety or depression MERCK SHARP & DOHME, LTD. (GB) 2004-09-30 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-12600717-B2 Tricyclic compounds as inhibitors of KRAS KRAS, NRAS, HRAS ALDH1A1 2111/4885KDM4E 3998/4885HPGD 2720/4885
US-20040192692-A1 5-Phenyl[1,2,4]triazines as ligands for GABA-A alpha2/alpha3 receptors for treating anxiety or depression GABRA1, GABRA5, GABRA2 ALDH1A1 260/4885KDM4E 3163/4885HPGD 1721/4885
US-12617789-B2 Small molecular inhibitors of NF-κb inducing kinase IRAK3, IKBKB, IKBKG ALDH1A1 3824/4885KDM4E 1798/4885HPGD 1972/4885
US-12528806-B2 WRN inhibitors WRN, RECQL, BLM ALDH1A1 1817/4885KDM4E 1099/4885HPGD 1748/4885
US-20100197954-A1 SYNTHESIS OF SPHINGOSINES AND THEIR DERIVATIVES SPHK1, SPHK2, S1PR2 ALDH1A1 2912/4885KDM4E 1397/4885HPGD 2038/4885

“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.