Dimethylcurcumin

Dimethylcurcumin

SCHEMBL3487103

COc1ccc(/C=C/C(=O)/C=C(O)/C=C/c2ccc(OC)c(OC)c2)cc1OC

nearest known ligand 0.78

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

AR

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HDAC1 Q13547 3/20 0.78
HDAC2 Q92769 3/20 0.78
HDAC8 Q9BY41 3/20 0.78
KDM4E B2RXH2 1/20 0.71
ALDH1A1 P00352 1/20 0.71
HPGD P15428 1/20 0.71
ALOX15 P16050 1/20 0.71
MAPK1 P28482 1/20 0.71
SMN1; SMN2 Q16637 1/20 0.71
HSD17B10 Q99714 1/20 0.71
GSK3B P49841 3/20 0.70
BACE1 P56817 2/20 0.69
NFE2L2 Q16236 2/20 0.65
JUN P05412 3/20 0.64
NFKB1 P19838 2/20 0.64
KMT2A Q03164 2/20 0.63
ABCG2 Q9UNQ0 2/20 0.63
MEN1 O00255 1/20 0.63
FOS P01100 1/20 0.62
CYP1A2 P05177 1/20 0.60

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
Dimethylcurcumin SCHEMBL3686107 1.00 HDAC1 (0.78) HDAC1HDAC2HDAC8KDM4EALDH1A1
Dimethylcurcumin SCHEMBL3487105 1.00 HDAC1 (0.78) HDAC1HDAC2HDAC8KDM4EALDH1A1
Dimethylcurcumin SCHEMBL29354872 1.00 HDAC1 (0.78) HDAC1HDAC2HDAC8KDM4EALDH1A1
SCHEMBL14112832 0.93 HDAC1 (0.69) HDAC1HDAC2HDAC8KDM4EALDH1A1
SCHEMBL16888009 0.93 GSK3B (0.81) HDAC1HDAC2HDAC8KDM4EALDH1A1
Dimethylcurcumin SCHEMBL2528943 0.93 HDAC1 (0.69) HDAC1HDAC2HDAC8KDM4EALDH1A1
Dimethylcurcumin SCHEMBL2528940 0.93 HDAC1 (0.69) HDAC1HDAC2HDAC8KDM4EALDH1A1
Methylcurcumin SCHEMBL9907002 0.93 GSK3B (0.81) HDAC1HDAC2HDAC8KDM4EALDH1A1
SCHEMBL21743109 0.93 HDAC1 (0.71) HDAC1HDAC2HDAC8KDM4EALDH1A1
SCHEMBL9907006 0.92 HDAC1 (0.67) HDAC1HDAC2HDAC8KDM4EALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114903902-A Application of GnRH receptor antagonist and androgen receptor antagonist in preparation of medicine for treating prostatic cancer 江苏恒瑞医药股份有限公司 2022-08-16 CN claimed
US-20180008557-A1 USE OF TWO BOTANICALS WITH COMPLEMENTARY ACTIVITIES FOR IMPROVEMENT OF SKIN THE REGENTS OF THE UNIVERSITY OF MICHIGAN 2018-01-11 US claimed
US-20100105644-A1 BOTANICAL COMPOSITION FOR ENHANCED SKIN REPAIR AND USES THEREOF THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2010-04-29 US claimed
US-20100048676-A1 Non-androgen dependent roles for androgen receptor in liver cancer UNIVERSITY OF ROCHESTER (US) 2010-02-25 US claimed
US-12630883-B2 Test method of dividing blastic plasmacytoid dendritic cell neoplasm (BPDCN) into subtypes JAPANESE FOUNDATION FOR CANCER RESEARCH (JP) 2026-05-19 US disclosed
US-20250339385-A1 TOPICAL FORMULATION OF DIMETHYLCURCUMIN Annji Pharmaceutical Co., Ltd. (TW) 2025-11-06 US disclosed
US-12303470-B2 Method and composition for selective treatment of androgen receptors SKINQRI, LLC (US) 2025-05-20 US disclosed
EP-4330222-A4 TOPICAL FORMULATION OF DIMETHYLCURCUMIN Annji Pharmaceutical Co., Ltd. (TW) 2025-04-09 EP disclosed
EP-3413045-B1 DIAGNOSIS MARKER FOR RARE HEMATOPOIETIC TUMOR, TEST METHOD, THERAPEUTIC AGENT, AND SCREENING METHOD JAPANESE FOUND FOR CANCER RES (JP) 2024-04-03 EP disclosed
EP-4330222-A1 TOPICAL FORMULATION OF DIMETHYLCURCUMIN Annji Pharmaceutical Co., Ltd. (TW) 2024-03-06 EP disclosed
US-11802113-B2 Substituted pyrazole compounds, compositions containing same, and use thereof SHENZHEN TARGETRX, INC. (CN) 2023-10-31 US disclosed
US-20230323475-A1 TEST METHOD, OF DIVIDING BLASTIC PLASMACYTOID DENDRITIC CELL NEOPLASM (BPDCN) INTO SUBTYPES JAPANESE FOUNDATION FOR CANCER RESEARCH (JP) 2023-10-12 US disclosed
EP-1804806-A2 METHODS AND COMPOSITIONS FOR ENHANCING DEGRADATION OF NUCLEAR RECEPTOR TRANSCRIPTION FACTORS AND USES THEREOF AndroScience Corporation (US) 2007-07-11 EP disclosed
EP-1765346-A2 ENHANCEMENT OF ANTI-ANDROGENIC ACTIVITY BY A COMBINATION OF INHIBITORS TARGETING DIFFERENT STEPS OF A STEROID-DEPENDENT GENE ACTIVATION PATHWAY AND USES THEREOF AndroScience Corporation (US) 2007-03-28 EP disclosed
US-20070060644-A1 Therapeutic curcumin derivatives STC.UNM 2007-03-15 US disclosed
US-20070060644-A1 Therapeutic curcumin derivatives STC.UNM 2007-03-15 US disclosed
US-20060084704-A1 Methods and compositions for enhancing degradation of nuclear receptor transcription factors and uses thereof ANDROSCIENCE CORPORATION 2006-04-20 US disclosed
WO-2006029040-A2 METHODS AND COMPOSITIONS FOR ENHANCING DEGRADATION OF NUCLEAR RECEPTOR TRANSCRIPTION FACTORS AND USES THEREOF SHIH CHARLES C Y (US) 2006-03-16 WO disclosed
US-20050209205-A1 Enhancement of anti-androgenic activity by a combination of inhibitors targeting different steps of a steroid-dependent gene activation pathway and uses thereof ANDROSCIENCE CORPORATION 2005-09-22 US disclosed
WO-2005072462-A2 ENHANCEMENT OF ANTI-ANDROGENIC ACTIVITY BY A COMBINATION OF INHIBITORS TARGETING DIFFERENT STEPS OF A STEROID-DEPENDENT GENE ACTIVATION PATHWAY AND USES THEREOF SHIH CHARLES (US) 2005-08-11 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 (8 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-20050209205-A1 Enhancement of anti-androgenic activity by a combination of inhibitors targeting different steps of a steroid-dependent gene activation pathway and uses thereof NR5A1, CYP17A1, ESRRB HDAC1 548/4885HDAC2 1274/4885HDAC8 174/4885
US-20180008557-A1 USE OF TWO BOTANICALS WITH COMPLEMENTARY ACTIVITIES FOR IMPROVEMENT OF SKIN CUTA, COL14A1, EBP HDAC1 755/4885HDAC2 1876/4885HDAC8 1371/4885
US-20250339385-A1 TOPICAL FORMULATION OF DIMETHYLCURCUMIN DPM1, DIMT1, DSG1 HDAC1 1146/4885HDAC2 1151/4885HDAC8 928/4885
US-20070060644-A1 Therapeutic curcumin derivatives FABP2, GLS2, FABP1 HDAC1 345/4885HDAC2 608/4885HDAC8 521/4885
US-12303470-B2 Method and composition for selective treatment of androgen receptors AR, ARNT, SHBG HDAC1 851/4885HDAC2 2542/4885HDAC8 1438/4885
US-11802113-B2 Substituted pyrazole compounds, compositions containing same, and use thereof AR, NR5A1, SRD5A1 HDAC1 144/4885HDAC2 282/4885HDAC8 197/4885
US-12630883-B2 Test method of dividing blastic plasmacytoid dendritic cell neoplasm (BPDCN) into subtypes BCL3, BRD4, BCL6 HDAC1 473/4885HDAC2 207/4885HDAC8 43/4885
US-20100105644-A1 BOTANICAL COMPOSITION FOR ENHANCED SKIN REPAIR AND USES THEREOF CUTA, COL14A1, BACH1 HDAC1 425/4885HDAC2 1794/4885HDAC8 1072/4885

“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.