SCHEMBL365094

SCHEMBL365094

CC1(C)OB(c2ccnn2C2CCCCO2)OC1(C)C

nearest known ligand 0.43

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
CYP4F2 P78329 4/20 0.43
CYP4A11 Q02928 4/20 0.43
ATR Q13535 13/20 0.36
ALDH1A1 P00352 1/20 0.35
LMNA P02545 1/20 0.35
POLB P06746 1/20 0.35
RXRA P19793 1/20 0.33
RXRB P28702 1/20 0.33
RXRG P48443 1/20 0.33
HCRTR1 O43613 1/20 0.33
HCRTR2 O43614 1/20 0.33

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
SCHEMBL17129377 0.89 CYP4F2 (0.38) CYP4F2CYP4A11ATRALDH1A1LMNA
SCHEMBL24142066 0.86 CYP4F2 (0.41) CYP4F2CYP4A11ATRALDH1A1LMNA
SCHEMBL24031822 0.84 CYP4F2 (0.41) CYP4F2CYP4A11ATRALDH1A1LMNA
SCHEMBL26199501 0.82 CYP4F2 (0.40) CYP4F2CYP4A11ATRALDH1A1LMNA
SCHEMBL24031809 0.82 CYP4F2 (0.43) CYP4F2CYP4A11ATRALDH1A1LMNA
SCHEMBL21759067 0.80 PKM (0.36) ALDH1A1LMNA
SCHEMBL26694018 0.80 CYP4F2 (0.35) CYP4F2CYP4A11ALDH1A1LMNAPOLB
SCHEMBL15388480 0.79 GAA (0.39) CYP4F2CYP4A11ATRALDH1A1LMNA
SCHEMBL18209774 0.79 CYP4F2 (0.35) CYP4F2CYP4A11ATRRXRARXRB
SCHEMBL17501948 0.79 SMN1; SMN2 (0.36) ALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12583840-B2 Method for the preparation of androgen receptor antagonists and intermediates thereof ORION CORPORATION (FI) 2026-03-24 US claimed
WO-2024257116-A1 NOVEL POLYMORPHIC FORMS OF ASCIMINIB AND ITS PHARMACEUTICAL SALTS THEREOF NATCO PHARMA LIMITED (IN) 2024-12-19 WO claimed
CN-118955380-A Pyrazole organic monomer, preparation method thereof, three-dimensional MOF material and application thereof 云南大学 2024-11-15 CN claimed
CN-116041349-B Xanthine compound, preparation method thereof and application thereof in preparation of novel coronavirus 3CL protease inhibitor 吉斯凯(苏州)制药有限公司 2023-10-20 CN claimed
CN-112823158-B Process for preparing 2- [ (3R) -3-methylmorpholin-4-yl ] -4- (1-methyl-1H-pyrazol-5-yl) -8- (1H-pyrazol-5-yl) -1, 7-naphthyridine 拜耳股份有限公司 2023-08-15 CN claimed
US-20230174517-A1 METHOD FOR THE PREPARATION OF ANDROGEN RECEPTOR ANTAGONISTS AND INTERMEDIATES THEREOF ORION CORPORATION (FI) 2023-06-08 US claimed
CN-116041349-A Xanthine compound, preparation method thereof and application thereof in preparation of novel coronavirus 3CL protease inhibitor 吉斯凯(苏州)制药有限公司 2023-05-02 CN claimed
EP-4149938-A1 METHOD FOR THE PREPARATION OF ANDROGEN RECEPTOR ANTAGONISTS AND INTERMEDIATES THEREOF Orion Corporation (FI) 2023-03-22 EP claimed
CN-115605470-A Process for preparing androgen receptor antagonists and intermediates thereof 奥赖恩公司(FI) 2023-01-13 CN claimed
EP-3841101-A1 METHOD FOR PREPARING 2-[(3R)-3-METHYLMORPHOLIN-4-YL]-4-[1-METHYL-1H-PYRAZOL-5-YL)-8-(1H-PYRAZOL-5-YL)-1,7-NAPHTHYRIDINE Bayer Aktiengesellschaft (DE) 2021-06-30 EP claimed
CN-107428695-B Process for preparing androgen receptor antagonists and intermediates thereof 奥赖恩公司 2021-03-16 CN claimed
WO-2020039025-A1 METHOD FOR PREPARING 2-[(3R)-3-METHYLMORPHOLIN-4-YL]-4-[1-METHYL-1H-PYRAZOL-5-YL)-8-(1H-PYRAZOL-5-YL)-1,7-NAPHTHYRIDINE BAYER AKTIENGESELLSCHAFT (DE) 2020-02-27 WO claimed
EP-3280710-B1 PROCESS FOR THE PREPARATION OF ANDROGEN RECEPTOR ANTAGONISTS AND INTERMEDIATES THEREOF ORION CORP (FI) 2020-02-26 EP claimed
US-10189789-B2 Process for the preparation of androgen receptor antagonists and intermediates thereof ORION CORPORATION (FI) 2019-01-29 US claimed
US-20180099938-A1 PROCESS FOR THE PREPARATION OF ANDROGEN RECEPTOR ANTAGONISTS AND INTERMEDIATES THEREOF ORION CORPORATION (FI) 2018-04-12 US claimed
EP-3280710-A1 PROCESS FOR THE PREPARATION OF ANDROGEN RECEPTOR ANTAGONISTS AND INTERMEDIATES THEREOF Orion Corporation (FI) 2018-02-14 EP claimed
WO-2016162604-A1 PROCESS FOR THE PREPARATION OF ANDROGEN RECEPTOR ANTAGONISTS AND INTERMEDIATES THEREOF ORION CORPORATION (FI) 2016-10-13 WO claimed
WO-2026106969-A1 NOVEL INHIBITORS OF INTERLEUKIN RECEPTOR- ASSOCIATED KINASE UNIVERSITY OF ROCHESTER (US) 2026-05-21 WO disclosed
WO-2010010154-A1 3,4-DIARYLPYRAZOLES AS PROTEIN KINASE INHIBITORS NERVIANO MEDICAL SCIENCES S.R.L. (IT) 2010-01-28 WO disclosed
WO-2009152025-A1 IMIDAZOLE DERIVATIVES USEFUL AS INHIBITORS OF FAAH MERCK & CO., INC. (US) 2009-12-17 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 (4 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-20230174517-A1 METHOD FOR THE PREPARATION OF ANDROGEN RECEPTOR ANTAGONISTS AND INTERMEDIATES THEREOF AR, GNRHR, FSHR CYP4F2 354/4885CYP4A11 126/4885ATR 1799/4885
US-20180099938-A1 PROCESS FOR THE PREPARATION OF ANDROGEN RECEPTOR ANTAGONISTS AND INTERMEDIATES THEREOF AR, NR5A1, GNRHR CYP4F2 494/4885CYP4A11 119/4885ATR 2631/4885
US-12583840-B2 Method for the preparation of androgen receptor antagonists and intermediates thereof AR, FSHR, PKD1 CYP4F2 2009/4885CYP4A11 1079/4885ATR 459/4885
US-10189789-B2 Process for the preparation of androgen receptor antagonists and intermediates thereof AR, NR5A1, GNRHR CYP4F2 494/4885CYP4A11 119/4885ATR 2631/4885

“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.