SCHEMBL594206

SCHEMBL594206

CC(C)(C)OC(=O)N1CCN(c2ccc([N+](=O)[O-])cc2)CC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
MAPT P10636 8/20 1.00
ALDH1A1 P00352 7/20 1.00
LMNA P02545 2/20 1.00
SMN1; SMN2 Q16637 3/20 0.70
HTT P42858 2/20 0.58
TP53 P04637 1/20 0.58
AKR1C3 P42330 1/20 0.58
SIRT6 Q8N6T7 1/20 0.56
GPR119 Q8TDV5 1/20 0.54
POLB P06746 2/20 0.54
NPC1 O15118 1/20 0.54
RAB9A P51151 1/20 0.54
MEN1 O00255 1/20 0.53
KMT2A Q03164 1/20 0.53

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
SCHEMBL3203878 0.95 MAPT (0.90) MAPTALDH1A1LMNASMN1; SMN2HTT
SCHEMBL3147292 0.94 MAPT (0.88) MAPTALDH1A1LMNASMN1; SMN2HTT
SCHEMBL10035910 0.89 MAPT (0.80) MAPTALDH1A1LMNASMN1; SMN2HTT
SCHEMBL10036432 0.89 MAPT (0.80) MAPTALDH1A1LMNASMN1; SMN2GPR119
SCHEMBL23783084 0.88 MAPT (0.78) MAPTALDH1A1LMNASMN1; SMN2HTT
SCHEMBL30722421 0.88 MAPT (0.78) MAPTALDH1A1LMNASMN1; SMN2GPR119
SCHEMBL8352689 0.88 MAPT (0.78) MAPTALDH1A1LMNASMN1; SMN2GPR119
SCHEMBL5573222 0.87 MAPT (0.76) MAPTALDH1A1LMNASMN1; SMN2HTT
SCHEMBL25845748 0.87 MAPT (0.76) MAPTALDH1A1LMNASMN1; SMN2HTT
SCHEMBL29986023 0.87 MAPT (0.76) MAPTALDH1A1LMNASMN1; SMN2HTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250066389-A1 HETEROCYCLIC AMIDES AND METHODS OF USING THE SAME RGENTA THERAPEUTICS, INC. 2025-02-27 US disclosed
US-20250041429-A1 COMPOUND HAVING BTK PROTEIN DEGRADATION ACTIVITY, AND MEDICAL USES THEREOF UBIX THERAPEUTICS, INC. (KR) 2025-02-06 US disclosed
US-12139492-B2 Substituted pyrimidines for the targeted degradation of Bruton's tyrosine kinase ENDOTARGET INC. 2024-11-12 US disclosed
US-20240360146-A1 BRUTON'S TYROSINE KINASE AND MUTANT DEGRADER, COMPOSITION AND APPLICATION THEREOF SHANGHAI INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF SCIENCES (CN) 2024-10-31 US disclosed
EP-4433457-A1 HETEROCYCLIC AMIDES AND METHODS OF USING THE SAME Rgenta Therapeutics, Inc. (US) 2024-09-25 EP disclosed
EP-4428130-A1 COMPOUND HAVING BTK PROTEIN DEGRADATION ACTIVITY, AND MEDICAL USES THEREOF Ubix Therapeutics, Inc. (KR) 2024-09-11 EP disclosed
US-20240269298-A1 PHOSPHONYL DERIVATIVE, AND COMPOSITION AND PHARMACEUTICAL APPLICATION THEREOF XIZANG HAISCO PHARMACEUTICAL CO., LTD. (CN) 2024-08-15 US disclosed
CN-118271284-A Estrogen receptor modulators and uses thereof 江苏威凯尔医药科技有限公司 2024-07-02 CN disclosed
CN-118159532-A Compound with BTK protein degradation activity and medical application thereof 尤比克斯治疗公司 2024-06-07 CN disclosed
WO-2024117789-A1 PLK1 DEGRADATION INDUCING COMPOUNDS WITH INCREASED RIGIDITY UPPTHERA, INC. (KR) 2024-06-06 WO disclosed
WO-1999021845-A2 4-AMINOTHIAZOLE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS INHIBITORS OF CYCLIN-DEPENDENT KINASES AGOURON PHARMACEUTICALS, INC. (US) 1999-05-06 WO disclosed
EP-0885213-A4 FIBRINOGEN RECEPTOR ANTAGONISTS SMITHKLINE BEECHAM CORP (US) 1999-04-28 EP disclosed
WO-1999004796-A1 FIBRINOGEN RECEPTOR ANTAGONISTS SMITHKLINE BEECHAM CORPORATION (US) 1999-02-04 WO disclosed
EP-0892783-A1 CARBOXYLIC ACID DERIVATIVES WITH AN AGGREGATION-INHIBITING ACTION Dr. Karl Thomae GmbH (DE) 1999-01-27 EP disclosed
EP-0885213-A1 FIBRINOGEN RECEPTOR ANTAGONISTS SMITHKLINE BEECHAM CORPORATION (US) 1998-12-23 EP disclosed
WO-1998035956-A1 HETEROCYCLIC COMPOUNDS USEFUL AS OXIDO-SQUALENE CYCLASE INHIBITORS ZENECA LIMITED (US) 1998-08-20 WO disclosed
WO-1998025617-A1 SUBSTITUTED ARYL PIPERAZINES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY MERCK & CO., INC. (US) 1998-06-18 WO disclosed
WO-1997037975-A1 CARBOXYLIC ACID DERIVATIVES WITH AN AGGREGATION-INHIBITING ACTION DR. KARL THOMAE GMBH (DE) 1997-10-16 WO disclosed
WO-1997025323-A1 FIBRINOGEN RECEPTOR ANTAGONISTS SMITHKLINE BEECHAM CORPORATION (US) 1997-07-17 WO disclosed
US-5556969-A Benzodiazepine derivatives MERCK SHARP & DOHME LTD. (GB) 1996-09-17 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-20240269298-A1 PHOSPHONYL DERIVATIVE, AND COMPOSITION AND PHARMACEUTICAL APPLICATION THEREOF EGFR, BLK, CSNK1A1L MAPT 2478/4885ALDH1A1 4631/4885LMNA 1804/4885
US-12139492-B2 Substituted pyrimidines for the targeted degradation of Bruton's tyrosine kinase BTK, BCL6B, BCL9 MAPT 4237/4885ALDH1A1 3275/4885LMNA 4052/4885
US-20250066389-A1 HETEROCYCLIC AMIDES AND METHODS OF USING THE SAME SNRPA, SF3B5, RBM17 MAPT 3969/4885ALDH1A1 1405/4885LMNA 346/4885
US-20240360146-A1 BRUTON'S TYROSINE KINASE AND MUTANT DEGRADER, COMPOSITION AND APPLICATION THEREOF BTK, ZAP70, SYK MAPT 4559/4885ALDH1A1 4835/4885LMNA 2845/4885
US-20250041429-A1 COMPOUND HAVING BTK PROTEIN DEGRADATION ACTIVITY, AND MEDICAL USES THEREOF BTK, LYN, SYK MAPT 3790/4885ALDH1A1 4704/4885LMNA 4396/4885

“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.