SCHEMBL572174

SCHEMBL572174

CC(C)(O)C1CCNCC1

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.43
MEN1 O00255 1/20 0.43
CYP2D6 P10635 1/20 0.43
HRH1 P35367 1/20 0.43
SCN1A P35498 1/20 0.43
KMT2A Q03164 1/20 0.43
SCN2A Q99250 1/20 0.43
SCN3A Q9NY46 1/20 0.43
GABRA1 P14867 2/20 0.35
TSHR P16473 2/20 0.35
GABRG2 P18507 2/20 0.35
GABRB3 P28472 2/20 0.35
GABRA5 P31644 2/20 0.35
GABRA3 P34903 2/20 0.35
GABRA2 P47869 2/20 0.35
GABRA6 Q16445 2/20 0.35
GABRP O00591 1/20 0.35
GABRD O14764 1/20 0.35
GABRB1 P18505 1/20 0.35
GABRB2 P47870 1/20 0.35

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
Hydrochloric Acid SCHEMBL28461176 0.97 LMNA (0.42) LMNAMEN1CYP2D6HRH1SCN1A
SCHEMBL15667904 0.84
SCHEMBL15667935 0.84
SCHEMBL2485059 0.84
Hydrochloric Acid SCHEMBL25315391 0.82 LMNA (0.35) LMNAMEN1CYP2D6HRH1SCN1A
Hydrochloric Acid SCHEMBL571900 0.82 LMNA (0.35) LMNAMEN1CYP2D6HRH1SCN1A
Hydrochloric Acid SCHEMBL30218279 0.82 LMNA (0.35) LMNAMEN1CYP2D6HRH1SCN1A
Hydrochloric Acid SCHEMBL16600271 0.82 LMNA (0.35) LMNAMEN1CYP2D6HRH1SCN1A
SCHEMBL14246961 0.81 LMNA (0.42) LMNAMEN1CYP2D6HRH1SCN1A
SCHEMBL27925056 0.81 LMNA (0.42) LMNAMEN1CYP2D6HRH1SCN1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111606842-A Preparation method of 2- (4-piperidyl) -2-propanol and hydrochloride thereof 安徽中羰碳一工业技术有限责任公司 2020-09-01 CN claimed
CN-106366093-B Fused ring pyrimidine compound, intermediate, preparation method, composition and application thereof 广州再极医药科技有限公司 2020-08-18 CN claimed
US-10494378-B2 Fused ring pyrimidine compound, intermediate, and preparation method, composition and use thereof GUANGZHOU MAXINOVEL PHARMACEUTICALS CO., LTD. (CN) 2019-12-03 US claimed
EP-3354653-B1 FUSED RING PYRIMIDINE COMPOUND, INTERMEDIATE, AND PREPARATION METHOD, COMPOSITION AND USE THEREOF GUANGZHOU MAXINOVEL PHARMACEUTICALS CO LTD (CN) 2019-09-04 EP claimed
EP-3354653-A1 FUSED RING PYRIMIDINE COMPOUND, INTERMEDIATE, AND PREPARATION METHOD, COMPOSITION AND USE THEREOF Guangzhou Maxinovel Pharmaceuticals Co. Ltd. (CN) 2018-08-01 EP claimed
US-20180208604-A1 FUSED RING PYRIMIDINE COMPOUND, INTERMEDIATE, AND PREPARATION METHOD, COMPOSITION AND USE THEREOF GUANGZHOU MAXINOVEL PHARMACEUTICALS CO., LTD. (CN) 2018-07-26 US claimed
CN-106366093-A Fused pyrimidine compound, and intermediate, preparation method, composition and application of 广州再极医药科技有限公司 2017-02-01 CN claimed
EP-4027995-B1 HPK1 ANTAGONISTS AND USES THEREOF NIMBUS SATURN INC (US) 2026-05-27 EP disclosed
WO-2026100508-A1 RESIN COMPOSITION, CURED PRODUCT, LAMINATE, METHOD FOR PRODUCING CURED PRODUCT, METHOD FOR PRODUCING LAMINATE, METHOD FOR PRODUCING SEMICONDUCTOR DEVICE, SEMICONDUCTOR DEVICE, AND RESIN 富士フイルム株式会社 2026-05-15 WO disclosed
EP-4739682-A1 1,6-NAPHTHRIDINE COMPOUNDS AS SMARCA2 INHIBITORS USEFUL FOR THE TREATMENT OF SMARCA4 DEFICIENT CANCERS Janssen Pharmaceutica NV (BE) 2026-05-13 EP disclosed
EP-4737451-A1 NOVEL CARBOXAMIDE DERIVATIVE COMPOUND AND PHARMACEUTICAL COMPOSITION COMPRISING SAME Dong Wha Pharm. Co., Ltd. (KR) 2026-05-06 EP disclosed
US-20260099093-A1 PHOTOSENSITIVE RESIN COMPOSITION, METHOD FOR PRODUCING CURED RELIEF PATTERN USING SAME, AND METHOD FOR PRODUCING POLYIMIDE FILM USING SAME ASAHI KASEI KABUSHIKI KAISHA (JP) 2026-04-09 US disclosed
EP-4722211-A1 FGFR2/3 SELECTIVE INHIBITOR, PHARMACEUTICAL COMPOSITION AND USE THEREOF Changchun Genescience Pharmaceutical Co., Ltd. (CN) 2026-04-08 EP disclosed
EP-1456200-A1 LACTAMS AS TACHYKININ ANTAGONISTS Pfizer Limited (GB) 2004-09-15 EP disclosed
WO-2003051868-A1 LACTAMS AS TACHYKININ ANTAGONISTS PFIZER LIMITED (GB) 2003-06-26 WO disclosed
EP-0625509-B1 N-alkyl substituted piperidine-derivatives with neurokinin receptor antagonist activity ZENECA LTD (GB) 1997-07-30 EP disclosed
US-5521199-A TREATMENT OF ASTHMA ZENECA LIMITED (GB) 1996-05-28 US disclosed
EP-0625509-A1 N-alkyl substituted piperidine-derivatives with neurokinin receptor antagonist activity ZENECA LIMITED (GB) 1994-11-23 EP disclosed
CN-1017435-B PROCESS FOR PREPARATION OF GLYCEROL DERIVATIVES NIPPON CHEMIPHAR CO (JP) 1992-07-15 CN disclosed
CN-1030239-A The preparation method of new glycerol derivative NIPPON CHEMIPHAR CO (JP) 1989-01-11 CN 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 (3 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-20260099093-A1 PHOTOSENSITIVE RESIN COMPOSITION, METHOD FOR PRODUCING CURED RELIEF PATTERN USING SAME, AND METHOD FOR PRODUCING POLYIMIDE FILM USING SAME CD79B, ITGA1, PTK2 LMNA 3565/4885MEN1 2775/4885CYP2D6 4544/4885
US-20180208604-A1 FUSED RING PYRIMIDINE COMPOUND, INTERMEDIATE, AND PREPARATION METHOD, COMPOSITION AND USE THEREOF FLT3, FGFR1, FGFR3 LMNA 4690/4885MEN1 3448/4885CYP2D6 843/4885
US-10494378-B2 Fused ring pyrimidine compound, intermediate, and preparation method, composition and use thereof FLT3, FGFR1, FGFR3 LMNA 4690/4885MEN1 3448/4885CYP2D6 843/4885

“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.