SCHEMBL531889

SCHEMBL531889

c1ccc2[nH]c(C3CCNCC3)nc2c1

nearest known ligand 0.73

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
PARP1 P09874 2/20 0.52
HTR2B P41595 4/20 0.52
NPY5R Q15761 1/20 0.51
KMT2A Q03164 2/20 0.50
PKM P14618 1/20 0.49
HTR3A P46098 1/20 0.49
ALDH1A1 P00352 1/20 0.49
POLB P06746 1/20 0.49
MAPT P10636 1/20 0.49
HPGD P15428 1/20 0.49
TSHR P16473 1/20 0.49
MEN1 O00255 1/20 0.47

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 SCHEMBL1299145 0.98 HTR2B (0.51) PARP1HTR2BNPY5RKMT2APKM
SCHEMBL1299363 0.90 PARP1 (0.54) PARP1HTR2BNPY5RKMT2APKM
Carbamic Acid SCHEMBL28440834 0.90 PARP1 (0.61) PARP1HTR2B
SCHEMBL2276872 0.89 ALDH1A1 (0.59) HTR2BNPY5RKMT2APKMALDH1A1
Hydrochloric Acid SCHEMBL31596380 0.87 MAPT (0.57) HTR2BNPY5RKMT2APKMALDH1A1
SCHEMBL2674802 0.86 HTR2B (0.55) HTR2BNPY5RKMT2APOLBMAPT
SCHEMBL6756134 0.86 NPC1 (0.59) HTR2BNPY5RKMT2APOLBMAPT
SCHEMBL6757201 0.84 NPC1 (0.62) HTR2BNPY5RPOLBMAPT
SCHEMBL724921 0.84 NPC1 (0.62) HTR2BNPY5RPOLBMAPT
SCHEMBL2491336 0.83 HTR2B (0.52) HTR2BNPY5RKMT2APKMALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117924240-A Synthesis process of 4- (1H-benzo [ D ] imidazole-2-yl) piperidine-1-carboxylic acid tert-butyl ester 江苏恒沛药物科技有限公司 2024-04-26 CN claimed
CN-109694367-B Method for preparing bilastine 湖北省医药工业研究院有限公司 2021-06-11 CN claimed
CN-112110893-A Preparation method of bilastine 山东齐环医药科技有限公司 2020-12-22 CN claimed
CN-109206455-A It is used to prepare the aryl ruthenium complex and its preparation method and application for the treatment of liver-cancer medicine 广西中医药大学 2019-01-15 CN claimed
CN-109180741-A Ruthenium (II) complex and its preparation method and application for treating gastric cancer 广西中医药大学 2019-01-11 CN claimed
CN-108752390-A With phototoxic antitumoral compounds and its preparation method and application 广西中医药大学 2018-11-06 CN claimed
CN-107857702-A A kind of preparation method of bilastine intermediate 重庆华邦制药有限公司 2018-03-30 CN claimed
US-12503458-B2 5-hydroxytryptamine receptor 7 activity modulators and their method of use TEMPLE UNIVERSITY OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2025-12-23 US disclosed
US-20250273719-A1 ION-EXCHANGE MEMBRANE, MEMBRANE ELECTRODE ASSEMBLY, CELL FOR REDOX FLOW BATTERY, AND REDOX FLOW BATTERY ASAHI KASEI KABUSHIKI KAISHA (JP) 2025-08-28 US disclosed
EP-4463452-B1 C-MYC MRNA TRANSLATION MODULATORS AND USES THEREOF IN THE TREATMENT OF CANCER ANIMA BIOTECH INC (US) 2025-07-30 EP disclosed
US-12344600-B2 c-Myc mRNA translation modulators and uses thereof in the treatment of cancer ANIMA BIOTECH INC. (US) 2025-07-01 US disclosed
WO-2025129167-A1 INHIBITORS OF THE SURFACE EXPRESSION OF THE VOLTAGE-GATED SODIUM ION CHANNEL 1.7 (NAV1.7) AND THEIR THERAPEUTIC USES THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPT. OF HEALTH AND HUMAN SERVICES (US) 2025-06-19 WO disclosed
CN-114591292-B Bilastine intermediate compounds 鲁南制药集团股份有限公司 2025-06-17 CN disclosed
EP-1181287-A1 SULFONAMIDE COMPOUNDS WITH PHARMACEUTICAL ACTIVITY SMITHKLINE BEECHAM PLC (GB) 2002-02-27 EP disclosed
WO-2002014315-A2 SUBSTITUTED PYRAZOLES ORTHO MCNEIL PHARMACEUTICAL, INC. (US) 2002-02-21 WO disclosed
WO-2001029029-A1 TETRAHYDROBENZINDOLONE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS 5-HT7 RECEPTOR ANTAGONISTS SMITHKLINE BEECHAM P.L.C. (GB) 2001-04-26 WO disclosed
WO-2000073299-A1 SULFONAMIDE COMPOUNDS WITH PHARMACEUTICAL ACTIVITY SMITHKLINE BEECHAM P.L.C. (GB) 2000-12-07 WO disclosed
WO-2000037074-A1 MUTILIN 14-ESTER DERIVATIVES HAVING ANTIBACTERIAL ACTIVITY SMITHKLINE BEECHAM PLC (GB) 2000-06-29 WO disclosed
US-5877187-A Benzimidazole derivatives with antihistaminic activity FABRICA ESPANOLA DE PRODUCTOS QUIMICOS Y FARMACEUTICOS S.A. (FAES) (ES) 1999-03-02 US disclosed
EP-0818454-A1 Benzimidazole derivatives with antihistaminic activity FABRICA ESPANOLA DE PRODUCTOS QUIMICOS Y FARMACEUTICOS, S.A. (FAES) (ES) 1998-01-14 EP 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 (2 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-12503458-B2 5-hydroxytryptamine receptor 7 activity modulators and their method of use HTR7, HTR5A, HTR6 PARP1 2479/4885HTR2B 11/4885NPY5R 21/4885
US-12344600-B2 c-Myc mRNA translation modulators and uses thereof in the treatment of cancer MYC, MYCBP, MYCBP2 PARP1 1831/4885HTR2B 4574/4885NPY5R 4628/4885

“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.