SCHEMBL681401

SCHEMBL681401

CNCc1cccc2ccccc12

nearest known ligand 0.66

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
IFNAR1 P17181 1/20 0.66
CA2 P00918 1/20 0.55
CYP1A2 P05177 2/20 0.53
CYP2C19 P33261 2/20 0.53
CYP2D6 P10635 1/20 0.53
CYP2C9 P11712 1/20 0.52
MC5R P33032 2/20 0.51
MAPK1 P28482 1/20 0.51
LMNA P02545 1/20 0.51
RECQL P46063 1/20 0.51
SMN1; SMN2 Q16637 1/20 0.51
MEN1 O00255 2/20 0.50
KMT2A Q03164 2/20 0.50
MC1R Q01726 1/20 0.50
HPGD P15428 1/20 0.50
MAPT P10636 1/20 0.49
MTNR1A P48039 1/20 0.49

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
SCHEMBL29434746 1.00 IFNAR1 (0.66) IFNAR1CA2CYP1A2CYP2C19CYP2D6
SCHEMBL5321295 1.00 IFNAR1 (0.66) IFNAR1CA2CYP1A2CYP2C19CYP2D6
Hydrochloric Acid SCHEMBL6251238 0.98 IFNAR1 (0.64) IFNAR1CA2CYP1A2CYP2C19CYP2D6
Hydrochloric Acid SCHEMBL1093699 0.98 IFNAR1 (0.64) IFNAR1CA2CYP1A2CYP2C19CYP2D6
SCHEMBL14110952 0.86 IFNAR1 (0.51) IFNAR1CA2CYP1A2CYP2C19CYP2D6
Isophthalic Acid SCHEMBL27488646 0.82 POLB (0.54) IFNAR1LMNARECQLSMN1; SMN2MEN1
SCHEMBL6008064 0.82 MC5R (0.70) CA2CYP1A2CYP2C19CYP2D6CYP2C9
SCHEMBL3144929 0.82 IFNAR1 (0.51) IFNAR1CA2MC5RMAPK1LMNA
SCHEMBL19144969 0.80 CA2 (0.56) CA2CYP1A2CYP2C19CYP2D6CYP2C9
SCHEMBL30996076 0.80 IFNAR1 (1.00) IFNAR1CYP1A2CYP2C19CYP2D6CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120117949-A Method for directly preparing tertiary amine compound from aromatic aldehyde, ketone and secondary amine 湖南大学 2025-06-10 CN claimed
CN-115073303-B Preparation method of terbinafine hydrochloride Z-type isomer 乐泰药业(兰西)有限公司 2025-02-14 CN claimed
CN-113493388-B Synthesis method of butenafine hydrochloride 鲁南制药集团股份有限公司 2024-05-10 CN claimed
CN-113979871-B Preparation method of N-methyl-1-naphthylmethylamine and intermediate N-methyl-1-naphthylmethylamine 江苏同禾药业有限公司 2023-11-10 CN claimed
CN-112209838-B Preparation method of butenaphthol hydrochloride 鲁南制药集团股份有限公司 2023-02-17 CN claimed
CN-114380696-B Preparation method of terbinafine hydrochloride 山东诚汇双达药业有限公司 2022-11-25 CN claimed
CN-112552182-B New synthesis process of naftifine drug intermediate N-methyl-1-naphthylmethylamine 杭州新桂实业有限公司 2022-10-11 CN claimed
CN-115073303-A Preparation method of terbinafine hydrochloride Z-type isomer 乐泰药业(兰西)有限公司 2022-09-20 CN claimed
CN-114380696-A Preparation method of terbinafine hydrochloride 山东诚汇双达药业有限公司 2022-04-22 CN claimed
CN-110423200-B Method for improving purity of terbinafine hydrochloride 成都奥邦药业有限公司 2022-03-25 CN claimed
EP-1458668-A1 PROCESS FOR PREPARING TERBINAFINE AND HCI SALT THEREOF YUHAN CORPORATION, LTD. (KR) 2004-09-22 EP claimed
US-6689913-B2 REDUCTIVE ALKYLATION OF THE REACTION PRODUCT OF AN S-SUBSTITUTED-C-TERT-BUTYL-N-SULFONYLHYDRAZONYLFURAN AND A BASE WITH N-METHYL-1-NAPHTHALENEMETHYLAMINE OR ITS HCL SALT YUHAN CORPORATION (KR) 2004-02-10 US claimed
US-20030130530-A1 Process for preparing terbinafine and HCI salt thereof YUHAN CORPORATION (KR) 2003-07-10 US claimed
WO-2003055844-A1 PROCESS FOR PREPARING TERBINAFINE AND HCI SALT THEREOF YUHAN CORPORATION (KR) 2003-07-10 WO claimed
EP-1143950-A3 TOPICAL APPLICATION PRODUCTS IPR-Institute for Pharmaceutical Research AG (CH) 2002-05-15 EP claimed
WO-2001077064-A1 METHOD FOR THE PREPARATION OF (E)-N-(6,6-DIMETHYL-2-HEPTEN-4-YNYL)-N-METHYL-1-NAPHTHALENEMETHANAMINE (TERBINAFINE) SLOVAKOFARMA A.S. (SK) 2001-10-18 WO claimed
EP-1143950-A2 TOPICAL APPLICATION PRODUCTS IPR-Institute for Pharmaceutical Research AG (CH) 2001-10-17 EP claimed
WO-2000015202-A2 TOPICAL APPLICATION PRODUCTS IPR-INSTITUTE FOR PHARMACEUTICAL RESEARCH AG (CH) 2000-03-23 WO claimed
US-5817875-A Methods for the manufacture of terbinafine KARIMIAN KHASHAYAR (CA) 1998-10-06 US claimed
EP-0363326-A2 Fungicidal amines SANDOZ AG (CH) 1990-04-11 EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 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-20030130530-A1 Process for preparing terbinafine and HCI salt thereof TPMT, HNMT, BHMT IFNAR1 1122/4885CA2 3960/4885CYP1A2 291/4885

“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.