SCHEMBL307790

SCHEMBL307790

Cc1cccc(C)c1NC(=O)CCl

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 3/20 0.62
KMT2A Q03164 3/20 0.62
CYP1A2 P05177 2/20 0.62
CYP2C9 P11712 2/20 0.62
NFKB1 P19838 1/20 0.62
CYP2C19 P33261 1/20 0.62
SMN1; SMN2 Q16637 4/20 0.61
ALDH1A1 P00352 9/20 0.59
LMNA P02545 7/20 0.59
MAPT P10636 3/20 0.59
SCN3A Q9NY46 3/20 0.59
SCN1A P35498 2/20 0.59
SCN2A Q99250 2/20 0.59
HDAC3 O15379 1/20 0.59
HDAC4 P56524 1/20 0.59
HDAC1 Q13547 1/20 0.59
HDAC7 Q8WUI4 1/20 0.59
HDAC2 Q92769 1/20 0.59
HDAC10 Q969S8 1/20 0.59
HDAC11 Q96DB2 1/20 0.59

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
SCHEMBL6570220 0.93 KMT2A (0.56) MEN1KMT2ACYP1A2CYP2C9NFKB1
SCHEMBL25224075 0.91 MEN1 (0.54) MEN1KMT2ACYP1A2CYP2C9NFKB1
SCHEMBL4901648 0.89 SMN1; SMN2 (0.54) MEN1KMT2ACYP1A2CYP2C9NFKB1
SCHEMBL5528418 0.89 ALDH1A1 (0.66) MEN1KMT2ACYP1A2CYP2C9NFKB1
SCHEMBL18297043 0.88 ALDH1A1 (0.58) MEN1KMT2ACYP1A2CYP2C9NFKB1
SCHEMBL18296970 0.88 SMN1; SMN2 (0.53) MEN1KMT2ACYP1A2CYP2C9NFKB1
SCHEMBL6546027 0.88 POLB (0.61) MEN1KMT2ACYP1A2CYP2C9SMN1; SMN2
SCHEMBL30323772 0.88 POLB (0.61) MEN1KMT2ACYP1A2CYP2C9SMN1; SMN2
SCHEMBL6259358 0.87 ALDH1A1 (0.51) MEN1KMT2ACYP1A2CYP2C9NFKB1
SCHEMBL11040582 0.86 SMN1; SMN2 (0.51) MEN1KMT2ACYP1A2CYP2C9NFKB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114644571-B Lidocaine impurity, application thereof in detection method and detection method 威智医药股份有限公司 2024-07-23 CN claimed
CN-118255724-A Synthesis method of lidocaine hydrochloride impurity and reaction detection method thereof 河北天成药业股份有限公司 2024-06-28 CN claimed
CN-118130654-A Compound lidocaine prednisolone gel related substance and BHT content analysis method 中国牧工商集团有限公司 2024-06-04 CN claimed
CN-117665142-A Method for detecting impurities in cardioplegic solution 成都青山利康药业股份有限公司 2024-03-08 CN claimed
CN-112557569-B Method for detecting related substances in lidocaine 南京海纳医药科技股份有限公司 2023-04-11 CN claimed
CN-115322112-A Preparation method of 2-chloro-N- (2,6-xylyl) acetamide 山东创新药物研发有限公司 2022-11-11 CN claimed
CN-114644571-A Lidocaine impurity, application of lidocaine impurity in detection method and detection method 威智医药有限公司 2022-06-21 CN claimed
CN-114315632-A Preparation method of ranolazine intermediate impurity 海南鑫开源医药科技有限公司 2022-04-12 CN claimed
WO-2021159754-A1 METHOD FOR PREPARING LIDOCAINE INTERMEDIATE α-CHLOROACETYL-2,6-DIMETHYLANILINE AND LIDOCAINE WITHOUT ADDING ADDITIONAL ALKALI 郑州原理生物科技有限公司 2021-08-19 WO claimed
CN-111253273-A Method for preparing lidocaine intermediate α -chloroacetyl-2, 6-dimethylaniline and lidocaine without adding extra alkali 郑州原理生物科技有限公司 2020-06-09 CN claimed
CN-100494187-C Method for synthesizing Ranolazine JIE YAN (CN) 2009-06-03 CN claimed
EP-1517900-B1 PROCESS FOR THE PRODUCTION OF N-(2,6-DIMETHYL-PHENYL)-2-PIPERAZIN-1-YL-ACETAMIDE JANSSEN PHARMACEUTICA NV (BE) 2009-05-27 EP claimed
WO-2008047388-A2 IMPROVED PROCESS FOR THE PREPARATION OF RANOLAZINE IND-SWIFT LABORATORIES LIMITED (IN) 2008-04-24 WO claimed
CN-1915982-A Method for synthesizing Ranolazine YAN JIE (CN) 2007-02-21 CN claimed
US-20050240018-A1 Process for the production of n-(2,6-dimethyl-phenyl)-2-piperazin-1-yl-acetamide JANSSEN PHARMACEUTICA, N.V. (BE) 2005-10-27 US claimed
EP-1517900-A1 PROCESS FOR THE PRODUCTION OF N-(2,6-DIMETHYL-PHENYL)-2-PIPERAZIN-1-YL-ACETAMIDE JANSSEN PHARMACEUTICA N.V. (BE) 2005-03-30 EP claimed
WO-2004000824-A1 PROCESS FOR THE PRODUCTION OF N-(2,6-DIMETHYL-PHENYL)-2-PIPERAZIN-1-YL-ACETAMIDE JANSSEN PHARMACEUTICA N.V. (BE) 2003-12-31 WO claimed
EP-0839800-B1 Process for preparing halogenoacetamide derivatives DAIICHI SEIYAKU CO (JP) 2002-10-23 EP claimed
US-5461157-A Process for preparing pyrrolidinylacetamide derivatives DAIICHI PHARMACEUTICAL CO., LTD. (JP) 1995-10-24 US claimed
US-4248678-A Alkylating of nitrogen acids using electrogenerated bases as catalysts MONSANTO COMPANY (US) 1981-02-03 US 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-20050240018-A1 Process for the production of n-(2,6-dimethyl-phenyl)-2-piperazin-1-yl-acetamide SCN5A, SCN2A, NAA15 MEN1 4527/4885KMT2A 331/4885CYP1A2 1583/4885

“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.