SCHEMBL5543216

SCHEMBL5543216

Cc1ccc(NC=O)cc1C

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 6/20 0.49
SMN1; SMN2 Q16637 5/20 0.49
RAB9A P51151 5/20 0.49
NPC1 O15118 4/20 0.49
LMNA P02545 2/20 0.49
POLB P06746 2/20 0.48
ALDH1A1 P00352 6/20 0.44
HTT P42858 2/20 0.44
NFKB1 P19838 2/20 0.44
NFKB2 Q00653 2/20 0.44
RELA Q04206 2/20 0.44
KMT2A Q03164 2/20 0.41
MEN1 O00255 1/20 0.41
TP53 P04637 1/20 0.41
GAA P10253 1/20 0.41
HDAC3 O15379 1/20 0.40
HDAC4 P56524 1/20 0.40
HDAC1 Q13547 1/20 0.40
HDAC7 Q8WUI4 1/20 0.40
HDAC2 Q92769 1/20 0.40

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
SCHEMBL30555452 1.00 MAPT (0.49) MAPTSMN1; SMN2RAB9ANPC1LMNA
SCHEMBL22472061 0.84 KDM4E (0.43) MAPTSMN1; SMN2RAB9ANPC1LMNA
SCHEMBL10952795 0.83 ALDH1A1 (0.41) MAPTSMN1; SMN2RAB9ANPC1LMNA
SCHEMBL29375021 0.83 ALDH1A1 (0.41) MAPTSMN1; SMN2RAB9ANPC1LMNA
SCHEMBL9597648 0.83 ALDH1A1 (0.41) MAPTSMN1; SMN2RAB9ANPC1LMNA
SCHEMBL19444177 0.81 SMN1; SMN2 (0.48) MAPTSMN1; SMN2RAB9ANPC1LMNA
SCHEMBL20635358 0.81 RAB9A (0.53) MAPTRAB9ANPC1LMNAPOLB
SCHEMBL22053915 0.81 ALDH1A1 (0.40) MAPTSMN1; SMN2RAB9ANPC1LMNA
SCHEMBL2324287 0.81 KMT2A (0.46) MAPTSMN1; SMN2RAB9ANPC1LMNA
SCHEMBL5462851 0.81 TP53 (0.45) MAPTSMN1; SMN2RAB9ANPC1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112898206-A Preparation method of 5, 6-dimethylbenzimidazole 河北凡博医药科技有限公司 2021-06-04 CN claimed
EP-1189891-A1 TRIAZOLE COMPOUNDS AND COMBINATORIAL LIBRARIES THEREOF LION Bioscience AG (DE) 2002-03-27 EP claimed
US-6362342-B1 BIOSYNTHESIS; DRUG LIBRARIES LION BIOSCIENCE AG (DE) 2002-03-26 US claimed
WO-2001000594-A1 TRIAZOLE COMPOUNDS AND COMBINATORIAL LIBRARIES THEREOF LION BIOSCIENCE AG (DE) 2001-01-04 WO claimed
US-4861872-A Alkyl-phenylcarbamate derivative of polysaccharide DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1989-08-29 US claimed
EP-0281951-A1 Alkyl-phenylcarbamate derivative of polysaccharide DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1988-09-14 EP claimed
EP-3915994-B9 COMPOUNDS AND COMPOSITIONS FOR INDUCING CHONDROGENESIS NOVARTIS AG (CH) 2024-02-28 EP disclosed
CN-116655638-B Deuterated PRMT5 inhibitors 上海齐鲁制药研究中心有限公司 2024-01-26 CN disclosed
CN-116655638-A Deuterated PRMT5 inhibitors 上海齐鲁制药研究中心有限公司 2023-08-29 CN disclosed
CN-112898206-A Preparation method of 5, 6-dimethylbenzimidazole 河北凡博医药科技有限公司 2021-06-04 CN disclosed
CN-112898206-A Preparation method of 5, 6-dimethylbenzimidazole 河北凡博医药科技有限公司 2021-06-04 CN disclosed
US-10195213-B2 Chemical entities that kill senescent cells for use in treating age-related disease UNITY BIOTECHNOLOGY, INC. (US) 2019-02-05 US disclosed
US-20170281649-A1 COMPOUNDS AND THERAPEUTIC USES UNITY BIOTECHNOLOGY, INC. 2017-10-05 US disclosed
US-4391953-A Diene rubber compositions containing N,N'-dithioformanilide crosslinkers MONSANTO COMPANY (US) 1983-07-05 US disclosed
US-4228103-A Effecting condensation of nitrohaloarene and formyl derivative of a primary aromatic amine with alkali metal hydroxide MONSANTO COMPANY (US) 1980-10-14 US disclosed
US-4209463-A Promoting the formation of nitrodiarylamines from nitrohaloarenes, activated aryl amines and sodium carbonates MONSANTO COMPANY (US) 1980-06-24 US disclosed
US-4196146-A Making nitrodiarylamines from formyl derivatives of aromatic amines and nitrohaloarenes by admixing with certain aqueous salt solutions MONSANTO COMPANY (US) 1980-04-01 US disclosed
US-4187248-A FORMANILIDE MONSANTO COMPANY (US) 1980-02-05 US disclosed
US-4187249-A COMPOUNDS OF POTASSIUM, CESIUM, OR RUBIDIUM MONSANTO COMPANY (US) 1980-02-05 US disclosed
US-4140716-A Process for making an amide of formic acid and forming nitrodiarylamine therefrom MONSANTO COMPANY (US) 1979-02-20 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 (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-20170281649-A1 COMPOUNDS AND THERAPEUTIC USES TP53, NQO1, SHMT2 MAPT 1762/4885SMN1; SMN2 595/4885RAB9A 1412/4885
US-10195213-B2 Chemical entities that kill senescent cells for use in treating age-related disease TP53, CDKN1A, GLA MAPT 1460/4885SMN1; SMN2 839/4885RAB9A 831/4885

“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.