SCHEMBL28883

SCHEMBL28883

CC(C)(C)C(=O)Nc1ccc(Cl)cc1

nearest known ligand 0.79

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 1/20 0.79
PDK1 Q15118 1/20 0.66
PDK2 Q15119 1/20 0.66
PDK3 Q15120 1/20 0.66
PDK4 Q16654 1/20 0.66
MEN1 O00255 2/20 0.64
KMT2A Q03164 2/20 0.64
TDP1 Q9NUW8 1/20 0.64
MAPT P10636 5/20 0.61
ALDH1A1 P00352 2/20 0.61
CA12 O43570 1/20 0.58
CA1 P00915 1/20 0.58
CA2 P00918 1/20 0.58
CA7 P43166 1/20 0.58
CA9 Q16790 1/20 0.58
CA14 Q9ULX7 1/20 0.58
NPC1 O15118 5/20 0.56
RAB9A P51151 4/20 0.56
SMN1; SMN2 Q16637 3/20 0.56
TSHR P16473 1/20 0.55

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
SCHEMBL383652 0.94 L3MBTL1 (0.70) L3MBTL1PDK1PDK2PDK3PDK4
SCHEMBL7733701 0.89 L3MBTL1 (1.00) L3MBTL1MEN1KMT2AMAPTALDH1A1
SCHEMBL11537675 0.86 PDK1 (0.59) L3MBTL1PDK1PDK2PDK3PDK4
SCHEMBL19853109 0.84 PDK1 (0.62) L3MBTL1PDK1PDK2PDK3PDK4
Hydrochloric Acid SCHEMBL19841199 0.82 PDK1 (0.60) L3MBTL1PDK1PDK2PDK3PDK4
SCHEMBL11249289 0.82 PDK1 (0.60) L3MBTL1PDK1PDK2PDK3PDK4
SCHEMBL7424794 0.82 PDK1 (0.60) L3MBTL1PDK1PDK2PDK3PDK4
SCHEMBL13171374 0.82 RHOC (0.64) L3MBTL1MEN1KMT2AMAPTNPC1
SCHEMBL10386145 0.81 PDK1 (0.58) L3MBTL1PDK1PDK2PDK3PDK4
SCHEMBL1422823 0.81 L3MBTL1 (0.83) L3MBTL1MEN1KMT2AMAPTALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119954705-A Indole derivative and preparation method thereof 南阳师范学院 2025-05-09 CN claimed
CN-116808967-A 4-chloro-2-trifluoroacetyl aniline hydrochloride micro-channel reactor and synthesis method 江西华洲科技有限公司 2023-09-29 CN claimed
CN-108947855-B Synthesis method of efavirenz key intermediate 江苏沙星化工有限公司 2021-10-22 CN claimed
CN-108947855-A A kind of synthetic method of efavirenz key intermediate 江苏沙星化工有限公司 2018-12-07 CN claimed
US-20250197360-A1 NOVEL DIAZEPINES THAT TARGET YELLOW FEVER VIRUS NON-STRUCTURAL 4B (NS4B) PROTEIN AND THEIR METHOD OF USE BARUCH S. BLUMBERG INSTITUTE 2025-06-19 US disclosed
CN-119954705-A Indole derivative and preparation method thereof 南阳师范学院 2025-05-09 CN disclosed
CN-222641616-U Processing apparatus of lithium chloride crystallization is precipitated in waste liquid 黄石市博尔化工有限公司 2025-03-21 CN disclosed
CN-119072467-A Novel diazapine compounds targeting yellow fever virus non-structural 4B (NS 4B) protein and methods of use thereof 巴鲁克斯布伦博格研究所 2024-12-03 CN disclosed
CN-220182843-U Waste liquid treatment device 江西华洲科技有限公司 2023-12-15 CN disclosed
CN-116808967-A 4-chloro-2-trifluoroacetyl aniline hydrochloride micro-channel reactor and synthesis method 江西华洲科技有限公司 2023-09-29 CN disclosed
WO-2023172726-A1 NOVEL DIAZEPINES THAT TARGET YELLOW FEVER VIRUS NON-STRUCTURAL 4B (NS4B) PROTEIN AND THEIR METHOD OF USE BARUCH S. BLUMBERG INSTITUTE (US) 2023-09-14 WO disclosed
WO-2023172726-A1 NOVEL DIAZEPINES THAT TARGET YELLOW FEVER VIRUS NON-STRUCTURAL 4B (NS4B) PROTEIN AND THEIR METHOD OF USE BARUCH S. BLUMBERG INSTITUTE (US) 2023-09-14 WO disclosed
EP-0663899-A4 SUBSTITUTED KYNURENINES, A PROCESS FOR THEIR PREPARATION, AND USE AS MEDICAMENTS. UNIV MARYLAND (US) 1996-01-17 EP disclosed
WO-1995020389-A1 BENZOXAZINONES AS INHIBITORS OF HIV REVERSE TRANSCRIPTASE MERCK & CO., INC. (US) 1995-08-03 WO disclosed
EP-0663899-A1 SUBSTITUTED KYNURENINES, A PROCESS FOR THEIR PREPARATION, AND USE AS MEDICAMENTS THE UNIVERSITY OF MARYLAND AT BALTIMORE (US) 1995-07-26 EP disclosed
WO-1995004714-A1 SUBSTITUTED KYNURENINES, A PROCESS FOR THEIR PREPARATION, AND USE AS MEDICAMENTS UNIVERSITY OF MARYLAND AT BALTIMORE (US) 1995-02-16 WO disclosed
WO-1994003440-A1 BENZOXAZINONES AS INHIBITORS OF HIV REVERSE TRANSCRIPTASE MERCK & CO., INC. (US) 1994-02-17 WO disclosed
EP-0582455-A1 Benzoxazinones as inhibitors of HIV reverse transcriptase MERCK & CO. INC. (US) 1994-02-09 EP disclosed
EP-0070171-B1 NOVEL PIPERIDINE DERIVATIVES, PROCESSES FOR PREPARATION THEREOF AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME KYOWA HAKKO KOGYO CO., LTD (JP) 1986-10-15 EP disclosed
EP-0070171-A1 Novel piperidine derivatives, processes for preparation thereof and pharmaceutical compositions containing same KYOWA HAKKO KOGYO CO., LTD (JP) 1983-01-19 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 (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-20250197360-A1 NOVEL DIAZEPINES THAT TARGET YELLOW FEVER VIRUS NON-STRUCTURAL 4B (NS4B) PROTEIN AND THEIR METHOD OF USE CUL4B, BRD4, CUL4A L3MBTL1 3709/4885PDK1 3874/4885PDK2 1600/4885

“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.