SCHEMBL5491789

SCHEMBL5491789

CCCCNC(=O)C(CC)CCCC

nearest known ligand 0.71

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
USP2 O75604 2/20 0.71
CA2 P00918 6/20 0.66
CA1 P00915 4/20 0.66
TSHR P16473 2/20 0.59
MAPK1 P28482 2/20 0.55
DPP7 Q9UHL4 2/20 0.55
MMP2 P08253 1/20 0.47
MEN1 O00255 1/20 0.46
ALDH1A1 P00352 1/20 0.46
MAPT P10636 1/20 0.46
KMT2A Q03164 1/20 0.46
SMN1; SMN2 Q16637 1/20 0.46
RRM1 P23921 1/20 0.46
EPHX1 P07099 2/20 0.45

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
SCHEMBL11692574 0.98 USP2 (0.69) USP2CA2CA1TSHRMAPK1
SCHEMBL22414705 0.94 USP2 (0.69) USP2CA2CA1TSHRMAPK1
SCHEMBL23140154 0.92 USP2 (0.61) USP2CA2CA1TSHRMAPK1
SCHEMBL18541163 0.92 USP2 (0.66) USP2CA2CA1TSHRMAPK1
SCHEMBL16390491 0.91 USP2 (0.65) USP2CA2CA1TSHRMAPK1
SCHEMBL13296411 0.90 USP2 (0.74) USP2CA2CA1TSHRDPP7
SCHEMBL16342174 0.89 USP2 (0.62) USP2CA2CA1TSHRMAPK1
SCHEMBL18664494 0.89 USP2 (0.62) USP2CA2CA1TSHRMAPK1
SCHEMBL3117146 0.87 USP2 (0.60) USP2CA2CA1TSHRMAPK1
SCHEMBL17624932 0.86 USP2 (0.59) USP2CA2CA1TSHRDPP7

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 11 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107619950-B Extraction composition, extraction system and application thereof 中国科学院上海有机化学研究所 2021-04-20 CN claimed
CN-111749022-A Low-foam high-concentration scouring agent and preparation method thereof 淄博鲁瑞精细化工有限公司 2020-10-09 CN claimed
CN-107851470-B Method for treating aqueous nitric acid solution resulting from dissolution of spent nuclear fuel 原子能和替代能源委员会 2020-07-28 CN claimed
CN-110312702-B Asymmetric N, N-dialkylamides, in particular for separating uranium (VI) and plutonium (IV), their synthesis and use 原子能和替代能源委员会 2022-10-14 CN disclosed
CN-111749022-A Low-foam high-concentration scouring agent and preparation method thereof 淄博鲁瑞精细化工有限公司 2020-10-09 CN disclosed
CN-107851470-B Method for treating aqueous nitric acid solution resulting from dissolution of spent nuclear fuel 原子能和替代能源委员会 2020-07-28 CN disclosed
CN-107922314-B Novel asymmetric N, N-dialkyl amide and synthetic method and application thereof 欧安诺循环 2020-07-07 CN disclosed
US-7199101-B2 Gelling agent for oil AJINOMOTO CO., INC. (JP) 2007-04-03 US disclosed
US-20050100572-A1 Gelling agent for oil AJINOMOTO CO., INC. (JP) 2005-05-12 US disclosed
US-4011180-A NOVEL COCATALYST SYSTEM FOR TRIMERIZING POLYISOCYANATES THE UPJOHN COMPANY (US) 1977-03-08 US disclosed
US-4003859-A CATALYST OF AN AMINE, AMIDE SALT AND DIBUTYL TIN(ALKANOATE) THE UPJOHN COMPANY (US) 1977-01-18 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 (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-20050100572-A1 Gelling agent for oil FASN, NR1H3, CCNB2 USP2 2558/4885CA2 4627/4885CA1 4374/4885

“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.