SCHEMBL1979159

SCHEMBL1979159

COC(=O)CCC(=O)OC(C)C

nearest known ligand 0.65

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
TSHR P16473 7/20 0.65
LMNA P02545 4/20 0.54
KMT2A Q03164 2/20 0.48
MEN1 O00255 1/20 0.48
MAPT P10636 2/20 0.47
KDM4E B2RXH2 1/20 0.46
HTT P42858 2/20 0.45
HSD17B10 Q99714 2/20 0.45
ALDH1A1 P00352 1/20 0.45
CA12 O43570 2/20 0.41
CA14 Q9ULX7 2/20 0.41
CA7 P43166 1/20 0.41
CA9 Q16790 1/20 0.41
MGAM O43451 1/20 0.40
GAA P10253 1/20 0.40
SI P14410 1/20 0.40
MGAM2 Q2M2H8 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
SCHEMBL28298405 0.91 LMNA (0.67) TSHRLMNAKMT2AMEN1MAPT
SCHEMBL72471 0.89 LMNA (0.62) TSHRLMNAMAPTHTTALDH1A1
SCHEMBL13800475 0.89 LMNA (0.70) TSHRLMNAKMT2AMEN1MAPT
SCHEMBL31402602 0.87 LMNA (0.60) TSHRLMNAMAPTHTTALDH1A1
SCHEMBL2914094 0.83 TSHR (0.62) TSHRLMNAKMT2AMEN1MAPT
Dimethyl Succinate SCHEMBL28197342 0.82 TSHR (0.54) TSHRLMNAKMT2AMEN1MAPT
Dimethyl Succinate SCHEMBL28197354 0.82 TSHR (0.58) TSHRLMNAKMT2AMEN1MAPT
SCHEMBL1983440 0.82 MGAM (0.48) TSHRLMNAKMT2AMEN1MAPT
Butane SCHEMBL20558824 0.82 LMNA (0.68) TSHRLMNAMAPTHTTALDH1A1
SCHEMBL25182 0.82 LMNA (0.56) TSHRLMNAMAPTKDM4EHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118510877-A Cleaning composition for pretreatment of metal substrates, method for the production thereof and use thereof 巴斯夫涂料有限公司 2024-08-16 CN disclosed
WO-2023131530-A1 A CLEANING COMPOSITION FOR METAL SUBSTRATES PRETREATMENT AND ITS PREPARATION METHOD AND APPLICATION THEREOF BASF COATINGS GMBH (DE) 2023-07-13 WO disclosed
WO-2022138541-A1 POLYMETALLOXANE, COMPOSITION OF SAME, CURED FILM, METHOD FOR PRODUCING SAID CURED FILM, MEMBER AND ELECTRONIC COMPONENT EACH PROVIDED WITH SAID CURED FILM, FIBER, AND METHOD FOR PRODUCING SAID FIBER 東レ株式会社 2022-06-30 WO disclosed
US-9545104-B2 Liquid suspension concentrate formulations containing saflufenacil and glyphosate BASF SE (DE) 2017-01-17 US disclosed
CN-102655748-B Liquid suspension concentrate preparaton containing benzene flumetsulam BASF SE (DE) 2015-11-25 CN disclosed
CN-102651971-B Liquid suspension concentrate formulations containing saflufenacil and glyphosate BASF SE 2015-05-13 CN disclosed
US-8741809-B2 Liquid pyraclostrobin-containing crop protection formulations BASF SE (DE) 2014-06-03 US disclosed
US-8716182-B2 Liquid aqueous crop protection formulations BASF SE (DE) 2014-05-06 US disclosed
US-8703650-B2 Liquid suspension concentrate formulations containing saflufenacil BASF SE (DE) 2014-04-22 US disclosed
US-20120302444-A1 LIQUID SUSPENSION CONCENTRATE FORMULATIONS CONTAINING SAFLUFENACIL BASF SE (DE) 2012-11-29 US disclosed
EP-0218693-A1 CYCLOPENTADIENE DERIVATIVES AND THEIR METHOD OF PREPARATION ASHLAND OIL, INC. (US) 1987-04-22 EP disclosed
US-4636537-A CURABLE BINDER CONTAINING CYCLOPENTADIENE DERIVATIVES ASHLAND OIL, INC. (US) 1987-01-13 US disclosed
WO-1986006083-A1 CYCLOPENTADIENE DERIVATIVES, METHOD OF PREPARATION AND METHOD OF USE ASHLAND OIL, INC. (US) 1986-10-23 WO disclosed
US-4483961-A Polymeric cyclopentadiene derivatives, method for preparing and use thereof ASHLAND OIL, INC. (US) 1984-11-20 US disclosed
US-4482653-A Cyclopentadiene derivatives, method for preparing, and use thereof ASHLAND OIL, INC. (US) 1984-11-13 US disclosed
US-4464521-A EPOXIDIZED FULVENES AS BINDER FOR AGGREGATE; FOUNDRY BINDERS ASHLAND OIL, INC. (US) 1984-08-07 US disclosed
US-4412088-A CURABLE BINDER COMPOSITIONS ASHLAND OIL, INC. (US) 1983-10-25 US disclosed
US-4390675-A EPOXYFULVENE, ACID CATALYST ASHLAND OIL, INC. (US) 1983-06-28 US disclosed
US-4220578-A Method, resin and catalyst for increasing the tensile strength and core hardness of a sand mold or core CL INDUSTRIES INC. (US) 1980-09-02 US disclosed
US-4215012-A SULFUR-FREE; DIALKYL ESTER COMPOUND AND A LEWIS ACID, POLYMERIZATION CATALYST C L INDUSTRIES, INC. (US) 1980-07-29 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-20120302444-A1 LIQUID SUSPENSION CONCENTRATE FORMULATIONS CONTAINING SAFLUFENACIL SCD5, FFAR3, FFAR2 TSHR 2738/4885LMNA 402/4885KMT2A 305/4885

“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.