SCHEMBL2692874

SCHEMBL2692874

CC1(C)[C@@H](C=O)[C@@H]1C(=O)O

nearest known ligand 0.33

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.33
APLNR P35414 1/20 0.32
UGT2B7 P16662 1/20 0.31
KMT2A Q03164 1/20 0.31

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
SCHEMBL515780 1.00 LMNA (0.33) LMNAAPLNRUGT2B7KMT2A
SCHEMBL8037708 1.00 LMNA (0.33) LMNAAPLNRUGT2B7KMT2A
SCHEMBL3247829 1.00 LMNA (0.33) LMNAAPLNRUGT2B7KMT2A
SCHEMBL3216533 1.00 LMNA (0.33) LMNAAPLNRUGT2B7KMT2A
SCHEMBL358648 1.00 LMNA (0.33) LMNAAPLNRUGT2B7KMT2A
SCHEMBL11136789 0.80 LMNA (0.37) LMNA
SCHEMBL7064292 0.80 LMNA (0.37) LMNA
SCHEMBL3678270 0.79 UGT2B7 (0.32) LMNAUGT2B7
SCHEMBL3658221 0.79 UGT2B7 (0.32) LMNAUGT2B7
SCHEMBL11055234 0.79 UGT2B7 (0.32) LMNAUGT2B7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0132168-B1 ESTERS OF CYCLOPROPANECARBOXYLIC ACIDS BEARING A CYANO GROUP, PREPARATION PROCESS AND INTERMEDIATES, THEIR USE AS PESTICIDES AND COMPOSITIONS CONTAINING THEM ROUSSEL-UCLAF (FR) 1987-06-16 EP claimed
EP-1970369-B1 METHOD FOR PRODUCING PURIFIED FORMYLCYCLOPROPANE COMPOUND AND INTERMEDIATE OF SUCH FORMYLCYCLOPROPANE COMPOUND SUMITOMO CHEMICAL CO (JP) 2013-09-25 EP disclosed
US-8168816-B2 Method for producing purified formylcyclopropane compound and intermediate of such formylcyclopropane compound SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2012-05-01 US disclosed
US-20100305353-A1 METHOD FOR PRODUCING PURIFIED FORMYLCYCLOPROPANE COMPOUND AND INTERMEDIATE OF SUCH FORMYLCYCLOPROPANE COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2010-12-02 US disclosed
CN-101506142-A Process for production of trans-2,2-dimethyl- 3-formylcyclopropane carboxylic acid ester SUMITOMO CHEMICAL CO (JP) 2009-08-12 CN disclosed
EP-2053037-A1 PROCESS FOR PRODUCTION OF TRANS-2,2-DIMETHYL- 3-FORMYLCYCLOPROPANE CARBOXYLIC ACID ESTER Sumitomo Chemical Company, Limited (JP) 2009-04-29 EP disclosed
EP-1970369-A1 METHOD FOR PRODUCING PURIFIED FORMYLCYCLOPROPANE COMPOUND AND INTERMEDIATE OF SUCH FORMYLCYCLOPROPANE COMPOUND Sumitomo Chemical Company, Limited (JP) 2008-09-17 EP disclosed
EP-1463706-B1 PROCESS FOR PRODUCTION OF 3,3-DIMETHYL-2-FORMYLCYCLOPROPANECARBOXYLIC ACID DERIVATIVES SUMITOMO CHEMICAL CO (JP) 2008-02-27 EP disclosed
US-7262320-B2 Process for production of 3,3-dimethyl-2-formylcyclopropanecarboxylic acid derivatives SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2007-08-28 US disclosed
US-20050090685-A1 Process for production of 3,3-dimethyl-2-formylcyclopropanecarboxylic acid derivatives SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2005-04-28 US disclosed
US-4996349-A Reducing dioxolane diester to dialdehyde, adding ester using organic phosphorus compound, reacting with gem-dimethylcyclo-propanation reagent, hydrolyzing, cleaving ROUSSEL UCLAF (FR) 1991-02-26 US disclosed
EP-0305289-A1 Enantioselective process for preparing derivatives of trans- or cis-hemicaronaldehyde, and intermediates obtained ROUSSEL-UCLAF (FR) 1989-03-01 EP disclosed
EP-0162538-A2 Cyclopropane derivates IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1985-11-27 EP disclosed
US-4482731-A Process for the preparation of trans-3-(z-2-chloro-2-aryl-vinyl)-2,2-dimethyl-cyclopropane-1-carboxylic acid derivatives, and the use of intermediate products in agents for compating pests BAYER AKTIENGESELLSCHAFT (DE) 1984-11-13 US disclosed
US-4440947-A Preparation of substituted alpha-halogeno-propionic acids and their derivatives BAYER AKTIENGESELLSCHAFT (DE) 1984-04-03 US disclosed
US-4435597-A Preparation of caronaldehyde acid and derivatives thereof BAYER AKTIENGESELLSCHAFT (DE) 1984-03-06 US disclosed
US-4206140-A INSECTICIDES, ANTHELMINTICS ROUSSEL UCLAF (FR) 1980-06-03 US disclosed
US-4101574-A Cyclopropanecarboxylic acid chlorides ROUSSEL UCLAF (FR) 1978-07-18 US disclosed
US-4014918-A Process for the preparation of cyclopropane derivatives and compounds produced therein ROUSSEL-UCLAF (FR) 1977-03-29 US disclosed
US-3997586-A Cyclopropanecarboxylic acids and esters ROUSSEL-UCLAF (FR) 1976-12-14 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-20100305353-A1 METHOD FOR PRODUCING PURIFIED FORMYLCYCLOPROPANE COMPOUND AND INTERMEDIATE OF SUCH FORMYLCYCLOPROPANE COMPOUND FPR1, FPR2, DHPS LMNA 4220/4885APLNR 1576/4885UGT2B7 2075/4885
US-20050090685-A1 Process for production of 3,3-dimethyl-2-formylcyclopropanecarboxylic acid derivatives ADSL, CMPK1, MRPL21 LMNA 4209/4885APLNR 1708/4885UGT2B7 706/4885

“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.