SCHEMBL1751899

SCHEMBL1751899

O=C(OC1(C(=O)c2ccccc2)C(=O)OC(=O)C1O)c1ccccc1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ F2 P00734 1/20 0.37
▸ LMNA P02545 1/20 0.37
▸ PPM1B O75688 1/20 0.36
▸ TSHR P16473 1/20 0.35
▸ GAA P10253 1/20 0.35
▸ KMT2A Q03164 5/20 0.34
▸ MAPT P10636 2/20 0.34
▸ SMN1; SMN2 Q16637 1/20 0.34
▸ MEN1 O00255 2/20 0.34
▸ HSD17B10 Q99714 1/20 0.34
▸ MAOA P21397 1/20 0.34
▸ MAOB P27338 1/20 0.34
▸ BCHE P06276 1/20 0.34
▸ NPC1 O15118 1/20 0.34
▸ RAB9A P51151 1/20 0.34
▸ ALDH1A1 P00352 1/20 0.33
▸ CYP1A2 P05177 1/20 0.33
▸ CYP2C9 P11712 1/20 0.33
▸ CYP2C19 P33261 1/20 0.33
▸ STAT3 P40763 1/20 0.33

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
SCHEMBL7410693 1.00 F2 (0.37) F2LMNAPPM1BTSHRGAA
SCHEMBL7415226 1.00 F2 (0.37) F2LMNAPPM1BTSHRGAA
SCHEMBL15903870 0.86 TDP1 (0.39) GAAKMT2AMAPTSMN1; SMN2RAB9A
SCHEMBL5692181 0.76 PKM (0.35) LMNAMAPTNPC1RAB9ACYP2C9
SCHEMBL30686187 0.71 LMNA (0.38) LMNATSHRGAAKMT2AMAPT
SCHEMBL10392788 0.66 LMNA (0.44) F2LMNATSHRGAAKMT2A
SCHEMBL636837 0.63 LMNA (0.48) F2LMNAPPM1BTSHRGAA
SCHEMBL1751897 0.63 LMNA (0.48) F2LMNAPPM1BTSHRGAA
SCHEMBL637664 0.63 LMNA (0.48) F2LMNAPPM1BTSHRGAA
SCHEMBL30526381 0.63 F2 (0.48) F2LMNATSHRGAAKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110452258-A A kind of preparation method of dipeptides valine Boroproline salt BALMXY PHARMACEUTIC CO LTD 2019-11-15 — — CN claimed
CN-106699812-A Method for preparation and purification of tenofovir prodrug 江苏豪森药业集团有限公司 2017-05-24 — — CN claimed
US-4259383-A PEROXY COMPOUNDS STERLING DRUG INC. (US) 1981-03-31 — — US claimed
CN-109738560-B Method for measuring content of tartaric acid optical isomer 宜昌人福药业有限责任公司 2020-11-03 — — CN disclosed
US-7968748-B2 Process for resolving racemic mixtures and a diastereoisomeric complex of a resolving agent and an enantiomer of interest ABIOGEN PHARMA S.P.A. (IT) 2011-06-28 — — US disclosed
US-20090292129-A1 PROCESS FOR RESOLVING RACEMIC MIXTURES AND A DIASTEREOISOMERIC COMPLEX OF A RESOLVING AGENT AND AN ENANTIOMER OF INTEREST ABIOGEN PHARMA S.P.A. (IT) 2009-11-26 — — US disclosed
EP-1986996-A2 A PROCESS FOR RESOLVING RACEMIC MIXTURES AND A DIASTEREOISOMERIC COMPLEX OF A RESOLVING AGENT AND AN ENANTIOMER OF INTEREST Abiogen Pharma S.p.A. (IT) 2008-11-05 — — EP disclosed
WO-2007088571-A2 A PROCESS FOR RESOLVING RACEMIC MIXTURES AND A DIASTEREOISOMERIC COMPLEX OF A RESOLVING AGENT AND AN ENANTIOMER OF INTEREST ABIOGEN PHARMA S.P.A. (IT) 2007-08-09 — — WO disclosed
JP-2003335766-A METHOD FOR PRODUCING DIBENZOYLTARTARIC ACID AND ACID ANHYDRIDE THEREOF NIPPON LIGHT METAL CO LTD 2003-11-28 — — JP disclosed
EP-0256586-B1 PROCESS FOR THE PREPARATION OF ESTERS OF 4-(2,3-EPOXYPROPOXY)PHENYLACETIC ACID AND 4-(2-HYDROXY-3-ISOPROPYLAMINO-PROPOXY)PHENYLACETIC ACID AND/OR ATENOLOL IN STEREOSPECIFIC FORM GIST-BROCADES N.V. (NL) 1992-05-13 — — EP disclosed
EP-0256586-A1 Process for the preparation of esters of 4-(2,3-epoxypropoxy)phenylacetic acid and 4-(2-hydroxy-3-isopropylamino-propoxy)phenylacetic acid and/or atenolol in stereospecific form GIST-BROCADES N.V. (NL) 1988-02-24 — — EP disclosed
US-4259383-A PEROXY COMPOUNDS STERLING DRUG INC. (US) 1981-03-31 — — 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-20090292129-A1 PROCESS FOR RESOLVING RACEMIC MIXTURES AND A DIASTEREOISOMERIC COMPLEX OF A RESOLVING AGENT AND AN ENANTIOMER OF INTEREST SRR, EPHX2, ALOX5 F2 153/4885LMNA 715/4885PPM1B 4065/4885

“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.

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