Dimethylformamide

Dimethylformamide

SCHEMBL2678657

CCO.CN(C)C=O.CO

nearest known ligand 0.60

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MMP1MMP13MMP7MMP8polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Dimethylformamide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.60
ALDH1A1 P00352 2/20 0.40
USP2 O75604 1/20 0.36
ALOX15 P16050 1/20 0.36
MAPK1 P28482 1/20 0.33
TDP1 Q9NUW8 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
Dimethylformamide SCHEMBL849515 0.97
Dimethylformamide SCHEMBL28317966 0.93 TSHR (0.60) TSHRALDH1A1USP2ALOX15MAPK1
Dimethylformamide SCHEMBL11302637 0.93
Dimethylformamide SCHEMBL3457497 0.93
Dimethylformamide SCHEMBL10405953 0.88 TSHR (0.53) TSHRALDH1A1USP2ALOX15MAPK1
Dimethylformamide SCHEMBL850064 0.86
Dimethylformamide SCHEMBL11264821 0.85 TSHR (0.50) TSHRALDH1A1USP2ALOX15TDP1
Dimethylformamide SCHEMBL8801229 0.84
Dimethylformamide SCHEMBL23282482 0.83 TSHR (0.47) TSHRALDH1A1USP2ALOX15
Ether SCHEMBL8913501 0.83 TSHR (0.47) TSHRALDH1A1USP2ALOX15

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10766915-B2 Metal-based coordination complexes as photodynamic compounds and their use MCFARLAND SHERRI ANN (CA) 2020-09-08 US disclosed
US-20160039854-A1 METAL-BASED COORDINATION COMPLEXES AS PHOTODYNAMIC COMPOUNDS AND THEIR USE MCFARLAND SHERRI ANN (CA) 2016-02-11 US disclosed
US-8173642-B2 Aminodihydrothiazine derivatives SHIONOGI & CO., LTD. (JP) 2012-05-08 US disclosed
US-20090082560-A1 AMINODIHYDROTHIAZINE DERIVATIVES SHIONOGI & CO., LTD. (JP) 2009-03-26 US disclosed
US-20060166982-A1 Isotopically labelly indlinone derivatives and process for their preparation PFIZER ITALIA S.R.L. (IT) 2006-07-27 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 (4 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-20160039854-A1 METAL-BASED COORDINATION COMPLEXES AS PHOTODYNAMIC COMPOUNDS AND THEIR USE PIN1, PPIF, PPOX TSHR 4598/4885ALDH1A1 2483/4885USP2 4124/4885
US-10766915-B2 Metal-based coordination complexes as photodynamic compounds and their use PIN1, PPIF, PPOX TSHR 4598/4885ALDH1A1 2483/4885USP2 4124/4885
US-20060166982-A1 Isotopically labelly indlinone derivatives and process for their preparation CYP3A5, SLC10A2, TMEM14C TSHR 2996/4885ALDH1A1 440/4885USP2 4195/4885
US-20090082560-A1 AMINODIHYDROTHIAZINE DERIVATIVES BACE1, BACE2, APP TSHR 1912/4885ALDH1A1 1897/4885USP2 2418/4885

“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.