SCHEMBL4547845

SCHEMBL4547845

CC(C)c1ccc([N+](=O)[O-])c([N+](=O)[O-])c1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.55
CYP3A4 P08684 2/20 0.55
CASP6 P55212 1/20 0.46
MEN1 O00255 2/20 0.43
KMT2A Q03164 2/20 0.43
MAPT P10636 4/20 0.41
CYP1A2 P05177 2/20 0.41
CYP2C9 P11712 2/20 0.41
CYP2C19 P33261 2/20 0.41
ALDH1A1 P00352 2/20 0.40
MAPK1 P28482 2/20 0.40
HTT P42858 2/20 0.40
TP53 P04637 1/20 0.40
CYP2D6 P10635 1/20 0.40
STAT6 P42226 1/20 0.40
HIF1A Q16665 1/20 0.40
PHLPP2 Q6ZVD8 1/20 0.40
HSD17B10 Q99714 1/20 0.40
VCAM1 P19320 1/20 0.40
TDP1 Q9NUW8 3/20 0.39

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
SCHEMBL10608130 0.86 TSHR (0.59) TSHRCYP3A4CASP6MAPTCYP1A2
SCHEMBL20364501 0.84 PDK1 (0.55) TSHRCYP3A4MEN1KMT2AMAPT
SCHEMBL6234170 0.84 PDK1 (0.44) TSHRCYP3A4MEN1KMT2AMAPT
SCHEMBL2436243 0.84 TSHR (0.56) TSHRCYP3A4MEN1KMT2AMAPT
SCHEMBL12381771 0.84 MAPT (0.53) TSHRCYP3A4MEN1KMT2AMAPT
SCHEMBL5595045 0.82 GPR35 (0.56) TSHRCYP3A4MEN1KMT2AMAPT
SCHEMBL9886771 0.82 VCAM1 (0.55) CYP3A4MEN1KMT2AMAPTCYP1A2
SCHEMBL1455781 0.82 ALDH1A1 (0.50) TSHRCYP3A4MEN1KMT2AMAPT
SCHEMBL978898 0.82 TSHR (0.59) TSHRCYP3A4MEN1KMT2AMAPT
SCHEMBL1026668 0.82 ALDH1A1 (0.56) TSHRMEN1KMT2AMAPTCYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9151735-B2 Cyanine derivatives having meso-reactive functional group at polymethine chain and preparation method thereof EWHA UNIVERSITY-INDUSTRY COLLABORATION FOUNDATION (KR) 2015-10-06 US disclosed
US-8884032-B2 Trioxane monomers and dimers THE JOHNS HOPKINS UNIVERSITY (US) 2014-11-11 US disclosed
US-20140329331-A1 NOVEL CYANINE DERIVATIVES HAVING MESO-REACTIVE FUNCTIONAL GROUP AT POLYMETHINE CHAIN AND PREPARATION METHOD THEREOF EWHA UNIVERSITY-INDUSTRY COLLABORATION FOUNDATION (KR) 2014-11-06 US disclosed
US-8344180-B2 Hydrazine amide derivative SHIONOGI & CO., LTD. (JP) 2013-01-01 US disclosed
US-8344180-B2 Hydrazine amide derivative SHIONOGI & CO., LTD. (JP) 2013-01-01 US disclosed
US-20120108545-A1 Trioxane Monomers and Dimers THE JOHNS HOPKINS UNIVERSITY (US) 2012-05-03 US disclosed
US-20100004295-A1 Hydrazine amide derivative SHIONOGI & CO., LTD. 2010-01-07 US disclosed
US-20100004295-A1 Hydrazine amide derivative SHIONOGI & CO., LTD. 2010-01-07 US disclosed
EP-2062878-A1 HYDRAZINE AMIDE DERIVATIVE Shionogi&Co., Ltd. (JP) 2009-05-27 EP 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 (3 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-20120108545-A1 Trioxane Monomers and Dimers CDK10, TMSB10, CASP10 TSHR 1327/4885CYP3A4 561/4885CASP6 767/4885
US-20140329331-A1 NOVEL CYANINE DERIVATIVES HAVING MESO-REACTIVE FUNCTIONAL GROUP AT POLYMETHINE CHAIN AND PREPARATION METHOD THEREOF NTRK1, TYR, PARN TSHR 4179/4885CYP3A4 992/4885CASP6 996/4885
US-20100004295-A1 Hydrazine amide derivative NPY5R, NPY1R, NPY2R TSHR 48/4885CYP3A4 2866/4885CASP6 3074/4885

“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.