SCHEMBL249681

SCHEMBL249681

CC1(C)C(/C=C/C=C/C=C/C=C2/N(CCCCCC(=O)O)c3ccc4ccccc4c3C2(C)C)=[N+](CCCCS(=O)(=O)O)c2ccc3ccccc3c21

nearest known ligand 0.83

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MLNR O43193 1/20 0.83
NR1I2 O75469 1/20 0.83
PGR P06401 1/20 0.83
ADRB1 P08588 1/20 0.83
ADORA3 P0DMS8 1/20 0.83
CHRM1 P11229 1/20 0.83
DRD2 P14416 1/20 0.83
ADRA2B P18089 1/20 0.83
ADRA2C P18825 1/20 0.83
CHRM3 P20309 1/20 0.83
CNR1 P21554 1/20 0.83
DRD1 P21728 1/20 0.83
TBXA2R P21731 1/20 0.83
SLC6A2 P23975 1/20 0.83
HRH2 P25021 1/20 0.83
HTR2C P28335 1/20 0.83
BDKRB2 P30411 1/20 0.83
ADORA1 P30542 1/20 0.83
AGTR1 P30556 1/20 0.83
SLC6A4 P31645 1/20 0.83

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
SCHEMBL20042445 1.00 MLNR (0.83) MLNRNR1I2PGRADRB1ADORA3
SCHEMBL16813068 0.99 MLNR (0.84) MLNRNR1I2PGRADRB1ADORA3
SCHEMBL17958827 0.95 MLNR (0.81) MLNRNR1I2PGRADRB1ADORA3
SCHEMBL13749987 0.95 MLNR (0.81) MLNRNR1I2PGRADRB1ADORA3
SCHEMBL14597388 0.95 BLM (0.75) MLNRNR1I2PGRADRB1ADORA3
SCHEMBL13657407 0.95 BLM (0.75) MLNRNR1I2PGRADRB1ADORA3
SCHEMBL19569765 0.94 MLNR (0.83) MLNRNR1I2PGRADRB1ADORA3
SCHEMBL16597109 0.94 CHRM1 (0.83) MLNRNR1I2PGRADRB1ADORA3
SCHEMBL17658757 0.94 CHRM1 (0.83) MLNRNR1I2PGRADRB1ADORA3
Bromide SCHEMBL31621175 0.94 BLM (0.74) MLNRNR1I2PGRADRB1ADORA3

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-20160067359-A1 COMPOSITION HAVING DYE AND CONJUGATE OF POLYETHYLENEGLYCOL AND ADDITIVE AND CONTRAST AGENT FOR PHOTOACOUSTIC IMAGING HAVING THE SAME CANON KABUSHIKI KAISHA (JP) 2016-03-10 US disclosed
US-9249306-B2 Quenched dendrimeric dyes for florescence detection CARNEGIE MELLON UNIVERSITY (US) 2016-02-02 US disclosed
US-8343463-B2 Optical imaging agent NUMIRA BIOSCIENCES INC. (US) 2013-01-01 US disclosed
US-20120058494-A1 Quenched Dendrimeric Dyes for Florescence Detection CARNEGIE MELLON UNIVERSITY (US) 2012-03-08 US disclosed
US-20110027191-A1 OPTICAL IMAGING AGENT NUMIRA BIOSCIENCES, INC. (US) 2011-02-03 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 (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-20160067359-A1 COMPOSITION HAVING DYE AND CONJUGATE OF POLYETHYLENEGLYCOL AND ADDITIVE AND CONTRAST AGENT FOR PHOTOACOUSTIC IMAGING HAVING THE SAME ALG1, PHOSPHO1, COL1A1 MLNR 1078/4885NR1I2 1147/4885PGR 2132/4885
US-20110027191-A1 OPTICAL IMAGING AGENT TNNC1, TNNI3, MB MLNR 1187/4885NR1I2 2024/4885PGR 4045/4885
US-20120058494-A1 Quenched Dendrimeric Dyes for Florescence Detection FAP, APC, ANXA6 MLNR 385/4885NR1I2 4400/4885PGR 4572/4885

“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.