Dopamine

Dopamine

SCHEMBL3290199

CC(C)=O.NCCc1ccc(O)c(O)c1

nearest known ligand 0.81

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRB1

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 4/20 0.81
MAPT P10636 4/20 0.81
MAPK1 P28482 3/20 0.81
TAAR1 Q96RJ0 3/20 0.81
ALDH1A1 P00352 3/20 0.81
ADRA2A P08913 2/20 0.81
DRD2 P14416 2/20 0.81
DRD1 P21728 2/20 0.81
DRD4 P21917 2/20 0.81
DRD5 P21918 2/20 0.81
SLC6A2 P23975 2/20 0.81
DRD3 P35462 2/20 0.81
RECQL P46063 2/20 0.81
SLC6A3 Q01959 2/20 0.81
TDP1 Q9NUW8 2/20 0.81
PTGS1 P23219 2/20 0.81
HIF1A Q16665 2/20 0.81
HSD17B10 Q99714 2/20 0.81
ALOX15 P16050 2/20 0.81
APEX1 P27695 2/20 0.81

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
Dopamine SCHEMBL3289315 0.94 KDM4E (0.78) KDM4EMAPTMAPK1TAAR1ALDH1A1
Dopamine SCHEMBL11668670 0.94 KDM4E (0.78) KDM4EMAPTMAPK1TAAR1ALDH1A1
Dopamine SCHEMBL28657094 0.94 KDM4E (0.78) KDM4EMAPTMAPK1TAAR1ALDH1A1
Dopamine SCHEMBL29082658 0.91 KDM4E (0.72) KDM4EMAPTMAPK1TAAR1ALDH1A1
Dopamine SCHEMBL28995038 0.90 KDM4E (0.84) KDM4EMAPTMAPK1TAAR1ALDH1A1
Dopamine SCHEMBL30355306 0.90 KDM4E (0.84) KDM4EMAPTMAPK1TAAR1ALDH1A1
Dopamine SCHEMBL9051903 0.90 KDM4E (0.84) KDM4EMAPTMAPK1TAAR1ALDH1A1
Dopamine SCHEMBL27987867 0.90 MAPK1 (0.91) KDM4EMAPTMAPK1TAAR1ALDH1A1
Dopamine SCHEMBL18159501 0.90 KDM4E (1.00) KDM4EMAPTMAPK1TAAR1ALDH1A1
Dopamine SCHEMBL8505 0.90 KDM4E (1.00) KDM4EMAPTMAPK1TAAR1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20130030192-A1 Method of Synthesizing Acetonide-Protected Catechol-Containing Compounds and Intermediates Produced Therein NORTHWESTERN UNIVERSITY 2013-01-31 US claimed
US-20100087622-A1 Method of Synthesizing Acetonide-Protected Catechol-Containing Compounds and Intermediates Produced Therein NORTHWESTERN UNIVERSITY (US) 2010-04-08 US claimed
US-11325112-B2 Method of forming inorganic nanocages RESEARCH FOUNDATION OF THE CITY UNIVERSITY OF NEW YORK (US) 2022-05-10 US disclosed
CN-110444411-B Conductive organic polymer coated phenolic resin matrix porous carbon composite material 河北省科学院能源研究所 2021-08-17 CN disclosed
US-20200346198-A1 METHOD OF FORMING INORGANIC NANOCAGES RESEARCH FOUNDATION OF THE CITY UNIVERSITY OF NEW YORK 2020-11-05 US disclosed
WO-2019178547-A1 BENZOXAZINE POLYMERS AND METHODS OF MAKING AND USING THE SAME THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2019-09-19 WO disclosed
US-20170282252-A1 METHOD OF FORMING INORGANIC NANOCAGES RESEARCH FOUNDATION OF THE CITY UNIVERSITY OF NEW YORK 2017-10-05 US disclosed
US-20130030192-A1 Method of Synthesizing Acetonide-Protected Catechol-Containing Compounds and Intermediates Produced Therein NORTHWESTERN UNIVERSITY 2013-01-31 US disclosed
US-8227628-B2 Method of synthesizing acetonide-protected catechol-containing compounds and intermediates produced therein NORTHWESTERN UNIVERSITY (US) 2012-07-24 US disclosed
US-20100087622-A1 Method of Synthesizing Acetonide-Protected Catechol-Containing Compounds and Intermediates Produced Therein NORTHWESTERN UNIVERSITY (US) 2010-04-08 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-20100087622-A1 Method of Synthesizing Acetonide-Protected Catechol-Containing Compounds and Intermediates Produced Therein DBH, COMT, PAH KDM4E 2054/4885MAPT 3973/4885MAPK1 2641/4885
US-20130030192-A1 Method of Synthesizing Acetonide-Protected Catechol-Containing Compounds and Intermediates Produced Therein DBH, COMT, PAH KDM4E 2054/4885MAPT 3973/4885MAPK1 2641/4885

“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.