SCHEMBL2670053

SCHEMBL2670053

OCCNCc1cccc(O)c1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC2A4 P14672 1/20 0.59
CYP1A2 P05177 1/20 0.58
CYP3A4 P08684 1/20 0.58
PKM P14618 1/20 0.58
ALOX15 P16050 1/20 0.58
NFKB1 P19838 1/20 0.58
MAPK1 P28482 1/20 0.58
KMT2A Q03164 1/20 0.56
KDM4E B2RXH2 1/20 0.56
LMNA P02545 1/20 0.56
MAPT P10636 1/20 0.56
BLM P54132 1/20 0.56
PMP22 Q01453 1/20 0.56
DRD2 P14416 1/20 0.51
DRD4 P21917 1/20 0.51
ADRA1D P25100 1/20 0.51
ADRA1A P35348 1/20 0.51
ADRA1B P35368 1/20 0.51
DRD3 P35462 1/20 0.51
HTR2A P28223 2/20 0.49

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
SCHEMBL6254596 0.90 SLC2A4 (0.65) SLC2A4CYP1A2CYP3A4PKMALOX15
SCHEMBL10859843 0.88 PDCD1 (0.53) KMT2APDCD1CD274SMN1; SMN2
SCHEMBL9416529 0.86 SLC2A4 (0.75) SLC2A4CYP1A2CYP3A4PKMALOX15
SCHEMBL8584527 0.83 SLC2A4 (0.57) SLC2A4CYP1A2CYP3A4PKMALOX15
Phenol SCHEMBL28156093 0.82 DRD4 (0.47) CYP1A2CYP3A4PKMALOX15NFKB1
Resorcinol SCHEMBL10800197 0.81 CYP3A4 (0.57) CYP1A2CYP3A4PKMALOX15NFKB1
SCHEMBL17285992 0.80 CYP1A2 (0.58) SLC2A4CYP1A2CYP3A4PKMALOX15
SCHEMBL7023370 0.79 ENPP2 (0.47) CYP3A4NFKB1KMT2AENPP2PDCD1
SCHEMBL16619429 0.79 CYP1A2 (0.61) CYP1A2KDM4EPDCD1CD274SMN1; SMN2
SCHEMBL14294259 0.79 PDCD1 (0.50) CYP1A2LMNAPDCD1CD274SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8455692-B2 Process for resolution of 1-(3-hydroxyphenyl)-2-methylamino ethanol Divi's Laboratories, Ltd. (IN) 2013-06-04 US claimed
US-20120108848-A1 PROCESS FOR RESOLUTION OF 1-(3-HYDROXYPHENYL)-2-METHYLAMINO ETHANOL DIVI'S LABORATORIES LIMITED (IN) 2012-05-03 US claimed
EP-4543397-A1 COMPOSITION FOR LIGHTENING KERATIN FIBRES AND PROCESS FOR LIGHTENING KERATIN FIBRES USING SAID COMPOSITION L'OREAL (FR) 2025-04-30 EP disclosed
EP-4543399-A1 COMPOSITION FOR LIGHTENING KERATIN FIBRES AND PROCESS FOR LIGHTENING KERATIN FIBRES USING SAID COMPOSITION L'OREAL (FR) 2025-04-30 EP disclosed
EP-4543398-A1 COMPOSITION FOR LIGHTENING KERATIN FIBRES AND PROCESS FOR LIGHTENING KERATIN FIBRES USING SAID COMPOSITION L'OREAL (FR) 2025-04-30 EP disclosed
EP-4543396-A1 COMPOSITION FOR LIGHTENING KERATIN FIBRES AND PROCESS FOR LIGHTENING KERATIN FIBRES USING SAID COMPOSITION L'OREAL (FR) 2025-04-30 EP disclosed
WO-2023247616-A1 COMPOSITION FOR LIGHTENING KERATIN FIBRES AND PROCESS FOR LIGHTENING KERATIN FIBRES USING SAID COMPOSITION L'OREAL (FR) 2023-12-28 WO disclosed
WO-2023247618-A1 COMPOSITION FOR LIGHTENING KERATIN FIBRES AND PROCESS FOR LIGHTENING KERATIN FIBRES USING SAID COMPOSITION L'OREAL (FR) 2023-12-28 WO disclosed
WO-2023247615-A1 COMPOSITION FOR LIGHTENING KERATIN FIBRES AND PROCESS FOR LIGHTENING KERATIN FIBRES USING SAID COMPOSITION L'OREAL (FR) 2023-12-28 WO disclosed
WO-2023247610-A1 COMPOSITION FOR LIGHTENING KERATIN FIBRES AND PROCESS FOR LIGHTENING KERATIN FIBRES USING SAID COMPOSITION L'OREAL (FR) 2023-12-28 WO disclosed
EP-2640713-A1 ASCORBIC ACID DERIVATIVES AS OXIDATION DYE COMPONENTS Merck Patent GmbH (DE) 2013-09-25 EP disclosed
US-8455692-B2 Process for resolution of 1-(3-hydroxyphenyl)-2-methylamino ethanol Divi's Laboratories, Ltd. (IN) 2013-06-04 US disclosed
US-8455692-B2 Process for resolution of 1-(3-hydroxyphenyl)-2-methylamino ethanol Divi's Laboratories, Ltd. (IN) 2013-06-04 US disclosed
US-8455692-B2 Process for resolution of 1-(3-hydroxyphenyl)-2-methylamino ethanol Divi's Laboratories, Ltd. (IN) 2013-06-04 US disclosed
WO-2012065685-A1 ASCORBIC ACID DERIVATIVES AS OXIDATION DYE COMPONENTS MERCK PATENT GMBH (DE) 2012-05-24 WO disclosed
US-20120108848-A1 PROCESS FOR RESOLUTION OF 1-(3-HYDROXYPHENYL)-2-METHYLAMINO ETHANOL DIVI'S LABORATORIES LIMITED (IN) 2012-05-03 US disclosed
US-20120108848-A1 PROCESS FOR RESOLUTION OF 1-(3-HYDROXYPHENYL)-2-METHYLAMINO ETHANOL DIVI'S LABORATORIES LIMITED (IN) 2012-05-03 US disclosed
US-20120108848-A1 PROCESS FOR RESOLUTION OF 1-(3-HYDROXYPHENYL)-2-METHYLAMINO ETHANOL DIVI'S LABORATORIES LIMITED (IN) 2012-05-03 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 (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-20120108848-A1 PROCESS FOR RESOLUTION OF 1-(3-HYDROXYPHENYL)-2-METHYLAMINO ETHANOL ADH1A, CYP2E1, ADH1C SLC2A4 4602/4885CYP1A2 13/4885CYP3A4 74/4885

“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.