SCHEMBL412018

SCHEMBL412018

O=C(O)[C@H](O)CNc1ccccc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 5/20 0.50
SMN1; SMN2 Q16637 3/20 0.49
HTT P42858 1/20 0.49
DNM1 Q05193 1/20 0.45
LMNA P02545 3/20 0.44
KDM4E B2RXH2 2/20 0.44
MEN1 O00255 2/20 0.44
KMT2A Q03164 2/20 0.44
PTPRA P18433 1/20 0.42
ALDH1A1 P00352 2/20 0.41
TP53 P04637 1/20 0.41
EPHX1 P07099 1/20 0.41
TSHR P16473 1/20 0.41
EPHX2 P34913 1/20 0.41
CDK9 P50750 1/20 0.41
CLK4 Q9HAZ1 1/20 0.41
ADRB2 P07550 1/20 0.41
ADRB1 P08588 1/20 0.41
ADRB3 P13945 1/20 0.41
CASP3 P42574 1/20 0.41

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
SCHEMBL555036 1.00 MAPT (0.50) MAPTSMN1; SMN2HTTDNM1LMNA
SCHEMBL239274 1.00 MAPT (0.50) MAPTSMN1; SMN2HTTDNM1LMNA
Hydrochloric Acid SCHEMBL1140275 0.98 MAPT (0.49) MAPTSMN1; SMN2HTTDNM1LMNA
Hydrochloric Acid SCHEMBL6422363 0.98 MAPT (0.49) MAPTSMN1; SMN2HTTDNM1LMNA
Phosphoric Acid SCHEMBL8362755 0.85 MAPT (0.43) MAPTSMN1; SMN2HTTDNM1LMNA
SCHEMBL5514976 0.83 MAPT (0.48) MAPTSMN1; SMN2HTTDNM1LMNA
SCHEMBL12227832 0.82 FDPS (0.54) SMN1; SMN2HTTLMNAKDM4EPTPRA
SCHEMBL14157786 0.82 MAPT (0.44) MAPTHTTLMNAKDM4EMEN1
Hydrochloric Acid SCHEMBL4829746 0.81 MAPT (0.42) MAPTHTTLMNAKDM4EMEN1
SCHEMBL6086624 0.81 MAPT (0.57) MAPTSMN1; SMN2HTTDNM1LMNA

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 106 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8633326-B2 Method for preparing taxane derivatives SAMYANG BIOPHARMACEUTICALS CORPORATION (KR) 2014-01-21 US claimed
US-20120035379-A1 METHOD FOR PREPARING TAXANE DERIVATIVES SAMYANG GENEX CORPORATION (KR) 2012-02-09 US claimed
WO-2010123186-A1 METHOD FOR PREPARING TAXANE DERIVATIVES SAMYANG GENEX CORPORATION (KR) 2010-10-28 WO claimed
US-6130336-A Process for preparing paclitaxel HANMI PHARM., CO. LTD. (KR) 2000-10-10 US claimed
EP-0923565-A1 PROCESS FOR PREPARING PACLITAXEL HANMI PHARMACEUTICAL CO.,LTD. (KR) 1999-06-23 EP claimed
WO-1998008832-A1 PROCESS FOR PREPARING PACLITAXEL HANMI PHARM. CO., LTD. (KR) 1998-03-05 WO claimed
JP-1305076-A None JP disclosed
US-20260041775-A1 COMPOSITIONS FOR DRUG ADMINISTRATION AEGIS THERAPEUTICS, LLC (US) 2026-02-12 US disclosed
US-11173209-B2 Compositions for drug administration AEGIS THERAPEUTICS, LLC (US) 2021-11-16 US disclosed
US-20210121573-A1 ABSORPTION ENHANCERS FOR DRUG ADMINISTRATION AEGIS THERAPEUTICS, LLC 2021-04-29 US disclosed
US-20200138956-A1 COMPOSITIONS FOR DRUG ADMINISTRATION AEGIS THERAPEUTICS, LLC 2020-05-07 US disclosed
US-10265402-B2 Absorption enhancers for drug administration AEGIS THERAPEUTICS, LLC (US) 2019-04-23 US disclosed
US-20180221489-A1 ABSORPTION ENHANCERS FOR DRUG ADMINISTRATION AEGIS THERAPEUTICS, LLC 2018-08-09 US disclosed
WO-1996040667-A1 PACLITAXEL SYNTHESIS FROM PRECURSOR COMPOUNDS AND METHODS OF PRODUCING THE SAME NAPRO BIOTHERAPEUTICS, INC. (US) 1996-12-19 WO disclosed
WO-1996040666-A1 PACLITAXEL SYNTHESIS FROM PRECURSOR COMPOUNDS AND METHODS OF PRODUCING THE SAME NAPRO BIOTHERAPEUTICS, INC. (US) 1996-12-19 WO disclosed
WO-1996013495-A1 TAXOID DERIVATIVES, THEIR PREPARATION AND THEIR USE AS ANTITUMOR AGENTS THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 1996-05-09 WO disclosed
EP-0681568-A1 PROCESS FOR PREPARATION OF TAXANE DERIVATIVES AND $g(b)-LACTAM INTERMEDIATES THEREFOR THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 1995-11-15 EP disclosed
WO-1994018164-A1 PROCESS FOR PREPARATION OF TAXANE DERIVATIVES AND β-LACTAM INTERMEDIATES THEREFOR THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 1994-08-18 WO disclosed
US-5294737-A Hydrolysis, cyclization, condensation THE RESEARCH FOUNDATION STATE UNIVERSITY OF NEW YORK (US) 1994-03-15 US disclosed
JP-H01305076-A METHOD FOR PREPARING TAXOL CENTRE NATL RECH SCIENT <CNRS> 1989-12-08 JP 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-11173209-B2 Compositions for drug administration SLC10A1, ABCB11, CSGALNACT1 MAPT 2171/4885SMN1; SMN2 1045/4885HTT 593/4885
US-20120035379-A1 METHOD FOR PREPARING TAXANE DERIVATIVES PTMA, TNPO3, ACR MAPT 737/4885SMN1; SMN2 2678/4885HTT 2862/4885
US-20260041775-A1 COMPOSITIONS FOR DRUG ADMINISTRATION SLC2A8, SLC5A2, SLC2A4 MAPT 452/4885SMN1; SMN2 1656/4885HTT 1113/4885
US-20200138956-A1 COMPOSITIONS FOR DRUG ADMINISTRATION SLC10A1, ABCB11, CSGALNACT1 MAPT 2171/4885SMN1; SMN2 1045/4885HTT 593/4885

“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.