Paricalcitol

Paricalcitol

SCHEMBL12535671

C[C@H](/C=C/[C@H](C)C(C)(C)O)C1CCC2/C(=C/C=C3C[C@@H](O)C[C@H](O)C3)CCC[C@@]21C

nearest known ligand 0.68

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

VDR

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

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ VDR known ✓ P11473 13/20 0.68
▸ HDAC6 Q9UBN7 4/20 0.60
▸ HDAC3 O15379 3/20 0.60
▸ HDAC2 Q92769 2/20 0.60
▸ NR1I2 O75469 2/20 0.57
▸ PGR P06401 2/20 0.57
▸ MEN1 O00255 1/20 0.57
▸ KMT2A Q03164 1/20 0.57
▸ HTR1A P08908 1/20 0.56
▸ ADORA3 P0DMS8 1/20 0.56
▸ SLC6A2 P23975 1/20 0.56
▸ SLC6A4 P31645 1/20 0.56
▸ ADRA1A P35348 1/20 0.56
▸ PTGS2 P35354 1/20 0.56

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
Paricalcitol SCHEMBL12915640 1.00 VDR (0.68) VDRHDAC6HDAC3HDAC2NR1I2
Paricalcitol SCHEMBL14491013 1.00 VDR (0.68) VDRHDAC6HDAC3HDAC2NR1I2
Paricalcitol SCHEMBL12464943 1.00 VDR (0.68) VDRHDAC6HDAC3HDAC2NR1I2
Paricalcitol SCHEMBL12397908 1.00 VDR (0.68) VDRHDAC6HDAC3HDAC2NR1I2
Paricalcitol SCHEMBL25447329 1.00 VDR (0.68) VDRHDAC6HDAC3HDAC2NR1I2
Paricalcitol SCHEMBL21836180 1.00 VDR (0.68) VDRHDAC6HDAC3HDAC2NR1I2
Paricalcitol SCHEMBL24066861 1.00 VDR (0.68) VDRHDAC6HDAC3HDAC2NR1I2
Paricalcitol SCHEMBL6945983 1.00 VDR (0.68) VDRHDAC6HDAC3HDAC2NR1I2
Paricalcitol SCHEMBL17354891 1.00 VDR (0.68) VDRHDAC6HDAC3HDAC2NR1I2
Paricalcitol SCHEMBL12553223 1.00 VDR (0.68) VDRHDAC6HDAC3HDAC2NR1I2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230026855-A1 COMPOSITIONS AND METHODS FOR TREATMENT OF PRE-CANCEROUS SKIN LESIONS WASHINGTON UNIVERSITY 2023-01-26 — — US disclosed
EP-3939593-A1 COMPOSITIONS AND METHODS FOR TREATMENT OF PRE-CANCEROUS SKIN LESIONS Washington University (US) 2022-01-19 — — EP disclosed
US-20210128732-A1 COMPOSITIONS AND METHODS FOR TREATMENT OF PRE-CANCEROUS SKIN LESIONS NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2021-05-06 — — US disclosed
US-10905763-B2 Compositions and methods for treatment of pre-cancerous skin lesions WASHINGTON UNIVERSITY 2021-02-02 — — US disclosed
US-20170246299-A1 COMPOSITIONS AND METHODS FOR TREATMENT OF PRE-CANCEROUS SKIN LESIONS WASHINGTON UNIVERSITY 2017-08-31 — — US disclosed
US-20170246299-A1 COMPOSITIONS AND METHODS FOR TREATMENT OF PRE-CANCEROUS SKIN LESIONS WASHINGTON UNIVERSITY 2017-08-31 — — US disclosed
US-20130006003-A1 NEW SYNTHONES FOR PREPARATION OF 19-NOR VITAMIN D DERIVATIVES INSTYTUT FARMACEUTYCZNY (PL) 2013-01-03 — — US disclosed
US-20130006003-A1 NEW SYNTHONES FOR PREPARATION OF 19-NOR VITAMIN D DERIVATIVES INSTYTUT FARMACEUTYCZNY (PL) 2013-01-03 — — US disclosed
US-20110137058-A1 PREPARATION OF PARICALCITOL FORMOSA LABORATORIES, INC. (TW) 2011-06-09 — — US disclosed
US-20110137058-A1 PREPARATION OF PARICALCITOL FORMOSA LABORATORIES, INC. (TW) 2011-06-09 — — US disclosed
WO-2011016739-A2 NEW SYNTHONES FOR PREPARATION OF 19-NOR VITAMIN D DERIVATIVES INSTYTUT FARMACEUTYCZNY (PL) 2011-02-10 — — WO disclosed
US-20090275768-A1 Preparation of Paricalcitol FORMOSA LABORATORIES, INC. (TW) 2009-11-05 — — US disclosed
US-20090275768-A1 Preparation of Paricalcitol FORMOSA LABORATORIES, INC. (TW) 2009-11-05 — — 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 (7 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-20110137058-A1 PREPARATION OF PARICALCITOL PTH1R, CYP24A1, CALCR VDR 13/4885HDAC6 4472/4885HDAC3 4225/4885
US-10905763-B2 Compositions and methods for treatment of pre-cancerous skin lesions TSLP, TP53, MKI67 VDR 404/4885HDAC6 3558/4885HDAC3 4023/4885
US-20230026855-A1 COMPOSITIONS AND METHODS FOR TREATMENT OF PRE-CANCEROUS SKIN LESIONS TSLP, TP53, MKI67 VDR 404/4885HDAC6 3558/4885HDAC3 4023/4885
US-20170246299-A1 COMPOSITIONS AND METHODS FOR TREATMENT OF PRE-CANCEROUS SKIN LESIONS TSLP, TP53, MKI67 VDR 404/4885HDAC6 3558/4885HDAC3 4023/4885
US-20130006003-A1 NEW SYNTHONES FOR PREPARATION OF 19-NOR VITAMIN D DERIVATIVES CYP24A1, CYP2R1, VDR VDR 3/4885HDAC6 3588/4885HDAC3 1891/4885
US-20090275768-A1 Preparation of Paricalcitol PTH1R, CYP24A1, CALCR VDR 13/4885HDAC6 4472/4885HDAC3 4225/4885
US-20210128732-A1 COMPOSITIONS AND METHODS FOR TREATMENT OF PRE-CANCEROUS SKIN LESIONS TSLP, TP53, MKI67 VDR 404/4885HDAC6 3558/4885HDAC3 4023/4885

“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.

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