SCHEMBL12395121

SCHEMBL12395121

CC1=C(O)C(=O)C=C2C1=CC=C1[C@@]2(C)CC[C@@]2(C)[C@@H]3C[C@](C)(C(=O)OCc4ccccc4)CC[C@]3(C)CC[C@]12C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HSP90AB1 P08238 6/20 1.00
CASP3 P42574 6/20 1.00
CDC37 Q16543 6/20 1.00
NR4A1 P22736 6/20 0.81
TERT O14746 3/20 0.81
PRDX1 Q06830 1/20 0.76
PTPN1 P18031 1/20 0.75
CASP1 P29466 1/20 0.75
ABHD6 Q9BV23 1/20 0.75
KDM4E B2RXH2 1/20 0.75
TP53 P04637 1/20 0.75
CYP3A4 P08684 1/20 0.75
MAPT P10636 1/20 0.75
HPGD P15428 1/20 0.75
ALOX15 P16050 1/20 0.75
ALOX12 P18054 1/20 0.75
MAPK1 P28482 1/20 0.75
SMN1; SMN2 Q16637 1/20 0.75
TDP1 Q9NUW8 1/20 0.75
HSP90AA1 P07900 1/20 0.75

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
SCHEMBL18782351 0.92 HSP90AB1 (0.86) HSP90AB1CASP3CDC37NR4A1TERT
SCHEMBL22011612 0.92 CASP3 (0.86) HSP90AB1CASP3CDC37NR4A1TERT
SCHEMBL22011082 0.90 HSP90AB1 (0.82) HSP90AB1CASP3CDC37NR4A1TERT
SCHEMBL12395123 0.89 NR4A1 (1.00) HSP90AB1CASP3CDC37NR4A1TERT
SCHEMBL22010853 0.89 CASP3 (0.80) HSP90AB1CASP3CDC37NR4A1TERT
SCHEMBL18782134 0.87 HSP90AB1 (0.86) HSP90AB1CASP3CDC37NR4A1TERT
SCHEMBL13201839 0.87 NR4A1 (0.80) HSP90AB1CASP3CDC37NR4A1TERT
SCHEMBL20371640 0.86 NR4A1 (0.84) HSP90AB1CASP3CDC37NR4A1TERT
SCHEMBL22011610 0.86 NR4A1 (0.81) HSP90AB1CASP3CDC37NR4A1TERT
SCHEMBL18781835 0.86 TERT (0.77) HSP90AB1CASP3CDC37NR4A1TERT

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-11753436-B2 Analogs of celastrol ERX PHARMACEUTICALS CORPORATION (US) 2023-09-12 US disclosed
US-11753436-B2 Analogs of celastrol ERX PHARMACEUTICALS CORPORATION (US) 2023-09-12 US disclosed
US-20210061851-A1 ANALOGS OF CELASTROL ERX PHARMACEUTICALS CORPORATION 2021-03-04 US disclosed
US-10808005-B2 Ligand for orphan nuclear receptor Nur77 and uses thereof IXMEDICINE (XIAMEN) BIOLOGICAL TECHNOLOGY COMPANY LIMITED (CN) 2020-10-20 US disclosed
US-10662218-B2 Analogs of celastrol ERX PHARMACEUTICALS CORPORATION 2020-05-26 US disclosed
US-20190330261-A1 LIGAND FOR ORPHAN NUCLEAR RECEPTOR NUR77 AND USES THEREOF XIAMEN UNIVERSITY (CN) 2019-10-31 US disclosed
EP-3480207-A1 ORPHAN NUCLEAR RECEPTOR NUR77 LIGAND AND APPLICATION THEREOF Xiamen University (CN) 2019-05-08 EP disclosed
US-20110166216-A1 Compositions and Methods for Inhibiting Growth and Metastasis of Melanoma BURNHAM INSTITUTE FOR MEDICAL RESEARCH 2011-07-07 US disclosed
US-7888355-B2 Compositions and methods for inhibiting growth and metastasis of melanoma BURNHAM INSTITUTE FOR MEDICAL RESEARCH (US) 2011-02-15 US disclosed
US-20100305129-A1 COMPOSITIONS AND METHODS FOR INHIBITING GROWTH AND METASTASIS OF MELANOMA BURNHAM INSTITUTE FOR MEDICAL RESEARCH (US) 2010-12-02 US disclosed
US-7776894-B2 Compositions and methods for inhibiting growth and metastasis of melanoma BURNHAM INSTITUTE FOR MEDICAL RESEARCH (US) 2010-08-17 US disclosed
WO-2009026163-A1 COMPOSITIONS AND METHODS FOR INHIBITING GROWTH AND METASTASIS OF MELANOMA BURNHAM INSTITUTE FOR MEDICAL RESEARCH (US) 2009-02-26 WO disclosed
US-20090054438-A1 COMPOSITIONS AND METHODS FOR INHIBITING GROWTH AND METASTASIS OF MELANOMA BURNHAM INSTITUTE FOR MEDICAL RESEARCH (US) 2009-02-26 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 (8 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-20210061851-A1 ANALOGS OF CELASTROL GIPR, GPR119, EBP HSP90AB1 191/4885CASP3 247/4885CDC37 310/4885
US-10808005-B2 Ligand for orphan nuclear receptor Nur77 and uses thereof NR2E3, NR0B1, NR0B2 HSP90AB1 2423/4885CASP3 4286/4885CDC37 3351/4885
US-20100305129-A1 COMPOSITIONS AND METHODS FOR INHIBITING GROWTH AND METASTASIS OF MELANOMA API5, ACIN1, MCL1 HSP90AB1 116/4885CASP3 16/4885CDC37 732/4885
US-10662218-B2 Analogs of celastrol GIPR, GPR119, EBP HSP90AB1 191/4885CASP3 247/4885CDC37 310/4885
US-11753436-B2 Analogs of celastrol GIPR, GPR119, EBP HSP90AB1 191/4885CASP3 247/4885CDC37 310/4885
US-20190330261-A1 LIGAND FOR ORPHAN NUCLEAR RECEPTOR NUR77 AND USES THEREOF NR2E3, NR0B1, NR0B2 HSP90AB1 2423/4885CASP3 4286/4885CDC37 3351/4885
US-20090054438-A1 COMPOSITIONS AND METHODS FOR INHIBITING GROWTH AND METASTASIS OF MELANOMA API5, ACIN1, MCL1 HSP90AB1 116/4885CASP3 16/4885CDC37 732/4885
US-20110166216-A1 Compositions and Methods for Inhibiting Growth and Metastasis of Melanoma API5, ACIN1, MCL1 HSP90AB1 116/4885CASP3 16/4885CDC37 732/4885

“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.