SCHEMBL18474331

SCHEMBL18474331

CC1(C)CCC(CN2CCN(c3ccc(C(=O)NSc4ccc(NCC5CCOCC5)c([N+](=O)[O-])c4)c(Oc4cnc5[nH]ccc5c4)c3)CC2)=C(c2ccc(Cl)cc2)C1

nearest known ligand 0.83

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ BCL2 P10415 20/20 0.83
▸ BCL2L1 Q07817 4/20 0.83
▸ MCL1 Q07820 2/20 0.83
▸ BCL2L2 Q92843 2/20 0.83
▸ NSD2 O96028 1/20 0.83
▸ ADORA3 P0DMS8 1/20 0.83
▸ CYP2C9 P11712 1/20 0.83
▸ ADRA2C P18825 1/20 0.83
▸ SLC6A2 P23975 1/20 0.83
▸ BID P55957 1/20 0.83
▸ SLC6A3 Q01959 1/20 0.83
▸ ASPH Q12797 1/20 0.83
▸ BAD Q92934 1/20 0.83
▸ NSD1 Q96L73 1/20 0.83
▸ NSD3 Q9BZ95 1/20 0.83
▸ TMEM97 Q5BJF2 1/20 0.74

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
SCHEMBL19503727 0.95 BCL2 (0.75) BCL2BCL2L1MCL1BCL2L2NSD2
SCHEMBL21233544 0.95 BCL2 (0.75) BCL2BCL2L1MCL1BCL2L2NSD2
SCHEMBL21573176 0.95 BCL2 (0.83) BCL2BCL2L1MCL1BCL2L2NSD2
SCHEMBL18635202 0.95 BCL2 (0.75) BCL2BCL2L1MCL1BCL2L2NSD2
SCHEMBL21573213 0.94 BCL2 (0.83) BCL2BCL2L1MCL1BCL2L2NSD2
SCHEMBL20368840 0.94 BCL2 (0.74) BCL2BCL2L1MCL1BCL2L2NSD2
SCHEMBL19504148 0.94 BCL2 (0.74) BCL2BCL2L1MCL1BCL2L2NSD2
SCHEMBL23489377 0.93 BCL2 (0.75) BCL2BCL2L1MCL1BCL2L2NSD2
SCHEMBL19939538 0.93 BCL2 (0.74) BCL2BCL2L1MCL1BCL2L2NSD2
SCHEMBL21851473 0.92 BCL2 (0.71) BCL2BCL2L1MCL1BCL2L2NSD2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4215197-A1 INHIBITING MUTANT IDH-1 Forma Therapeutics, Inc. (US) 2023-07-26 — — EP disclosed
US-20230066088-A1 INHIBITING MUTANT ISOCITRATE DEHYDROGENASE 1 (mIDH-1) FORMA THERAPEUTICS, INC. 2023-03-02 — — US disclosed
US-11576906-B2 Inhibiting mutant IDH-1 FORMA THERAPEUTICS, INC. (US) 2023-02-14 — — US disclosed
EP-3720442-B1 INHIBITING MUTANT IDH-1 FORMA THERAPEUTICS INC (US) 2022-12-28 — — EP disclosed
US-11376246-B2 Inhibiting mutant IDH-1 FORMA THERAPEUTICS, INC. (US) 2022-07-05 — — US disclosed
US-11311527-B2 Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1) FORMA THERAPEUTICS, INC. (US) 2022-04-26 — — US disclosed
US-20210196701-A1 INHIBITING MUTANT IDH-1 FORMA THERAPEUTICS, INC. 2021-07-01 — — US disclosed
WO-2021080955-A1 SUBSTITUTED 4-AMINOISOINDOLINE-1,3-DIONE COMPOUNDS AND SECOND ACTIVE AGENTS FOR COMBINED USE CELGENE CORPORATION (US) 2021-04-29 — — WO disclosed
WO-2020232381-A1 INHIBITING MUTANT ISOCITRATE DEHYDROGENASE 1 (mIDH-1) FORMA THERAPEUTICS, INC. (US) 2020-11-19 — — WO disclosed
US-20200297717-A1 INHIBITING MUTANT ISOCITRATE DEHYDROGENASE 1 (mIDH-1) FORMA THERAPEUTICS, INC. 2020-09-24 — — US disclosed
US-20200108060-A1 INHIBITING MUTANT IDH-1 FORMA THERAPEUTICS, INC. 2020-04-09 — — US disclosed
WO-2020023435-A1 VENETOCLAX BASIC SALTS AND PROCESSES FOR THE PURIFICATION OF VENETOCLAX ALBANY MOLECULAR RESEARCH, INC. (US) 2020-01-30 — — WO disclosed
US-20190350919-A1 INHIBITING MUTANT IDH-1 FORMA THERAPEUTICS, INC. 2019-11-21 — — US disclosed
WO-2019161221-A2 SELECTIVE BCL-2 INHIBITORS IN COMBINATION WITH AN ANTI-PD-1 OR AN ANTI-PD-L1 ANTIBODY FOR THE TREATMENT OF CANCERS ABBVIE INC. (US) 2019-08-22 — — WO disclosed
WO-2019150253-A1 SOLID STATE FORMS OF VENETOCLAX AND ITS PROCESS FOR THE PREPARATION THERE OF ALEMBIC PHARMACEUTICALS LIMITED (IN) 2019-08-08 — — WO disclosed
WO-2018127130-A1 COMPOUNDS AS BCL-2-SELECTIVE APOPTOSIS-INDUCING AGENTS SHANGHAI FOCHON PHARMACEUTICAL CO., LTD. (CN) 2018-07-12 — — WO disclosed
WO-2018029711-A2 PROCESS FOR THE PREPARATION OF VENETOCLAX MYLAN LABORATORIES LIMITED (IN) 2018-02-15 — — WO disclosed
EP-2643322-B1 SALTS AND CRYSTALLINE FORMS OF AN APOPTOSIS-INDUCING AGENT ABBVIE INC (US) 2017-08-30 — — EP disclosed
WO-2017023584-A1 COMBINATION THERAPIES FOR TREATING CANCERS GILEAD SCIENCES, INC. (US) 2017-02-09 — — WO 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-20210196701-A1 INHIBITING MUTANT IDH-1 IDH3A, IDH3B, IDH1 BCL2 701/4885BCL2L1 472/4885MCL1 10/4885
US-20190350919-A1 INHIBITING MUTANT IDH-1 IDH3A, IDH3B, IDH1 BCL2 701/4885BCL2L1 472/4885MCL1 10/4885
US-11376246-B2 Inhibiting mutant IDH-1 IDH3A, IDH3B, IDH1 BCL2 701/4885BCL2L1 472/4885MCL1 10/4885
US-11311527-B2 Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1) IDH1, IDH3B, IDH2 BCL2 1683/4885BCL2L1 770/4885MCL1 57/4885
US-20230066088-A1 INHIBITING MUTANT ISOCITRATE DEHYDROGENASE 1 (mIDH-1) IDH1, IDH3B, IDH2 BCL2 1683/4885BCL2L1 770/4885MCL1 57/4885
US-11576906-B2 Inhibiting mutant IDH-1 IDH3A, IDH3B, IDH1 BCL2 701/4885BCL2L1 472/4885MCL1 10/4885
US-20200108060-A1 INHIBITING MUTANT IDH-1 IDH3A, IDH3B, IDH1 BCL2 701/4885BCL2L1 472/4885MCL1 10/4885
US-20200297717-A1 INHIBITING MUTANT ISOCITRATE DEHYDROGENASE 1 (mIDH-1) IDH1, IDH3B, IDH2 BCL2 1683/4885BCL2L1 770/4885MCL1 57/4885

“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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