SCHEMBL7996639

SCHEMBL7996639

CC(C)C(=O)SCCCCCCC(=O)Nc1nc(-c2ccccc2)cs1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HDAC1 Q13547 10/20 0.67
▸ HDAC2 Q92769 8/20 0.67
▸ HDAC6 Q9UBN7 8/20 0.67
▸ HDAC9 Q9UKV0 7/20 0.67
▸ HDAC3 O15379 7/20 0.67
▸ HDAC10 Q969S8 6/20 0.67
▸ HDAC8 Q9BY41 6/20 0.67
▸ HDAC4 P56524 5/20 0.67
▸ HDAC7 Q8WUI4 5/20 0.67
▸ HDAC11 Q96DB2 5/20 0.67
▸ HDAC5 Q9UQL6 5/20 0.67
▸ PARP1 P09874 1/20 0.55
▸ MAPT P10636 2/20 0.55
▸ ELOVL1 Q9BW60 1/20 0.54
▸ NPC1 O15118 1/20 0.53
▸ CASP3 P42574 1/20 0.53
▸ RAB9A P51151 1/20 0.53
▸ SENP7 Q9BQF6 1/20 0.53
▸ MEN1 O00255 1/20 0.53
▸ GAA P10253 1/20 0.53

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
SCHEMBL24359496 1.00 HDAC1 (0.67) HDAC1HDAC2HDAC6HDAC9HDAC3
SCHEMBL24359498 1.00 HDAC1 (0.67) HDAC1HDAC2HDAC6HDAC9HDAC3
SCHEMBL24359367 0.99 HDAC1 (0.65) HDAC1HDAC2HDAC6HDAC9HDAC3
SCHEMBL24359497 0.97 HDAC1 (0.65) HDAC1HDAC2HDAC6HDAC9HDAC3
SCHEMBL29516051 0.87 ALDH1A1 (0.66) HDAC1HDAC2HDAC6HDAC9HDAC3
SCHEMBL24359376 0.87 ALDH1A1 (0.66) HDAC1HDAC2HDAC6HDAC9HDAC3
SCHEMBL29516267 0.86 HDAC1 (0.62) HDAC1HDAC2HDAC6HDAC9HDAC3
SCHEMBL24359499 0.86 HDAC1 (0.74) HDAC1HDAC2HDAC6HDAC9HDAC3
SCHEMBL24359383 0.85 HDAC1 (0.70) HDAC1HDAC2HDAC6HDAC9HDAC3
SCHEMBL24359606 0.85 HDAC1 (0.76) HDAC1HDAC2HDAC6HDAC9HDAC3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260125650-A1 METHODS AND COMPOSITIONS FOR GENERATING HEPATOCYTES TRAILHEAD BIOSYSTEMS INC (US) 2026-05-07 — — US claimed
US-12496357-B2 Compositions and methods for treating sickle cell disease YALE UNIVERSITY (US) 2025-12-16 — — US claimed
CN-116705193-A Screening method of repositioning candidate medicine and application thereof 长沙金域医学检验实验室有限公司 2023-09-05 — — CN claimed
CN-116440129-A New application of histone deacetylase inhibitor 南通大学 2023-07-18 — — CN claimed
EP-3071040-B2 METHOD FOR SCALABLE SKELETAL MUSCLE LINEAGE SPECIFICATION AND CULTIVATION UNIV MISSOURI (US) 2022-12-28 — — EP claimed
US-20220280656-A1 COMPOSITIONS AND METHODS FOR TREATING SICKLE CELL DISEASE YALE UNIVERSITY 2022-09-08 — — US claimed
US-20260125650-A1 METHODS AND COMPOSITIONS FOR GENERATING HEPATOCYTES TRAILHEAD BIOSYSTEMS INC (US) 2026-05-07 — — US disclosed
EP-4719447-A2 METHOD TO GENERATE INDUCED RETINAL PROGENITOR CELLS AND TREATMENT USING SUCH CELLS Academia Sinica (TW) 2026-04-08 — — EP disclosed
US-12553028-B2 Method to generate induced oligodendrocyte-lineage cells and treatment using such cells ACADEMIA SINICA (TW) 2026-02-17 — — US disclosed
US-12496357-B2 Compositions and methods for treating sickle cell disease YALE UNIVERSITY (US) 2025-12-16 — — US disclosed
EP-3151920-B1 USE OF INHIBITOR OF APOPTOSIS PROTEIN (IAP) ANTAGONISTS IN HIV THERAPY SANFORD BURNHAM MED RES INST (US) 2025-08-06 — — EP disclosed
US-12324817-B2 Method of inducing dedifferentiation of somatic cells with small molecules to prepare rejuvenated mesenchymal stem cells and uses thereof Shenzhen Alpha Biopharmaceutical Co. Ltd. (CN) 2025-06-10 — — US disclosed
CN-119955891-A Epileptic disease dynamic monitoring method and system based on brain organoids 同济大学 2025-05-09 — — CN disclosed
US-20160024528-A1 SOMATIC CELL NUCLEAR TRANSFER METHODS NEW YORK STEM CELL FOUNDATION, INC. 2016-01-28 — — US disclosed
EP-2971012-A1 SOMATIC CELL NUCLEAR TRANSFER METHODS The New York Stem Cell Foundation (US) 2016-01-20 — — EP disclosed
WO-2015043621-A1 HAPLOID EMBRYOGENESIS STICHTING DIENST LANDBOUWKUNDIG ONDERZOEK (NL) 2015-04-02 — — WO disclosed
WO-2015044199-A1 HAPLOID EMBRYOGENESIS STICHTING DIENST LANDBOUWKUNDIG ONDERZOEK (NL) 2015-04-02 — — WO disclosed
WO-2014144754-A1 SOMATIC CELL NUCLEAR TRANSFER METHODS THE NEW YORK STEM CELL FOUNDATION (US) 2014-09-18 — — WO disclosed
WO-2009117831-A9 HYBRID MOLECULES HAVING MIXED VITAMIN D RECEPTOR AGONISM AND HISTONE DEACETYLASE INHIBITORY PROPERTIES THE ROYAL INSTITUTION FOR THE ADVANCEMENT OF LEARNING/MCGILL UNIVERSITY (CA) 2009-12-30 — — WO disclosed
WO-2009117831-A1 HYBRID MOLECULES HAVING MIXED VITAMIN D RECEPTOR AGONISM AND HISTONE DEACETYLASE INHIBITORY PROPERTIES THE ROYAL INSTITUTION FOR THE ADVANCEMENT OF LEARNING/MCGILL UNIVERSITY (CA) 2009-10-01 — — 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 (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-12553028-B2 Method to generate induced oligodendrocyte-lineage cells and treatment using such cells HDAC4, HDAC9, MYT1 HDAC1 9/4885HDAC2 4/4885HDAC6 30/4885
US-20220280656-A1 COMPOSITIONS AND METHODS FOR TREATING SICKLE CELL DISEASE HBB, HBG1, HBZ HDAC1 4862/4885HDAC2 4881/4885HDAC6 4643/4885
US-12496357-B2 Compositions and methods for treating sickle cell disease HBB, HBG1, HBZ HDAC1 4862/4885HDAC2 4881/4885HDAC6 4643/4885
US-20260125650-A1 METHODS AND COMPOSITIONS FOR GENERATING HEPATOCYTES WNT3A, GSK3B, GSK3A HDAC1 71/4885HDAC2 432/4885HDAC6 665/4885

“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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