SCHEMBL17959025

SCHEMBL17959025

O=C(NO)c1ccc2c(c1)CN(S(=O)(=O)c1ccccc1)CCCO2

nearest known ligand 0.50

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ HDAC6 Q9UBN7 3/20 0.50
▸ MAPT P10636 5/20 0.47
▸ ALDH1A1 P00352 5/20 0.47
▸ LMNA P02545 4/20 0.47
▸ SMN1; SMN2 Q16637 4/20 0.47
▸ MEN1 O00255 2/20 0.47
▸ HTT P42858 2/20 0.47
▸ KMT2A Q03164 2/20 0.47
▸ RAB9A P51151 1/20 0.47
▸ HDAC1 Q13547 1/20 0.46
▸ PKM P14618 1/20 0.46
▸ PKLR P30613 1/20 0.46
▸ AKR1C3 P42330 3/20 0.45
▸ POLB P06746 1/20 0.45
▸ PTBP1 P26599 1/20 0.45
▸ GAA P10253 1/20 0.43

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
SCHEMBL17958996 0.92 HDAC6 (0.50) HDAC6MAPTALDH1A1LMNASMN1; SMN2
SCHEMBL17959010 0.85 RAB9A (0.46) HDAC6MAPTALDH1A1LMNASMN1; SMN2
SCHEMBL17958999 0.84 HDAC6 (0.51) HDAC6MAPTALDH1A1LMNASMN1; SMN2
SCHEMBL17957837 0.81 ALDH1A1 (0.55) HDAC6MAPTALDH1A1LMNASMN1; SMN2
SCHEMBL17959067 0.80 HDAC6 (0.47) HDAC6MAPTALDH1A1LMNASMN1; SMN2
SCHEMBL17959037 0.80 HDAC6 (0.60) HDAC6MAPTALDH1A1LMNASMN1; SMN2
SCHEMBL1264112 0.80 HDAC6 (0.74) HDAC6MAPTALDH1A1SMN1; SMN2MEN1
SCHEMBL17959030 0.77 GPR142 (0.58) HDAC6SMN1; SMN2MEN1KMT2ARAB9A
SCHEMBL17959031 0.77 HDAC6 (0.51) HDAC6MAPTALDH1A1LMNASMN1; SMN2
SCHEMBL17959014 0.77 HDAC6 (0.57) HDAC6ALDH1A1RAB9AHDAC1PKM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10183934-B2 Bicyclic [4,6,0] hydroxamic acids as HDAC inhibitors FORMA THERAPEUTICS, INC. (US) 2019-01-22 — — US claimed
WO-2016126726-A1 BICYCLIC [4,6,0] HYDROXAMIC ACIDS AS HDAC6 INHIBITORS FORMA THERAPEUTICS, INC. (US) 2016-08-11 — — WO claimed
US-20160221997-A1 BICYCLIC [4,6,0] HYDROXAMIC ACIDS AS HDAC INHIBITORS Valo Health, LLC 2016-08-04 — — US claimed
US-12304904-B2 Bicyclic [4,6,0] hydroxamic acids as HDAC inhibitors VALO HEALTH, INC. (US) 2025-05-20 — — US disclosed
US-20230357216-A1 BICYCLIC [4,6,0] HYDROXAMIC ACIDS AS HDAC INHIBITORS Valo Health, LLC 2023-11-09 — — US disclosed
US-11702412-B2 Bicyclic [4,6,0] hydroxamic acids as HDAC inhibitors VALO HEALTH, INC. (US) 2023-07-18 — — US disclosed
US-20210206755-A1 BICYCLIC [4,6,0] HYDROXAMIC ACIDS AS HDAC INHIBITORS VALO HEALTH, INC. 2021-07-08 — — US disclosed
US-10870645-B2 Bicyclic [4,6,0] hydroxamic acids as HDAC inhibitors VALO EARLY DISCOVERY, INC. (US) 2020-12-22 — — US disclosed
US-20190345149-A1 BICYCLIC [4,6,0] HYDROXAMIC ACIDS AS HDAC INHIBITORS Valo Health, LLC 2019-11-14 — — US disclosed
US-10407418-B2 Bicyclic [4,6,0] hydroxamic acids as HDAC inhibitors FORMA THERAPEUTICS, INC. (US) 2019-09-10 — — US disclosed
US-20190092762-A1 BICYCLIC [4,6,0] HYDROXAMIC ACIDS AS HDAC INHIBITORS FORMA THERAPEUTICS, INC. (US) 2019-03-28 — — US disclosed
US-10183934-B2 Bicyclic [4,6,0] hydroxamic acids as HDAC inhibitors FORMA THERAPEUTICS, INC. (US) 2019-01-22 — — US disclosed
WO-2016126726-A1 BICYCLIC [4,6,0] HYDROXAMIC ACIDS AS HDAC6 INHIBITORS FORMA THERAPEUTICS, INC. (US) 2016-08-11 — — WO disclosed
US-20160221997-A1 BICYCLIC [4,6,0] HYDROXAMIC ACIDS AS HDAC INHIBITORS Valo Health, LLC 2016-08-04 — — 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 (10 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-20230357216-A1 BICYCLIC [4,6,0] HYDROXAMIC ACIDS AS HDAC INHIBITORS HDAC1, HDAC2, HDAC4 HDAC6 7/4885MAPT 2635/4885ALDH1A1 1767/4885
US-10870645-B2 Bicyclic [4,6,0] hydroxamic acids as HDAC inhibitors HDAC1, HDAC2, HDAC4 HDAC6 7/4885MAPT 2635/4885ALDH1A1 1767/4885
US-10407418-B2 Bicyclic [4,6,0] hydroxamic acids as HDAC inhibitors HDAC1, HDAC2, HDAC4 HDAC6 7/4885MAPT 2635/4885ALDH1A1 1767/4885
US-20160221997-A1 BICYCLIC [4,6,0] HYDROXAMIC ACIDS AS HDAC INHIBITORS HDAC1, HDAC2, HDAC4 HDAC6 7/4885MAPT 2635/4885ALDH1A1 1767/4885
US-10183934-B2 Bicyclic [4,6,0] hydroxamic acids as HDAC inhibitors HDAC1, HDAC2, HDAC4 HDAC6 7/4885MAPT 2635/4885ALDH1A1 1767/4885
US-12304904-B2 Bicyclic [4,6,0] hydroxamic acids as HDAC inhibitors HDAC1, HDAC2, HDAC4 HDAC6 7/4885MAPT 2635/4885ALDH1A1 1767/4885
US-20190092762-A1 BICYCLIC [4,6,0] HYDROXAMIC ACIDS AS HDAC INHIBITORS HDAC1, HDAC2, HDAC4 HDAC6 7/4885MAPT 2635/4885ALDH1A1 1767/4885
US-11702412-B2 Bicyclic [4,6,0] hydroxamic acids as HDAC inhibitors HDAC1, HDAC2, HDAC4 HDAC6 7/4885MAPT 2635/4885ALDH1A1 1767/4885
US-20190345149-A1 BICYCLIC [4,6,0] HYDROXAMIC ACIDS AS HDAC INHIBITORS HDAC1, HDAC2, HDAC4 HDAC6 7/4885MAPT 2635/4885ALDH1A1 1767/4885
US-20210206755-A1 BICYCLIC [4,6,0] HYDROXAMIC ACIDS AS HDAC INHIBITORS HDAC1, HDAC2, HDAC4 HDAC6 7/4885MAPT 2635/4885ALDH1A1 1767/4885

“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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