SCHEMBL1174

SCHEMBL1174

CN1CCN(Cc2ccc(C(=O)Cl)cc2)CC1

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HDAC6 Q9UBN7 2/20 0.69
HRH3 Q9Y5N1 3/20 0.61
LMNA P02545 1/20 0.59
CHKA P35790 5/20 0.58
MC4R P32245 1/20 0.58
HDAC4 P56524 2/20 0.54
HDAC1 Q13547 2/20 0.54
BTK Q06187 1/20 0.54
HDAC3 O15379 1/20 0.54
HDAC7 Q8WUI4 1/20 0.54
HDAC2 Q92769 1/20 0.54
HDAC10 Q969S8 1/20 0.54
HDAC11 Q96DB2 1/20 0.54
HDAC8 Q9BY41 1/20 0.54
HDAC9 Q9UKV0 1/20 0.54
HDAC5 Q9UQL6 1/20 0.54
CA2 P00918 2/20 0.53
NCF1 P14598 1/20 0.53
PRMT6 Q96LA8 1/20 0.53
KCNH2 Q12809 1/20 0.50

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
Hydrochloric Acid SCHEMBL2412547 0.98 HDAC6 (0.68) HDAC6HRH3LMNACHKAMC4R
Hydrochloric Acid SCHEMBL529195 0.98 HDAC6 (0.68) HDAC6HRH3LMNACHKAMC4R
SCHEMBL16121572 0.90 CHKA (0.75) HDAC6HRH3CHKACA2NCF1
SCHEMBL28061494 0.88 HDAC6 (0.71) HDAC6HRH3LMNACHKAMC4R
SCHEMBL1482327 0.86 HDAC6 (0.69) HDAC6HRH3LMNACHKAMC4R
SCHEMBL12966235 0.86 HDAC6 (0.69) HDAC6HRH3LMNACHKAMC4R
SCHEMBL5839834 0.86 HDAC6 (0.69) HDAC6HRH3LMNACHKAMC4R
SCHEMBL65179 0.86 HDAC6 (0.69) HDAC6HRH3LMNACHKAMC4R
SCHEMBL16356429 0.86 HDAC6 (0.69) HDAC6HRH3LMNACHKAMC4R
SCHEMBL28818566 0.86 ALDH1A1 (0.61) HDAC6HRH3LMNAHDAC4HDAC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111004195-B Cabazitaxel alkalescent derivative and preparation thereof 沈阳药科大学 2022-01-28 CN claimed
CN-111004195-A Cabazitaxel alkalescent derivative and preparation thereof 沈阳药科大学 2020-04-14 CN claimed
EP-2608791-A1 A PROCESS FOR THE PREPARATION OF IMATINIB BASE Mustafa Nevzat Ilac Sanayii A.S. (TR) 2013-07-03 EP claimed
EP-1599462-B1 Process of preparing imatinib CIPLA LTD (IN) 2013-03-27 EP claimed
WO-2012026897-A1 A PROCESS FOR THE PREPARATION OF IMATINIB BASE MUSTAFA NEVZAT iLAÇ SANAYU A.Ş. (TR) 2012-03-01 WO claimed
WO-2012004801-A1 PROCESS FOR IMATINIB MESYLATE HETERO RESEARCH FOUNDATION (IN) 2012-01-12 WO claimed
US-7638627-B2 Imatinib hydrochloride; reacting N-(2-methyl-5-aminophenyl-4-(3-pyridyl)-2-pyrimidineamine with 4-(4-methyl-piperazinomethyl)benzoyl chloride; improved reduction step to simplify, increase yield, improve purity CIPLA LIMITED (IN) 2009-12-29 US claimed
US-7507821-B2 Process for preparing Imatinib CHEMAGIS LTD. (IL) 2009-03-24 US claimed
WO-2008136010-A1 A PROCESS FOR THE PREPARATION OF HIGHLY PURE IMATINIB BASE NATCO PHARMA LIMITED (IN) 2008-11-13 WO claimed
US-20060173182-A1 Process of preparing imatinib and imatinib prepared thereby CIPLA LIMITED (IN) 2006-08-03 US claimed
US-20060149061-A1 Novel process for preparing Imatinib PERRIGO API LTD. (IL) 2006-07-06 US claimed
EP-1599462-A2 PROCESS OF PREPARING IMATINIB Cipla Ltd. (IN) 2005-11-30 EP claimed
WO-2004074502-A2 A PROCESS OF PREPARING IMATINIB CIPLA LTD (IN) 2004-09-02 WO claimed
US-20260070903-A1 NOVEL PYRIDO[3,4-D]PYRIMIDIN-8-ONE DERIVATIVE HAVING PROTEIN KINASE INHIBITORY ACTIVITY, AND PHARMACEUTICAL COMPOSITION FOR PREVENTING, ALLEVIATING, OR TREATING CANCER, COMPRISING SAME KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2026-03-12 US disclosed
CN-113646307-B Pyrido [3,4-d ] pyrimidin-8-one derivatives having protein kinase inhibitory activity and pharmaceutical compositions thereof 韩国科学技术研究院 2024-07-30 CN disclosed
US-11725005-B2 Compositions and methods for inhibiting kinases INHIBIKASE THERAPEUTICS, INC. (US) 2023-08-15 US disclosed
US-5521184-A ANTITUMOR AGENTS; imatinib mesylate CIBA-GEIGY CORPORATION (US) 1996-05-28 US disclosed
EP-0677054-A1 NEW ANTIPARASITIC AGENTS RELATED TO THE MILBEMYCINS AND AVERMECTINS PFIZER INC. (US) 1995-10-18 EP disclosed
WO-1994015944-A1 NEW ANTIPARASITIC AGENTS RELATED TO THE MILBEMYCINS AND AVERMECTINS PFIZER LIMITED (GB) 1994-07-21 WO disclosed
CN-1077713-A Pyrimidine derivatives and preparation method thereof CIBA GEIGY AG (CH) 1993-10-27 CN 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-20060173182-A1 Process of preparing imatinib and imatinib prepared thereby ABL1, ABL2, MET HDAC6 622/4885HRH3 429/4885LMNA 3983/4885
US-20060149061-A1 Novel process for preparing Imatinib ABL1, ABL2, PDGFRA HDAC6 3008/4885HRH3 3511/4885LMNA 4399/4885
US-20260070903-A1 NOVEL PYRIDO[3,4-D]PYRIMIDIN-8-ONE DERIVATIVE HAVING PROTEIN KINASE INHIBITORY ACTIVITY, AND PHARMACEUTICAL COMPOSITION FOR PREVENTING, ALLEVIATING, OR TREATING CANCER, COMPRISING SAME CCNC, CKS1B, CKS2 HDAC6 344/4885HRH3 2682/4885LMNA 1065/4885
US-11725005-B2 Compositions and methods for inhibiting kinases MAP3K1, PACSIN2, MAP3K3 HDAC6 733/4885HRH3 3372/4885LMNA 2267/4885

“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.