SCHEMBL893154

SCHEMBL893154

c1ccc(CNCCCNCc2ccccc2)cc1

nearest known ligand 0.91

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAOA P21397 1/20 0.86
CHRM2 P08172 1/20 0.82
MEN1 O00255 1/20 0.80
KMT2A Q03164 1/20 0.80
TDP1 Q9NUW8 1/20 0.80
SIGMAR1 Q99720 4/20 0.75
GAA P10253 1/20 0.67
MAPT P10636 1/20 0.67
MPO P05164 1/20 0.60
HDAC3 O15379 2/20 0.58
HDAC1 Q13547 2/20 0.58
HDAC2 Q92769 2/20 0.58
HDAC8 Q9BY41 2/20 0.58
NCOR2 Q9Y618 2/20 0.58
DRD4 P21917 1/20 0.57
SCN8A Q9UQD0 1/20 0.56
ADH1B P00325 1/20 0.56
ADH1C P00326 1/20 0.56
ADH1A P07327 1/20 0.56
ADH7 P40394 1/20 0.56

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
SCHEMBL8023026 0.97 CHRM2 (0.86) MAOACHRM2MEN1KMT2ATDP1
Hydrochloric Acid SCHEMBL3524869 0.97 MAOA (0.82) MAOACHRM2MEN1KMT2ATDP1
Hydrochloric Acid SCHEMBL8021093 0.95 CHRM2 (0.83) MAOACHRM2MEN1KMT2ATDP1
SCHEMBL8024796 0.95 CHRM2 (0.91) MAOACHRM2MEN1KMT2ATDP1
SCHEMBL12523231 0.95 CHRM2 (0.83) MAOACHRM2MEN1KMT2ATDP1
SCHEMBL12523232 0.95 CHRM2 (0.83) MAOACHRM2MEN1KMT2ATDP1
SCHEMBL4932707 0.95 MAOA (0.95) MAOACHRM2MEN1KMT2ATDP1
SCHEMBL2639857 0.93 CHRM2 (0.95) MAOACHRM2MEN1KMT2ATDP1
SCHEMBL7015048 0.93 CHRM2 (0.95) MAOACHRM2MEN1KMT2ATDP1
SCHEMBL8025398 0.93 CHRM2 (0.95) MAOACHRM2MEN1KMT2ATDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12637439-B2 Preparation of cannabichromene and related cannabinoids BAYMEDICA, INC. (US) 2026-05-26 US claimed
US-20230063862-A1 PREPARATION OF CANNABICHROMENE AND RELATED CANNABINOIDS BAYMEDICA, INC. 2023-03-02 US claimed
EP-2114899-B1 CONTROLLED RELEASE OF ACTIVE ALDEHYDES AND KETONES FROM EQUILIBRATED DYNAMIC MIXTURES FIRMENICH & CIE (CH) 2010-09-22 EP claimed
US-20100098650-A1 CONTROLLED RELEASE OF ACTIVE ALDEHYDES AND KETONES FROM EQUILIBRATED DYNAMIC MIXTURES FIRMENICH SA (CH) 2010-04-22 US claimed
EP-2114899-A2 CONTROLLED RELEASE OF ACTIVE ALDEHYDES AND KETONES FROM EQUILIBRATED DYNAMIC MIXTURES Firmenich S.A. (CH) 2009-11-11 EP claimed
WO-2008093272-A2 CONTROLLED RELEASE OF ACTIVE ALDEHYDES AND KETONES FROM EQUILIBRATED DYNAMIC MIXTURES FIRMENICH SA (CH) 2008-08-07 WO claimed
US-12637439-B2 Preparation of cannabichromene and related cannabinoids BAYMEDICA, INC. (US) 2026-05-26 US disclosed
CN-117659017-B TRPML1/2 modulator compound, pharmaceutical composition, preparation method and application thereof 北京华益健康药物研究中心 2026-05-15 CN disclosed
CN-119570023-A Dynamic polyalkenamine compound and preparation method and application thereof 华南理工大学 2025-03-07 CN disclosed
US-12172946-B2 Compound containing diphenylmethane structure and use thereof GUANGZHOU TROJAN PHARMATEC LTD. (CN) 2024-12-24 US disclosed
CN-115043867-B Six-membered cyclic aminosilane external electron donor, preparation method and application thereof 中国科学院化学研究所 2024-11-26 CN disclosed
US-20230063862-A1 PREPARATION OF CANNABICHROMENE AND RELATED CANNABINOIDS BAYMEDICA, INC. 2023-03-02 US disclosed
CN-115043867-A Hexa-membered cyclic aminosilane external electron donor, preparation method and application thereof 中国科学院化学研究所 2022-09-13 CN disclosed
US-5856590-A HYDROGENATING 4-T-BUTYLCYCLOHEXANONE BY USING A SPECIFIC RUTHENIUM-PHOSPHINE COMPLEX AS A CATALYST IN THE PRESENCE OF A BASE TAKASAGO INTERNATIONAL CORPORATION (JP) 1999-01-05 US disclosed
US-5750804-A HYDROGENATING 3-ISOCAMPHYLCYCLOHEXANONE USING RUTHENIUM/PHOSPHINE COMPLEX CATALYST IN PRESENCE OF ALKALI METAL OR ALKALINE EARTH METAL AND AMINE BASE TAKASAGO INTERNATIONAL CORPORATION (JP) 1998-05-12 US disclosed
EP-0829463-A2 (E)-(R)-2-Alkyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)-2-buten-1-ol, process for preparing the same, and use thereof in perfume compositions Takasago International Corporation (JP) 1998-03-18 EP disclosed
US-4593098-A Piperazinone and piperazine polypeptides THE UPJOHN COMPANY (US) 1986-06-03 US disclosed
US-4534897-A Piperazinone, piperazine, 1,4-diazepin-2-one and 1,4-diazepine intermediate compounds THE UPJOHN COMPANY (US) 1985-08-13 US disclosed
US-4251438-A ANALGESICS, PSYCHOTHERAPEUTIC AGENTS THE UPJOHN COMPANY (US) 1981-02-17 US disclosed
US-4179469-A Preparation of amines UOP INC. (US) 1979-12-18 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 (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-12637439-B2 Preparation of cannabichromene and related cannabinoids CNR2, CNR1, OPRM1 MAOA 325/4885CHRM2 236/4885MEN1 1301/4885
US-12172946-B2 Compound containing diphenylmethane structure and use thereof PEPD, VIP, DNPEP MAOA 1016/4885CHRM2 4567/4885MEN1 2547/4885
US-20100098650-A1 CONTROLLED RELEASE OF ACTIVE ALDEHYDES AND KETONES FROM EQUILIBRATED DYNAMIC MIXTURES PKM, APEH, PLG MAOA 18/4885CHRM2 589/4885MEN1 4140/4885
US-20230063862-A1 PREPARATION OF CANNABICHROMENE AND RELATED CANNABINOIDS CNR2, CNR1, SQLE MAOA 111/4885CHRM2 1514/4885MEN1 932/4885

“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.