Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL29263443

NC(CCN1CCOCC1)CSc1ccccc1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.50

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Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3CHRM1CHRM2CHRM3CHRM4ESR1ESR2GABRA1GABRB1GABRG2GBA1HRH1HTR1DHTR2AOPRD1OPRK1OPRM1SLC6A2SLC6A3TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Cadaverine Tartrate. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 1/20 0.49
ALDH1A1 P00352 3/20 0.47
MAPT P10636 2/20 0.47
KMT2A Q03164 2/20 0.47
FKBP1A P62942 1/20 0.46
KDM4E B2RXH2 1/20 0.45
NPC1 O15118 2/20 0.44
RAB9A P51151 2/20 0.44
USP2 O75604 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
BCL2L1 Q07817 2/20 0.43
LMNA P02545 1/20 0.41
CYP2C19 P33261 1/20 0.41

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
Tartaric Acid SCHEMBL31024302 1.00 HSD17B10 (0.49) HSD17B10ALDH1A1MAPTKMT2AFKBP1A
Tartaric Acid SCHEMBL30165576 1.00 HSD17B10 (0.49) HSD17B10ALDH1A1MAPTKMT2AFKBP1A
SCHEMBL25087871 0.90 HSD17B10 (0.48) HSD17B10ALDH1A1MAPTKMT2AFKBP1A
SCHEMBL376570 0.90 HSD17B10 (0.48) HSD17B10ALDH1A1MAPTKMT2AFKBP1A
Hydrochloric Acid SCHEMBL21523427 0.89 HSD17B10 (0.47) HSD17B10ALDH1A1MAPTKMT2AFKBP1A
Hydrochloric Acid SCHEMBL21523430 0.89 HSD17B10 (0.47) HSD17B10ALDH1A1MAPTKMT2AFKBP1A
SCHEMBL25424454 0.85 HSD17B10 (0.47) HSD17B10ALDH1A1MAPTKMT2AFKBP1A
SCHEMBL25424456 0.85 HSD17B10 (0.47) HSD17B10ALDH1A1MAPTKMT2AFKBP1A
Hydrochloric Acid SCHEMBL25424490 0.84 HSD17B10 (0.46) HSD17B10ALDH1A1MAPTKMT2AFKBP1A
Hydrochloric Acid SCHEMBL25424488 0.84 HSD17B10 (0.46) HSD17B10ALDH1A1MAPTKMT2AFKBP1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118139835-A Method for preparing apoptosis inducer 艾伯维公司 2024-06-04 CN claimed
CN-118139835-A Method for preparing apoptosis inducer 艾伯维公司 2024-06-04 CN disclosed