U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula 2C17H19NO3.5H2O.H2O4S
Molecular Weight 758.83
Optical Activity UNSPECIFIED
Defined Stereocenters 10 / 10
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MORPHINE SULFATE

SMILES

O.O.O.O.O.OS(O)(=O)=O.[H][C@@]12OC3=C4C(C[C@H]5N(C)CC[C@@]14[C@@]5([H])C=C[C@@H]2O)=CC=C3O.[H][C@@]67OC8=C9C(C[C@H]%10N(C)CC[C@@]69[C@@]%10([H])C=C[C@@H]7O)=CC=C8O

InChI

InChIKey=GRVOTVYEFDAHCL-RTSZDRIGSA-N
InChI=1S/2C17H19NO3.H2O4S.5H2O/c2*1-18-7-6-17-10-3-5-13(20)16(17)21-15-12(19)4-2-9(14(15)17)8-11(10)18;1-5(2,3)4;;;;;/h2*2-5,10-11,13,16,19-20H,6-8H2,1H3;(H2,1,2,3,4);5*1H2/t2*10-,11+,13-,16-,17-;;;;;;/m00....../s1

HIDE SMILES / InChI
Morphine is one of the most important and widely used opioid for the treatment of chronic and acute pain: the very wide interindividual variability in the patients’ response to the drug may have genetic derivations. Sulphate salt of morphine sold under the many brand names, one of them, DURAMORPH, which is indicated for the management of pain severe enough to require use of an opioid analgesic by intravenous administration, and for which alternative treatments are not expected to be adequate. In addition for the epidural or intrathecal management of pain without attendant loss of motor, sensory, or sympathetic function. Morphine is a full opioid agonist and is relatively selective for the mu-opioid receptor, although it can bind to other opioid receptors at higher doses. The principal therapeutic action of morphine is analgesia. Like all full opioid agonists, there is no ceiling effect for analgesia with morphine. The precise mechanism of the analgesic action is unknown. However, specific CNS opioid receptors for endogenous compounds with opioid-like activity have been identified throughout the brain and spinal cord and are thought to play a role in the analgesic effects of this drug. Morphine has a high potential for addiction and abuse. Common side effects include drowsiness, vomiting, and constipation. Caution is advised when used during pregnancy or breast-feeding, as morphine will affect the baby.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P41145
Gene ID: 4986.0
Gene Symbol: OPRK1
Target Organism: Homo sapiens (Human)
Target ID: P41143
Gene ID: 4985.0
Gene Symbol: OPRD1
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
DURAMORPH PF

Approved Use

DURAMORPH is indicated for: the management of pain severe enough to require use of an opioid analgesic by intravenous administration, and for which alternative treatments are not expected to be adequate.For the epidural or intrathecal management of pain without attendant loss of motor, sensory, or sympathetic function.

Launch Date

1984
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
63 nM
2 mg single, intravenous
dose: 2 mg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
MORPHINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
165 nM × h
2 mg single, intravenous
dose: 2 mg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
MORPHINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
15.1 h
2 mg single, intravenous
dose: 2 mg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
MORPHINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
65%
2 mg single, intravenous
dose: 2 mg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
MORPHINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
Doses

Doses

DosePopulationAdverse events​
100 mg single, oral
Highest studied dose
Dose: 100 mg
Route: oral
Route: single
Dose: 100 mg
Sources:
healthy, adult
Health Status: healthy
Age Group: adult
Sex: unknown
Sources:
180 mg 1 times / day steady, oral
Dose: 180 mg, 1 times / day
Route: oral
Route: steady
Dose: 180 mg, 1 times / day
Sources:
unhealthy, adult
n = 152
Health Status: unhealthy
Condition: neuropathic pain
Age Group: adult
Sex: unknown
Population Size: 152
Sources:
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG



Drug as perpetrator​Drug as victim

Drug as victim

TargetModalityActivityMetaboliteClinical evidence
no
no
no
no
yes [Km 10100 uM]
yes [Km 12600 uM]
yes [Km 14150 uM]
yes [Km 18000 uM]
yes [Km 18700 uM]
yes [Km 25400 uM]
yes [Km 2600 uM]
yes [Km 3.4 uM]
yes [Km 3200 uM]
yes [Km 37400 uM]
yes [Km 380 uM]
yes [Km 4800 uM]
yes [Km 6400 uM]
yes
yes
yes
PubMed

PubMed

TitleDatePubMed
[Regulation of the central opioidergic nervous system on the emotional state of anxiety and its possible mechanisms].
1997 Jan
Butorphanol agonist effects and acute physical dependence in opioid abusers: comparison with morphine.
1998 Dec 1
Morphine inhibits human microglial cell production of, and migration towards, RANTES.
2000
The effects of intrathecal morphine encapsulated in L- and D-dipalmitoylphosphatidyl choline liposomes on acute nociception in rats.
2000 Aug
The effect of spinal ibuprofen on opioid withdrawal in the rat.
2000 Aug
Apnoea with intrathecal morphine.
2000 Dec
The development of pain-related behaviour and opioid tolerance after neuropathy-inducing surgery and sham surgery.
2000 Dec 1
Comparison of intravenous patient-controlled analgesia with tramadol versus morphine after microvascular breast reconstruction.
2000 Jul
Systemic naloxone enhances cerebral blood flow in anesthetized morphine-dependent rats.
2000 Nov 24
Enhanced spinal nociceptin receptor expression develops morphine tolerance and dependence.
2000 Oct 15
Inhaled morphine to relieve dyspnea in advanced cystic fibrosis lung disease.
2000 Sep
Downbeat nystagmus associated with intravenous patient-controlled administration of morphine.
2000 Sep
Advantages of intrathecal nalbuphine, compared with intrathecal morphine, after cesarean delivery: an evaluation of postoperative analgesia and adverse effects.
2000 Sep
mGlu5 receptors and nociceptive function II. mGlu5 receptors functionally expressed on peripheral sensory neurones mediate inflammatory hyperalgesia.
2001
Effect of dexmedetomidine on the release of [3H]-noradrenaline from rat kidney cortex slices: characterization of alpha2-adrenoceptor.
2001 Apr
Large-dose oral dextromethorphan as an adjunct to patient-controlled analgesia with morphine after knee surgery.
2001 Feb
Protein kinase C and G(i/o) proteins are involved in adenosine- and ischemic preconditioning-mediated renal protection.
2001 Feb
A single nucleotide polymorphic mutation in the human mu-opioid receptor severely impairs receptor signaling.
2001 Feb 2
Multicentre randomised controlled trial of nasal diamorphine for analgesia in children and teenagers with clinical fractures.
2001 Feb 3
Knockdown of spinal metabotropic glutamate receptor 1 (mGluR(1)) alleviates pain and restores opioid efficacy after nerve injury in rats.
2001 Jan
Contralateral but not systemic administration of the kappa-opioid agonist U-50,488H induces anti-nociception in acute hindpaw inflammation in rats.
2001 Jan
Comparison of three methods to find the vapor activity of a hydration step.
2001 Jan
Cellular and synaptic adaptations mediating opioid dependence.
2001 Jan
Circuitry underlying antiopioid actions of cholecystokinin within the rostral ventromedial medulla.
2001 Jan
Ketorolac reduces postoperative narcotic requirements.
2001 Jan
Morphine nerve paste.
2001 Jan
Prehospital management of rapid atrial fibrillation: recommendations for treatment protocols.
2001 Jan
Early serial EEG in hypoxic ischaemic encephalopathy.
2001 Jan
Randomized clinical trial of diathermy versus scalpel incision in elective midline laparotomy.
2001 Jan
Opiates, intracranial pressure, and autoregulation.
2001 Jan
Buprenorphine substitution ameliorates spontaneous withdrawal in fentanyl-dependent rat pups.
2001 Jan
Demographic and therapeutic determinants of pain reactivity in very low birth weight neonates at 32 Weeks' postconceptional Age.
2001 Jan
The combined effects of N-type calcium channel blockers and morphine on A delta versus C fiber mediated nociception.
2001 Jan
A prospective survey of patients after cessation of patient-controlled analgesia.
2001 Jan
Clonidine combined with a long acting local anesthetic does not prolong postoperative analgesia after brachial plexus block but does induce hemodynamic changes.
2001 Jan
Bupivacaine wound instillation via an electronic patient-controlled analgesia device and a double-catheter system does not decrease postoperative pain or opioid requirements after major abdominal surgery.
2001 Jan
A randomized, double-blinded comparison of intrathecal morphine, sufentanil and their combination versus IV morphine patient-controlled analgesia for postthoracotomy pain.
2001 Jan
Agmatine enhances the NADPH oxidase activity of neuronal NO synthase and leads to oxidative inactivation of the enzyme.
2001 Jan
Parental perceptions of comfort during mechanical ventilation.
2001 Jan
Sublingual morphine may be a suitable alternative for pain control in children in the postoperative period.
2001 Jan
Morphine with or without a local anaesthetic for postoperative intrathecal pain treatment after selective dorsal rhizotomy in children.
2001 Jan
Antianalgesic action of nociceptin originating in the brain is mediated by spinal prostaglandin E(2) in mice.
2001 Jan
Augmented accumbal serotonin levels decrease the preference for a morphine associated environment during withdrawal.
2001 Jan
Tonic descending facilitation from the rostral ventromedial medulla mediates opioid-induced abnormal pain and antinociceptive tolerance.
2001 Jan 1
Heroin-related deaths in Victoria: a review of cases for 1997 and 1998.
2001 Jan 1
Numerical density of mu opioid receptor expressing neurons in the frontal cortex of drug related fatalities.
2001 Jan 15
Acute thermal hyperalgesia elicited by low-dose morphine in normal mice is blocked by ultra-low-dose naltrexone, unmasking potent opioid analgesia.
2001 Jan 5
Occurrence of morphine tolerance and dependence in the nucleus paragigantocellularis neurons.
2001 Jan 5
Morphine induces short-lived changes in G-protein gene expression in rat prefrontal cortex.
2001 Jan 5
Effect of organic cations on the renal tubular secretion of pseudoephedrine in the rat.
2001 Jan-Feb
Patents

Sample Use Guides

Dosage for Intravenous Administration: Adult Dosage: The initial dose of morphine should be 2 mg to 10 mg/70 kg of body weight. Dosage for Epidural Administration: Adult Dosage: Initial injection of 5 mg in the lumbar region may provide satisfactory pain relief for up to 24 hours. If adequate pain relief is not achieved within one hour, careful administration of incremental doses of 1 to 2 mg at intervals sufficient to assess effectiveness may be given. Do not administer more than 10 mg per 24 hours. Dosage for Intrathecal Administration: Adult Dosage: Intrathecal dosage is usually 1/10 that of epidural dosage. A single injection of 0.2 to 1 mg may provide satisfactory pain relief for up to 24 hours. (Caution: this is only 0.4 to 2 mL of the 5 mg/10 mL ampul or 0.2 to 1 mL of the 10 mg/10 mL ampul of DURAMORPH). Do not inject intrathecally more than 2 mL of the 5 mg/10 mL ampul or 1 mL of the 10 mg/10 mLampul. Repeated intrathecal injections of DURAMORPH are not recommended. If pain recurs, consider consider alternative routes of administration.
Route of Administration: Other
It was evaluated the effect of morphine on the proangiogenic interaction taking place between macrophages and breast cancer cells in vitro. It was shown, that morphine prevents, in part via modulating VEGF-A expression, the pro-angiogenic interaction between macrophages and breast cancer cells. The conditioned medium (CM) from breast cancer cells co-cultured with macrophages elicited endothelial cell proliferation and tube formation. This effect was inhibited if the co-culture occurred in the presence of morphine (20 uM). Using a mouse antibody array, it was identified several angiogenesis-regulating factors differentially expressed in the CM of co-cultured cells prepared in the presence or absence of morphine (o, 10, 20 uM), amongst which interleukin (IL)-6, tumour necrosis factor (TNF)-α and vascular endothelial growth factor (VEGF)-A. VEGF was induced in both cell types by the co-culture and this was prevented by morphine in a non-naloxone reversible fashion. The effect of CM from co-cultured cells on endothelial tube formation, but not proliferation, was prevented by anti-VEGF neutralizing antibody
Name Type Language
MORPHINE SULFATE
EP   MART.   ORANGE BOOK   USP   VANDF   WHO-IP  
Common Name English
Morphine sulfate pentahydrate [WHO-DD]
Common Name English
MORPHINE SULFATE CII [USP-RS]
Common Name English
KADIAN
Brand Name English
KAPANOL
Brand Name English
MORPHINE SULFATE HYDRATE [JAN]
Common Name English
DEPODUR
Brand Name English
MORPHINAN-3,6-DIOL, 7,8-DIDEHYDRO-4,5-EPOXY-17-METHYL- (5.ALPHA.,6.ALPHA.)-, SULFATE, HYDRATE (2:1:5)
Common Name English
MORPHINE SULFATE [EP MONOGRAPH]
Common Name English
MST CONTINUS
Brand Name English
DOLCONTIN
Brand Name English
ASTRAMORPH
Brand Name English
DURAMORPH
Brand Name English
7,8-DIDEHYDRO-4,5.ALPHA.-EPOXY-17-METHYLMORPHINAN-3,6.ALPHA.-DIOL SULPHATE (2:1) (SALT) PENTAHYDRATE
Common Name English
7,8-Didehydro-4,5α-epoxy-17-methylmorphinan-3,6α-diol sulfate (2:1) (salt) pentahydrate
Common Name English
MORPHINAN-3,6-DIOL, 7,8-DIDEHYDRO-4,5-EPOXY-17-METHYL, (5.ALPHA.,6.ALPHA.)-, SULFATE (2:1) (SALT), PENTAHYDRATE
Common Name English
MORPHINE SULPHATE PENTAHYDRATE
Common Name English
MORPHINE HEMISULFATE HEMIPENTAHYDRATE
Common Name English
AVINZA
Brand Name English
MSIR
Brand Name English
MORPHINE SULFATE [VANDF]
Common Name English
MORPHINE SULFATE PENTAHYDRATE [MI]
Common Name English
MORPHINI SULFAS [WHO-IP LATIN]
Common Name English
MORPHINAN-3,6-DIOL, 7,8-DIDEHYDRO-4,5-EPOXY-17-METHYL, (5.ALPHA.,6.ALPHA.)-, SULPHATE (2:1) (SALT), PENTAHYDRATE
Common Name English
MORPHINE SULFATE [MART.]
Common Name English
EMBEDA COMPONENT MORPHINE SULFATE
Common Name English
MORPHINE SULFATE HYDRATE
JAN  
Common Name English
MORPHINE SULFATE [ORANGE BOOK]
Common Name English
MORPHINE SULFATE CII
USP-RS  
Common Name English
MORPHINE SULFATE PENTAHYDRATE
MI   WHO-DD  
Common Name English
ARYMO
Brand Name English
ORAMORPH
Brand Name English
INFUMORPH
Brand Name English
MORPHINE SULFATE [USP MONOGRAPH]
Common Name English
MORPHINE SULPHATE
Common Name English
MORPHABOND
Brand Name English
MS CONTIN
Brand Name English
MOSCONTIN
Brand Name English
MORCAP
Brand Name English
MORPHINE SULFATE COMPONENT OF EMBEDA
Common Name English
SEVREDOL
Brand Name English
MORPHINE SULFATE [WHO-IP]
Common Name English
Classification Tree Code System Code
DEA NO. 9300
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
NCI_THESAURUS C67413
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
FDA ORPHAN DRUG 18587
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
Code System Code Type Description
EVMPD
SUB22187
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY
FDA UNII
X3P646A2J0
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY
PUBCHEM
6321225
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY
SMS_ID
100000090222
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY
NCI_THESAURUS
C669
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY
EVMPD
SUB14597MIG
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY
WIKIPEDIA
Morphine sulfate
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY
DRUG BANK
DBSALT000122
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY
MERCK INDEX
m7631
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY Merck Index
WHO INTERNATIONAL PHARMACOPEIA
MORPHINE SULFATE
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY Description: White, feathery needles of a white, crystalline powder or cubical masses; odourless. Solubility: Soluble in 20 parts of water; slightly soluble in ethanol (~750 g/l) TS; practically insoluble in ether R. Category: Analgesic. Storage: Morphine sulfate should be kept in a tightly closed container, protected from light. Additional information: Morphine sulfate loses water of hydration on exposure to air and darkens in colour on prolonged exposureto light. Definition: Morphine sulfate contains not less than 98.0% and not more than 101.0% of (C17H19NO3)2,H2SO4, calculated with reference to the dried substance.
CAS
6211-15-0
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY
CHEBI
50731
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY
RS_ITEM_NUM
1448005
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY
RXCUI
30236
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY RxNorm
DAILYMED
X3P646A2J0
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY
EPA CompTox
DTXSID1048914
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY
ChEMBL
CHEMBL70
Created by admin on Fri Dec 15 15:32:13 GMT 2023 , Edited by admin on Fri Dec 15 15:32:13 GMT 2023
PRIMARY